ResearchingDreams TheFundamentals
ResearchingDreams TheFundamentals
RESEARCHING
DREAMS
The Fundamentals
Researching Dreams
Michael Schredl
Researching Dreams
The Fundamentals
Michael Schredl
Central Institute of Mental Health
Mannheim, Germany
This Palgrave Macmillan imprint is published by the registered company Springer Nature
Switzerland AG
The registered company address is: Gewerbestrasse 11, 6330 Cham, Switzerland
Preface
v
vi PREFACE
The purpose of the book is twofold. First, the methods of how to study
dreams are presented. Even though dreams are very private and could only
be elicited after awakening the sleeper, systematic ways to analyze these
dream reports have been developed. Like any other scientific method
there are pros and cons of this approach but understanding possible short-
comings is helpful for carrying out meaningful research projects. The sec-
ond aim of the book is to present a comprehensive introduction into the
research findings obtained so far, for example, factors of dream recall, the
continuity hypothesis of dreaming, the relationship between physiology
and dream content, etiology and therapy of nightmares, and lucid dream-
ing. The results of these studies show that studying dreams is as fascinating
as dreams themselves. The main goal of the book is achieved if the reader
is fully motivated to do dream research understanding that by using the
proper methods it can be done.
1 Definitions 1
References 7
2 Dream Recall 11
2.1 Introduction 11
2.2 Models of Dream Recall 12
2.3 Measuring Dream Recall Frequency 14
2.4 Dream Recall Frequency: Age and Gender Effects 17
2.5 Trait Factors Affecting Dream Recall Frequency 19
2.6 State Factors Affecting Dream Recall Frequency 22
2.7 An Integrative Model of Dream Recall 26
References 28
vii
viii Contents
7 Nightmares 147
7.1 Definitions147
7.2 Other Nocturnal Phenomena Associated with Negative
Emotions148
7.3 Nightmares and Sleep Quality149
7.4 Nightmare Frequency149
7.5 Nightmare Content151
7.6 Factors Affecting Nightmare Frequency152
7.7 Therapy154
References 157
8 Lucid Dreaming 163
8.1 Definitions163
8.2 Frequency of Lucid Dreaming and Its Correlates164
8.3 Lucid Dreaming Induction165
8.4 Content of Lucid Dreams167
8.5 Lucid Dreaming in the Laboratory167
8.6 Applications of Lucid Dreaming169
References 170
9 Functions of Dreaming 175
References 179
References 183
Index 223
List of Tables
xi
xii List of Tables
Definitions
Definition
Before looking more deeply into the problem regarding an exact defini-
tion of dreaming, it should be made clear that it is important to differenti-
ate between the physiological level (sleep) and the psychological level
(dreaming); some authors used dream sleep and rapid eye movement
(REM) sleep interchangeably, for example, William Dement (1960) chose
the title “The effect of dream deprivation” for his study which aimed at
deprivation of REM sleep and not dream deprivation. Keeping these two
levels apart is crucial for theories about dream function(s) compared to
functions of REM sleep (see Chap. 9). It is also important regarding a
possible taxonomy of dreams as subjective experiences in contrast to the
classification of brain states with physiological measures like electroen-
cephalogram (EEG) or imaging (wakefulness, REM sleep, NREM sleep,
slow wave sleep, etc.). For example, are REM dreams qualitatively differ-
ent from non-rapid eye movement (NREM) dreams or is this idea of clas-
sification mixing up the criteria for REM sleep and NREM sleep (American
Academy of Sleep Medicine 2007) with a classification of subjective expe-
riences that might be affected by the underlying brain state but also show
a considerable overlap in phenomenological characteristics if obtained
from different brain states, for example, daydreaming and experiences
under the influence of hallucinogenic drugs, useful?
The phenomenology of dreaming—if recalled—has been described by
many authors (for a review see: Windt 2015). Typically the dream experi-
ences are perceived as real as waking-life experiences while dreaming (with
the exception of lucid dreaming; although even in these dreams the experi-
ences are real [sometimes more intense and detailed] despite the knowledge
that it is a dream) and several analogues have been suggested over the years,
for example, dreaming has similarities to viewing a film (Cook 2011), dream-
ing as a form of virtual reality (Hobson and Schredl 2011), dreaming as an
organic psychosis with hallucinations and delusions (Hobson and Voss 2011),
dreams as immersive spatiotemporal hallucinations (Windt 2015), or dreams
as a world simulation (Revonsuo et al. 2015). The question is whether these
descriptions are helpful in understanding dreaming. The analogy between
film viewing and dreaming seems difficult, for example, there is still a discus-
sion ongoing whether dreams can be black-and-white like films in the
black-and-white area (König et al. 2017). Hallucinations are defined in a
psychiatric context as perception-like experiences that occur without an
external stimulus (American Psychiatric Association 2013). The term halluci-
nation might be an analogue for the visual, auditory, and other sensory
impressions while dreaming but is not very adequate to describe the
DEFINITIONS 3
very likely that the dream reflects the experiences that occurred during
sleep. Similarly, the correlations between physiological parameters mea-
sured during sleep and the dream report obtained after awakening do not
support the idea that dream reports are generated during the awakening
process (see Chap. 5). If, for example, muscle twitches during sleep cor-
relate with dream actions or heart rate increases minutes before being
woken up by a nightmare, these reported experiences must have occurred
during sleep. Sleep talking has also been related to dream content (Arkin
et al. 1970) and patients with REM sleep behavior disorder act out their
dreams, observed movements are in sync with the remembered actions
after waking up (Valli et al. 2012). Similar, lucid dream research is provid-
ing evidence for the notion that dreaming is taking place during sleep,
proficient lucid dreamers can perform eye movements within the lucid
dream that can be measured via the electrooculogram and even communi-
cate with the experimenter via Morse code; the experimenter uses two
different tones and the lucid dreamer can react with different eye move-
ment patterns (Appel and Pipa 2017). Taking together these lines of
research, the evidence is clearly in favor of the assumption that dreams are
subjective experiences during sleep and that the dream report is a recollec-
tion of these experiences. Whether the dream report is an accurate account
of the dream experiences is an important topic discussed in Chap. 3 within
the context of dream content analysis. If the dreamer, for example, focuses
on reporting only the dream action but not the accompanying thoughts
and emotions, findings based on such reports might yield a biased picture
of what dreaming is like. Therefore, researchers (Kahan 2012; Nielsen
2000a) strongly recommend to train participants regarding their skills of
dream reporting.
The question whether all remembered sleep experiences reported upon
awakening should be considered as dreams had a strong impact on the
REM-NREM debate that started after the discovery of REM sleep in
1953 (Montangero 2018). In the first sleep laboratory studies (e.g.,
Aserinsky and Kleitman 1953) the participants were asked about dreams
after they were awakened, resulting in high recall rates after REM awaken-
ings and very low recall rates after NREM awakenings. Foulkes (1962)
changed the question to “What was going through your mind before I
woke you up?” and obtained much higher recall rates for NREM awaken-
ings because he obtained reports that are thought-like but did not include
images. So, some researchers (e.g., Nielsen 2000b) used the term “sleep
mentation” for describing all possible experiences that can be recalled
DEFINITIONS 5
from sleep and “dream” only for reports including a temporal progression
with images, thoughts, emotions, and so on (i.e., a full story like a recall
of a waking-life experience). In one paper even the term “dreamless sleep
experiences” was introduced (Windt et al. 2016), but this notion seems to
complicate matters even more. In order to illustrate this topic of differen-
tiating between different types of sleep-related experiences, several dream
examples of the NREM awakening study of Schredl, Brennecke, and
Reinhard (2013) will be presented. Overall, 12 participants reported 52
dreams (dream report length ranged from 4 to 163 words); the recall rate
was about 60%.
The following report could be classified as thought-like: “I was think-
ing about the possibility that the experimenter will soon awaken me.” The
report “There was an animal.” might include some perceptual qualities,
whereas a report like “I was sitting with another person in a car. We were
talking. It was during the day.” clearly includes perceptions (visual, audi-
tory) and is a world simulation. Classifying all 52 reports, only 3 reports
were clearly thought-like, 5 reports were ambiguous, but the majority of
the reports (N = 45)—even though they were much shorter than REM
dream reports (e.g., Schredl et al. 2009)—clearly were “dream-like”.
Nielsen (2000a) suggested to use those brief dreams with one setting the
term “minimal dreaming” but the major question is whether these brief
dream reports might be short because it is more difficult for the dreamer
to remember more sequences after being woken up from NREM sleep
compared to be awakened from REM sleep. The reanalysis of the data of
Schredl, Brennecke, et al. (2013) indicates that the distinction “thought-
like” versus “dream-like” does not help to differentiate between NREM
and REM dreams on a qualitative level (see also: Antrobus 1983). So, the
question arises whether it is helpful to classify sleep-related experiences in
qualitative distinctive categories. The suggestion put forward in this book
is to term all reports that reflect sleep-related experiences as “dreams”
(reflecting dreaming) and be aware of the range of experiences that can
occur, from thought-like reports to very intense nightmares. Waking-life
experiences show the similar range, for example, from “I was just thinking
about the talk I have to give tomorrow” to scenarios with strong emotions
like falling in love.
Another interesting question was addressed by Nielsen (2000a): Are
there cognitive activities during sleep that cannot be reported—despite all
possible introspective effort? This question is of special interest regarding
sleep-dependent memory consolidation which assumes that brain-activation
6 M. SCHREDL
patterns that occurred during the learning phase are reactivated during
sleep (Zhang et al. 2017). As during wakefulness the brain is processing a
lot more information than reflected in the consciousness of the persons, it
seems plausible that the sleeping brain is also doing a lot more than “just”
dreaming. For example, long-term potentiation altering the coupling
between neurons which is involved in sleep-dependent memory consolida-
tion (Ribeiro and Nicolelis 2004) or pruning (reducing the number of
synapses during slow wave sleep) (Tononi and Cirelli 2001) is presumably
not accompanied by conscious perceptions or related subjective experi-
ences. Nevertheless, dreaming might also reflect—at least partly—these
memory consolidation processes during sleep (Wamsley 2014).
If waking thoughts were collected under similar conditions (dark room,
lying in a bed, “awakened” by an experimenter via intercom), the report of
these waking experiences can be dream-like, for example, include bizarre
elements (Foulkes and Fleisher 1975). That is, from a phenomenological
viewpoint there is considerable overlap between daydreaming, mind wan-
dering, and dreaming (Starker 1978). The major difference, of course, is
that the brain is in a different state (waking vs. sleeping). But even that
distinction might be arbitrary as mind wandering and dreaming might
share the same neuronal substrate, the default network (Fox et al. 2013),
that is, there is also a marked overlap regarding the involved brain net-
works. Also during other brain states dream-like experiences can occur, for
example, during anesthesia (Hellwagner et al. 2003) or taking drugs like
LSD (Kraehenmann et al. 2017). Whether it is helpful to name these expe-
riences as dreaming is doubtful. Even closer to dreaming—defined as sub-
jective experiences during sleep—are the subjective experiences while sleep
walking (Oudiette et al. 2009), but it should be kept in mind that sleep
walking is a NREM parasomnia also called disorder of arousal which is
characterized by a brain state that is neither fully asleep nor fully awake,
that is, simple tasks like walking with open eyes work but more complex
cognitive tasks like recognizing faces are impeded (American Academy of
Sleep Medicine 2014). If sticking to the exact definition of dreaming given
above, the subjective experiences of sleepwalkers should not be termed
“dreaming” as the brain state is not “sleep” but an intermediate state.
Another phenomenon that is not easy to differentiate from dreaming is the
experiencing of persons with sleep state misperception, or “paradoxical
insomnia” (American Academy of Sleep Medicine 2014). These patients
think that they are awake even though the standard polysomnographic
recording with EEG, electrooculogram (EOG), and electromyogram
(EMG) shows sleep—according to the international classification rules for
DEFINITIONS 7
References
American Academy of Sleep Medicine. (2007). The AASM manual for the scoring
of sleep and associated events: Rules, terminology, and technical specifications.
Westchester: American Academy of Sleep Medicine.
American Academy of Sleep Medicine. (2014). The international classification of
sleep disorders (ICSD-3). Darien: AASM.
American Psychiatric Association. (2013). Diagnostic and statistical manual of
mental disorders: DSM-5. Washington, DC: American Psychiatric Association.
Antrobus, J. S. (1983). REM and NREM sleep reports: Comparison of word fre-
quencies by cognitive classes. Psychophysiology, 20, 562–568.
Appel, K., & Pipa, G. (2017). Auditory evoked potentials in lucid dreams: A dis-
sertation summary. International Journal of Dream Research, 10(1), 98–100.
Arkin, A. M., Toth, M. F., Baker, J., & Hastey, J. M. (1970). The degree of con-
cordance between content of sleep talking and mentation recalled in wakeful-
ness. Journal of Nervous and Mental Disease, 151, 375–393.
Aserinsky, E., & Kleitman, N. (1953). Regularly occurring periods of eye motility
and concomitant phenomena during sleep. Science, 118, 273–274.
Cook, R. F. (2011). Correspondences in visual imaging and spatial orientation in
dreaming and film viewing. Dreaming, 21(2), 89–104.
8 M. SCHREDL
Oudiette, D., Leu, S., Pottier, M., Buzare, M.-A., Brion, A., & Arnulf, I. (2009).
Dreamlike mentations during sleepwalking and sleep terrors in adults. Sleep, 32,
1621–1627.
Revonsuo, A., Tuominen, J., & Valli, K. (2015). The simulation theories of dream-
ing: How to make theoretical progress in dream science. In T. K. Metzinger &
J. M. Windt (Eds.), Open mind (pp. 1–8). Frankfurt am Main: Mind Group.
Ribeiro, S., & Nicolelis, M. A. L. (2004). Reverberation, storage, and postsynaptic
propagation of memories during sleep. Learning and Memory, 11, 686–696.
Schredl, M., Atanasova, D., Hörmann, K., Maurer, J. T., Hummel, T., & Stuck,
B. A. (2009). Information processing during sleep: The effect of olfactory
stimuli on dream content and dream emotions. Journal of Sleep Research, 18,
285–290.
Schredl, M., Brennecke, J., & Reinhard, I. (2013). Does training increase NREM
dream recall? A pilot study. International Journal of Dream Research, 6, 54–58.
Starker, S. (1978). Dreams and waking fantasy. In K. S. Pope & J. L. Singer (Eds.),
The stream of consciousness (pp. 301–319). New York: Plenum.
Tart, C. T. (1987). The world simulation process in waking and dreaming: A sys-
tems analysis of structure. Journal of Mental Imagery, 11, 145–157.
Tononi, G., & Cirelli, C. (2001). Some considerations on sleep and neural plastic-
ity. Achives Italiennes de Biologie, 139, 221–241.
Valli, K., Frauscher, B., Gschliesser, V., Wolf, E., Falkenstetter, T., Schönwald,
S. V., Ehrmann, L., Zangerl, A., Marti, I., Boesch, S. M., Revonsuo, A., Poewe,
W., & Högl, B. (2012). Can observers link dream content to behaviours in
rapid eye movement sleep behaviour disorder? A cross-sectional experimental
pilot study. Journal of Sleep Research, 21, 21–29. [Link]
org/10.1111/j.1365-2869.2011.00938.x.
Wamsley, E. J. (2014). Dreaming and offline memory consolidation. Current
Neurology and Neuroscience Reports, 14(3), 1–7.
Windt, J. M. (2015). Dreaming – A conceptual framework for philosophy of mind
and empirical research. Cambridge, MA: MIT Press.
Windt, J. M., Nielsen, T., & Thompson, E. (2016). Does consciousness disappear
in dreamless sleep? Trends in Cognitive Sciences, 20(12), 871–882.
Zhang, H., Deuker, L., & Axmacher, N. (2017). Replay in humans—First evi-
dence and open questions. In N. Axmacher & B. Rasch (Eds.), Cognitive neu-
roscience of memory consolidation (pp. 251–263). Cham: Springer.
CHAPTER 2
Dream Recall
2.1 Introduction
As pointed out in Chap. 1, the hypothesis that the mind never sleeps is
widely accepted, that is, some form of experiencing (emotions, thoughts,
mental images, etc.) is present during every single minute of sleep. Despite
this assumption that every person dreams every night, the variability of
dream recall in the home setting is considerably large. Some persons
almost never recall any dream, whereas others can relate a detailed descrip-
tion of their nightly experiences almost every morning. As successful
dream recall is a prerequisite for dream research (and for the clinical use of
dreams), this chapter focuses on this topic, starting with a simple defini-
tion, and reviews the dream recall models, the methods how to measure
dream recall frequency (DRF), and the factors (state and trait factors)
affecting DRF. An attempt to formulate a comprehensive model of dream
recall is the topic of the last section of this chapter.
Dream recall can be defined as follows (Schredl 2007):
A topic that has been addressed already in Chap. 1 is the question that
how does one know that the dream report remembered after awakening is
a recollection of experiences that occurred during sleep and not produced
in milliseconds during the awakening process. Research in lucid dreaming
(see Chap. 8) and application of external stimuli that affect dream content
(see Chap. 4) indicate that the assumption that dream reports reflect
dreaming (subjective experiences during sleep) is very, very plausible.
model, the process of retrieval, is important. The more salient the dream
experience and the less interferences occur during the retrieval process,
the higher is the probability of recalling the dream. Even the repression
hypothesis was integrated into the model, that is, very intense emotions
might also result in a smaller chance of recalling the dream.
The functional state-shift model of dream recall was formulated by
Koukkou and Lehmann (1983). Within this model cognitive activation of
the brain is divided into different functional states with their associated
memory storages. Higher functional states cannot very easily access mem-
ory storage system of a lower functional state, whereas the information
flow in the other direction is good. This explains why waking-life elements
are reflected in dreams (REM sleep is a functional state which is lower in
activation than the waking state) but waking consciousness has limited
access to the contents of the REM sleep periods. In the dream recall pro-
cess the transfer of experiences occurring in the functional state of REM
or NREM sleep would be easier if the difference in terms of overall brain
activation between the sleep state and the waking state was closer. A sim-
ple prediction would be that dream recall is lower after awakening from
NREM sleep compared to REM sleep, or awakenings during the second
part of the night are more likely produce dream recall than awakenings at
the beginning of the night as the brain is more active. The concept of a
general brain activation seems a bit outdated as imaging studies have
shown that brain activation patterns during sleep are quite complex
(Hobson et al. 2000).
One should keep in mind that these six theories or models do not
exclude each other; it may be that each theory captures a specific impor-
tant aspect of recalling a dream.
Table 2.2 Rating scale measuring dream recall frequency (DRF) (Schredl 2004a)
How often have you recalled your dreams recently (several months)?
Göritz 2015). These high coefficients indicate that this scale measures
inter-individual differences reliably.
Within the dream diary approach two types of diaries were used: Either
the participants should simply state each morning whether they have
dreamt or not (checklist), or they should—for content analytic studies—
record the dream(s) of the previous night as completely as possible (narra-
tive dream diary). From a methodological viewpoint, checklists are better
than narrative diaries as the recording of dreams each morning yielded a
decrease in DRF after one week (Schredl 2004b; Zadra and Robert 2012).
For a checklist study there was no drop in dream recall even after 12 weeks
(Schredl and Fulda 2005b). In order to measure inter-individual differ-
ences reliably, a high internal consistency of the diary had to be obtained in
the sample (the analogy is a psychometric test; the internal consistency
increases with the number of items and, here, the “item” is a Yes or No
answer each morning regarding dream recall). Using a checklist in a sample
of 198 participants, the internal consistency (Cronbach’s alpha) increased
with duration: r = 0.677 (7 days), r = 0.818 (14 days), r = 0.876 (21 days),
and r = 0.904 (28 days) indicating that a two-week diary typically will yield
sufficient reliability (Schredl and Fulda 2005b). For a two-week narrative
diary, the internal consistency was r = 0.743 (Schredl et al. 2003).
In general, the correlation coefficients between DRF measured via
questionnaire scale (retrospective measure) and DRF via dream diary
(prospective measure) are of moderate size: r = 0.69, N = 338 (Cohen
1979), r = 0.52, N = 336 (Hill et al. 1997), r = 0.557, N = 285 (Schredl
2002), and r = 0.562, N = 444 (Schredl et al. 2003). Whereas these cor-
relations are sufficiently large, the problem is a big discrepancy regarding
the amount of dream recall. Cohen (1969), for example, reported a three-
16 M. SCHREDL
fold increase in DRF and a recent study (Zunker et al. 2015) found an
increase of 3.75 ± 2.58 mornings per two weeks with dream recall (ques-
tionnaire) to 6.93 ± 2.80 mornings per two weeks (checklist diary), this
equals a large effect size of d = 1.07. The increase in dream recall was
much more pronounced for low dream recallers than for high dream
recallers (Schredl 2002). Even a simple encouragement (Halliday 1992;
Redfering and Keller 1974) or filling out a dream questionnaire (Schredl
et al. 2002) can increase DRF considerably.
Given the marked differences between retrospective and prospective
measures, the question arises as to how these differences can be explained.
Aspy, Delfabbro, and Proeve (2015) outlined two possible explanations:
underestimation of the retrospective measures and enhancement effects of
the diary measures. The fact that the retrospective measures—asking for
estimations about the last 12 months—yielded lower figures than estimates
for a one-month interval would support this idea that successful dream
recall might simply be forgotten. Another hypothesis is that retrospective
measures might be biased by personality dimensions (Beaulieu-Prevost and
Zadra 2005; Bernstein and Roberts 1995) as personality measures, for
example, absorption, thin boundaries, showed higher correlations with ret-
rospectively measured dream recall when compared to figures obtained
from diary measures (Beaulieu-Prevost and Zadra 2005). In addition to
reliability issues (lower reliability of diary measures), the assumption is that
persons who are not interested in dreams (associated with low absorption,
thick boundaries) tend to underestimate their dream recall systematically.
The other line of thinking focuses on the recall-enhancing effects of
keeping a dream diary, that is, the intention to recall a dream might mini-
mize interferences during the awakening process (Aspy et al. 2015).
Interestingly, Zadra and Robert (2012) found a higher increase from ret-
rospective estimates of dream recall in the first five days of keeping a nar-
rative dream log (including recording the dreams which can take a lot of
time) compared to a checklist dream log (just filling in whether there was
a dream (or several dreams) or not). As the increase in dream recall by
keeping a diary is significantly related to a positive attitude toward dreams
(Zadra and Robert 2012), the idea that motivation might play a role in the
dream diary enhancement effect seems very plausible.
As a measure of “true” DRF is not available, one has to keep in mind
that retrospective measures might underestimate DRF whereas prospective
measures produce overestimations due to focusing the attention of the
participants on dream recall.
DREAM RECALL 17
Table 2.3 Gender differences in dream recall—a meta-analysis: effect sizes for
different age groups (Schredl and Reinhard 2008b)
Age group Studies Females/ Estimated Confidence
Males effect size interval (95%)
Genetic factors
Personality factors
Repression, neuroticism, introversion, openness to experience, absorption, “thin”
boundaries
Cognitive factors
Intelligence, memory, fantasy, creativity
Sleep behavior
Sleep and waking physiology
Attitude toward dreams
20 M. SCHREDL
genetic influence on dream recall. These findings with relatively small sam-
ple sizes did not support the presence of a genetic effect. Cohen (1973)
reported that the concordance rates in dream recall (similar high or low
DRF) were high for persons who live together independent of their shared
genetic background. Genome-wide association studies (GWAS) have not
yet been carried out.
Based on Freud’s repression hypothesis (see Table 2.1) researchers
investigated the relationship between the personality trait sensitizer versus
repressor (subscale of the Minnesota Multiphasic Personality Inventory;
MMPI) in relation to dream recall. Repressors are persons who avoid pos-
sibly threatening stimuli and/or deny their existences. Sensitizers, on the
other hand, are persons who focus on possibly threatening stimuli and pay
attention to them. Tart (1962) found—as expected—a negative correla-
tion between this dimension (high scores represent sensitization) and
DRF: r = −0.25 (p < 0.05, N = 45). Subsequent studies, however, did not
yield a homogeneous picture; the majority of research findings did not
reveal a substantial relationship between this or similar personality dimen-
sions and DRF (Schredl 2007).
More promising were dimensions like “thin boundaries” (Hartmann
1991), “hypnotic ability” (Belicki and Bowers 1982), and absorption
(Schredl et al. 1997; Spanos et al. 1980). These dimensions show high cor-
relations with the openness to experience factor of the Big Five Personality
model (McCrae 1994). In student samples, small correlations between
openness to experience and DRF were found (Blagrove et al. 2003; Hill
et al. 1997; Schredl et al. 2003; Watson 2003). These findings were con-
firmed in a large sample (N = 2,492 with a more diverse educational back-
ground and a large age range of 17–93 years) (Schredl and Göritz 2017).
The alexithymia construct (affective deficits, lack of introspection) seems to
reflect the other end of the openness dimension and was inversely related
to DRF in several studies (De Gennaro et al. 2003; Nielsen et al. 1997;
Parker et al. 2000). The other four factors of the Big Five model are not
strongly associated with dream recall, except a small—yet unexplained—
correlation to conscientiousness and a small correlation to neuroticism
which was no longer significant if nightmare frequency was statistically
controlled (Schredl and Göritz 2017), that is, nightmare frequency is
related to neuroticism (see Chap. 7) and this increases overall DRF.
General intelligence or verbal intelligence was not significantly related
to DRF (Schredl 2007), more promising are the findings regarding visual
memory—persons with high scores tend to recall their dreams more often,
DREAM RECALL 21
especially in the elderly (Cory et al. 1975; Schredl et al. 1996; Waterman
1991). Other forms of memory such as verbal memory and short-term
memory in general were rarely connected to DRF (Blagrove and Akehurst
2000). Another interesting link was found between dream recall and auto-
biographical memory (Horton and Malinowski 2015). Visual imagina-
tion, pronounced fantasy life, creativity, and the frequency of daydreaming
correlated with DRF (Schredl 2007); this makes sense as these aspects are
likely to be associated with the openness to experience factor.
As long sleepers (8–10 hours’ sleep duration) have more REM sleep
than short sleepers (cf. Cartwright 1978) and recall rates are higher after
awakenings from REM sleep compared to NREM sleep (Hobson and
Stickgold 1994), it was hypothesized that habitual sleep duration was
related positively with dream recall. Interestingly, two diary studies
(Schredl and Fulda 2005a; Schredl and Reinhard 2008a) analyzing the
effect of the between-subject factor (habitual sleep duration) and the
with-subject factor (short-term changes in sleep duration) clearly indicate
that the sleep duration plays a minor role in explaining inter-individual
differences in dream recall but the short-term changes in sleep duration
had marked effects on dream recall, that is, if one night a person sleeps
considerably shorter than she/he usually sleeps, then dream recall is mark-
edly reduced. Poor sleep quality and frequent nocturnal awakenings are
associated with DRF, a finding that might simply be explained by an
increased chance to recall a dream after awakening if frequency of the
awakenings is higher (Schredl et al. 2003).
Using Positron Emission Tomography (PET) combined with EEG,
Eichenlaub et al. (2014) found that the 21 high dream recallers (more
than three dreams per week) showed higher regional cerebral blood flow
(rCBF) in temporoparietal junction (TPJ) during REM sleep, slow wave
sleep, and wakefulness, and also increased regional cerebral blood flow
(rCBF) in the medial prefrontal cortex (MPFC) during REM sleep and
wakefulness than low dream recallers (less than two per month). As these
brain areas are part of the resting state network which is associated with
mind wandering (daydreaming) during wakefulness and dreaming (Fox
et al. 2013), these results suggest that the ability to recall dreaming is
associated with a trait aspect of cerebral functional organization. The brain
activation after presenting auditory stimuli during sleep (event-related
potential paradigm) was also higher in habitual high dream recallers com-
pared to low dream recallers (Eichenlaub, Bertrand et al. 2014; Vallat
et al. 2017b). In order to differentiate between state and trait aspects, it
22 M. SCHREDL
dream (Schredl and Fulda 2005a; Schredl and Reinhard 2008a), that is,
sleep duration tends to be a state factor regarding its effect on dream
recall not a trait factor. The frequency of nocturnal awakenings measured
on a day-to-day basis via a dream diary is associated with an enhanced
probability for recalling a dream the next morning (Schredl and Montasser
1996); this complements the studies reporting a relationship between
DRF and the frequency of nocturnal awakenings as a trait factor. The
results of Vallat, Lajnef, et al. (2017b) indicated that periods of wakefulness
should be two minutes or longer to facilitate dream recall.
The studies regarding the effect of EEG parameters during the REM
period prior to awakening on dream recall yielded contradictory results
(Schredl 2007). A recent study (Siclari et al. 2017) using high-density
EEG (256 electrodes) found local decreases of low-frequency activity
(reflecting more activity) in parieto-occipital areas prior to successful
dream recall after awakenings from REM sleep and NREM sleep. These
areas are active during REM sleep (Hobson et al. 2000) and dream recall
was absent if these areas were damaged (Solms 1997). The high spatial
resolution of the Siclari et al. (2017) study clearly indicates that specific
patterns of brain activity play a role in explaining successful dream
recall and not a general index of brain activation—a problem with the
original formulation of the state-shift model of dream recall (Koukkou
and Lehmann 1983). Why Siclari et al. (2017) confused successful dream
recall with the presence or absence of dreaming is not clear. Interestingly,
rhinal-hippocampal connectivity values (a parameter important for suc-
cessful memory formation) were higher in patients with good dream recall
versus those patients with poor dream recall, underpinning the notion that
dream recall is a memory process (Fell et al. 2006).
A clear relationship between physiological activity during REM sleep,
for example, heart rate, skin conductance (as a measure for emotional
salience), could not be demonstrated (Schredl and Montasser 1996); this
might be simply explained by the inhomogeneous findings regarding the
emotional intensity of the dream and autonomic parameters (Schredl
2008b).
Cohen and Wolfe (1973) tested whether interferences during or shortly
after the awakening process impair dream recall. One group of participants
were asked to call the weather forecast upon awakening (duration: two to
three minutes), whereas the other group lay quietly in their beds for the
same amount of time. As expected, the interference of calling the weather
forecast impaired dream recall (29% vs. 54%). However, a diary study
(Schredl and Montasser 1996) carried out in the home setting did not
DREAM RECALL 25
reveal any effect of interferences, for example, talking to the bed partner,
on dream recall. As the intention to recall a dream can increase dream
recall (see above; effects of keeping a dream diary), it would be very inter-
esting to study possible effects of internal interferences, for example,
thoughts about the upcoming schedule or thinking about current con-
cerns, on dream recall. Vallat, Meunier, Nicolas, and Ruby (2017c) investi-
gate another factor that might impede dream recall: the so-called sleep
inertia. After waking up, the brain is not fully functional compared to alert
wakefulness, for example, memory capacity might be decreased (Trotti
2017). This sleep inertia effect seems to be less pronounced in high dream
recallers compared to low dream recallers (Vallat et al. 2017c). Whether
sleep inertia is a state factor affecting dream recall or a trait factor (or
both) is yet to be seen.
Patients with mental disorders that are accompanied with cognitive
impairment like severe depression or dementia are showing lower DRF
compared to healthy controls (Kramer et al. 1975; Riemann et al. 1990).
Brain lesions within the parietal-occipital junction which is often associ-
ated with loss of spatial perception results in a cessation of dream recall
(Solms 1997). Also, large lesions in the frontal areas can cause complete
inability to remember dreams indicating those areas are crucial for dream
recall (Solms 1997). Interestingly, most patients recovered over a period
of one year and began to remember dreams again (Murri et al. 1989)—an
indication of the brain’s plasticity.
The treatment with the tricyclic antidepressant trimipramine was
accompanied by a slight decrease in DRF in a large sample of outpa-
tients, most likely explained by a shift toward more positive dream emo-
tions and a decrease in nightmares (Schredl et al. 2009), that is, it may
not be a direct effect. Other studies also point in the direction of dream
recall reducing effect of tricyclic antidepressants (see review: Tribl et al.
2013) whereas serotonin-reuptake inhibitors or similar compounds did
not show a systematic effect on dream recall, only in healthy controls
dream recall was reduced by serotonin-reuptake inhibitors (Pace-Schott
et al. 2001). It seems plausible that the effects of these drugs on the
amount of REM sleep (most antidepressants suppress REM sleep, not so
trimipramine) may explain alterations in DRF, but the findings of
Armitage Schredl, Riemann, et al. (2009) indicate that other factors may
play a role as well.
26 M. SCHREDL
Duration
Sleep inertia
Short-term Long-term
Dreaming Dream report
memory memory
Interferences Salience
Salience
Focusing on dreams/Memorizing Report style (verbal/ written)
Personality/Interest in dreams
Daytime experiences
state factors, for example, the higher recall rates from REM sleep compared
to those after NREM sleep awakenings (Nielsen 2000) and the effect that
shorter sleep duration within an individual is associated with a lower prob-
ability to recall a dream, as sleep inertia is more pronounced if sleep duration
is markedly below the individual’s mean sleep duration (Trotti 2017). The
effect of the duration of the awakenings process is often reported by persons
who tried to recall their dream in the home setting; at the moment of awak-
ening the dream is remembered but if the person continues to sleep, the
dream is gone. A duration of at least two minutes wakefulness seems to be
crucial for successfully transferring the dream from short-term memory into
long-term memory (Vallat et al. 2017b). The importance of the last step
(long-term memory—dream report) is evident in the findings that cues can
improve recall are considered (Botman and Crovitz 1989). An object seen
during the day can trigger the recall of a dream including the same topic
(Domhoff 1969), that is, even if the dream is not remembered immediately
after awakening, it might lie dormant in the long-term memory system—
according to Koukkou and Lehmann (1983), in the memory system of the
functional state “Sleep” that is not easily accessible from the functional state
“Waking”. Observations that proficient lucid dreamers can remember previ-
ous lucid dreams (Tholey and Utecht 1987) would fit in this line of think-
ing. The arousal-retrieval model of Koulack and Goodenough (1976) and
the state-shift model of Koukkou and Lehmann (1983) capture at least part
of these effects of physiology on dream recall but many questions are still
unresolved, for example, the interaction between physiological and psycho-
logical variables (e.g., personality).
The most general psychological variables are trait factors like personality
dimensions (openness to experience, thin boundaries, etc.). The effects fit
with the life-style hypothesis of Schonbar (1965). However, the question
arises how these personality dimensions might affect the recall process dur-
ing awakening. Several pathways are possible (not excluding each other),
for example, creative persons experience more intense dreams (salience
hypothesis) that are easier to recall, and persons who are interested in
dream might focus during the time they wake up on recalling the dream
and thus minimizing interferences (interference hypothesis), or creative
persons might have a more functional default network (also related to day-
dreaming) and therefore are able to recall their dreams better. Testing these
hypotheses is the mission of future research. The effect of state factors
would also fit in this concept; stressful periods are accompanied with more
28 M. SCHREDL
salient dreams (and often also with more awakenings during sleep) that are
more easily remembered, but one might imagine that interferences during
the awakening process might also be stronger as stressful thoughts might
pop into mind immediately after awakening—see the differential effect of
stress on dream recall in men and women (Armitage 1992). The enhance-
ment effect of keeping a dream diary or participating in a dream study on
dream recall might be explained by focusing on the dream experiences dur-
ing awakening (reducing interferences) and even increase the transfer rate
by memorizing the dream in this period. An important factor of method-
ological relevance is the effect of salience on dream reporting within the
most recent dream approach. Even though the dream was remembered
successfully in the morning, days or weeks later mundane dreams might be
forgotten but bizarre, funny, or salient dreams are reported—representing
a selection bias regarding dream salience. Similarly, the report style (how
detailed a dream is reported or recounted) might be associated with per-
sonality, for example, creativity, and thus affect the findings obtained by the
dream content analysis method. As reported above, controlling for dream
length seems a crucial measure to counter such influences.
To summarize, despite the considerable number of studies investigating
successful dream recall (the prerequisite to do dream research), many
questions regarding the interaction of physiological and psychological fac-
tors are still unanswered.
References
Aarons, L. (1976). Sleep-assisted instruction. Psychological Bulletin, 83, 1–40.
Armitage, R. (1992). Gender differences and the effect of stress on dream recall:
A 30-day diary report. Dreaming, 2, 137–141.
Aspy, D. J., Delfabbro, P., & Proeve, M. (2015). Is dream recall underestimated
by retrospective measures and enhanced by keeping a logbook? A review.
Consciousness and Cognition, 33, 364–374.
Beaulieu-Prevost, D., & Zadra, A. L. (2005). Dream recall frequency and attitude
towards dreams: A reinterpretation of the relation. Personality and Individual
Differences, 38, 919–927.
Belicki, K. (1986). Recalling dreams: An examination of daily variation and indi-
vidual differences. In J. Gackenbach (Ed.), Sleep and dreams: A sourcebook
(pp. 187–206). New York: Garland.
Belicki, K., & Bowers, P. (1982). The role of demand characteristics and hypnotic
ability in dream change following a presleep instruction. Journal of Abnormal
Psychology, 91, 426–432.
DREAM RECALL 29
Dream psychology and the new biology of dreaming (pp. 199–217). Springfield:
Charles C. Thomas.
Eichenlaub, J.-B., Bertrand, O., Morlet, D., & Ruby, P. (2014). Brain reactivity
differentiates subjects with high and low dream recall frequencies during both
sleep and wakefulness. Cerebral Cortex, 24(5), 1206–1215.
Eichenlaub, J.-B., Nicolas, A., Daltrozzo, J., Redoute, J., Costes, N., & Ruby, P.
(2014). Resting brain activity varies with dream recall frequency between sub-
jects. Neuropsychopharmacology, 39(7), 1594–1602.
Fell, J., Fernandez, G., Lutz, M. T., Kockelmann, E., Burr, W., Schaller, C., Elger,
C. E., & Helmstaedter, C. (2006). Rhinal-hippocampal connectivity deter-
mines memory formation during sleep. Brain, 129, 108–114.
Fox, K. C. R., Nijeboer, S., Solomonova, E., Domhoff, G. W., & Christoff, K.
(2013). Dreaming as mind wandering: Evidence from functional neuroimaging
and first-person content reports. Frontiers in Human Neuroscience, 7. https://
[Link]/10.3389/fnhum.2013.00412.
Freud, S. (1900/1991). The interpretation of dreams (Org.: Die Traumdeutung).
London: Penguin Books.
Gedda, L., & Brenci, G. (1979). Sleep and dream characteristics in twins. Acta
Geneticae Medicae et Gemellologiae, 28, 237–239.
Giambra, L. M., Jung, R. E., & Grodsky, A. (1996). Age changes in dream recall
in adulthood. Dreaming, 6, 17–31.
Goodenough, D. R., Shapiro, A., Holden, M., & Steinschriber, L. (1959). A com-
parison of “dreamers” and “nondreamers”. Journal of Abnormal and Social
Psychology, 59, 295–302.
Halliday, G. (1992). Effect of encouragement on dream recall. Dreaming, 2,
39–44.
Hartmann, E. (1991). Boundaries in the mind. New York: Basic Books.
Hill, C. E., Diemer, R. A., & Heaton, K. J. (1997). Dream interpretation sessions:
Who volunteers, who benefits, and what volunteer clients view as most and
least helpful. Journal of Counseling Psychology, 44, 53–62.
Hobson, J. A., & Stickgold, R. (1994). Dreaming: A neurocognitive approach.
Consciousness and Cognition, 3, 1–15.
Hobson, J. A., Pace-Schott, E. F., & Stickgold, R. (2000). Dreaming and the
brain: Toward a cognitive neuroscience of conscious states. Behavioral and
Brain Sciences, 23, 793–842.
Horton, C. L., & Malinowski, J. (2015). Autobiographical memory and hyperas-
sociativity in the dreaming brain: Implications for memory consolidation in
sleep. Frontiers in Psychology, 6. [Link]
Koukkou, M., & Lehmann, D. (1983). Dreaming: The functional state-shift
hypothesis. British Journal of Psychiatry, 142, 221–231.
Koulack, D., & Goodenough, D. R. (1976). Dream recall and dream recall failure:
An arousal-retrieval model. Psychological Bulletin, 83, 975–984.
DREAM RECALL 31
Kramer, M., Roth, T., & Trinder, J. (1975). Dreams and dementia: A laboratory
exploration of dream recall and dream content in chronic brain syndrome
patients. International Journal of Aging and Human Development, 6, 169–178.
Mangiaruga, A., Scarpelli, S., Bartolacci, C., & De Gennaro, L. (2018). Spotlight
on dream recall: The ages of dreams. Nature and Science of Sleep, 10, 1–12.
McCrae, R. R. (1994). Openness to experience: Expanding the boundaries of fac-
tor V. European Journal of Personality, 8, 251–272.
Murri, L., Mancino, M., Massetani, C., Canapicchi, R., Puglioli, M., & Rossi, R.
(1989). Effects of acute and chronic brain damage on dreaming. Research
Communications in Psychology, Psychiatry and Behavior, 14, 121–142.
Myers, W. A., & Solomon, M. (1989). Dream frequency in psychoanalysis and
psychoanalytic psychotherapy. Journal of the American Psychoanalytic
Association, 37, 715–725.
Nielsen, T. A. (2000). A review of mentation in REM and NREM sleep: “Covert”
REM sleep as a possible reconciliation of two opposing models. Behavioral and
Brain Sciences, 23, 851–866.
Nielsen, T. A., Oullet, L., Warnes, H., Cartier, A., Malo, J.-L., & Montplaisir,
J. (1997). Alexithymia and impoverished dream recall in asthmatic patients:
Evidence for self-report measures. Journal of Psychosomatic Research, 42, 53–59.
Pace-Schott, E. F., Gersh, T., Silvestri, R., Stickgold, R., Salzman, C., & Hobson,
J. A. (2001). SSRI treatment suppresses dream recall frequency but increases
subjective dream intensity in normal subjects. Journal of Sleep Research, 10,
129–142.
Parker, J. D. A., Bauermann, T. A., & Smith, C. T. (2000). Alexithymia and
impoverished dream content: Evidence from rapid eye movement sleep awak-
enings. Psychosomatic Medicine, 62, 486–491.
Redfering, D. L., & Keller, J. N. (1974). Influence of differential instruction on
the frequency of dream recall. Journal of Clinical Psychology, 30, 268–271.
Reed, H. (1978). Improved dream recall associated with meditation. Journal of
Clinical Psychology, 39, 150–156.
Riemann, D., Löw, H., Schredl, M., Wiegand, M., Dippel, B., & Berger, M.
(1990). Investigations of morning and laboratory dream recall and content in
depressive patients during baseline conditions and under antidepressive treat-
ment with trimipramine. Psychiatric Journal of the University of Ottawa, 15,
93–99.
Robbins, P. R., & Tanck, R. H. (1988). Interest in dreams and dream recall.
Perceptual and Motor Skills, 66, 291–294.
Schonbar, R. A. (1965). Differential dream recall frequency as a component of
“life-style”. Journal of Consulting Psychology, 29, 468–474.
Schredl, M. (2002). Questionnaire and diaries as research instruments in dream
research: Methodological issues. Dreaming, 12, 17–26.
32 M. SCHREDL
Schredl, M., Jochum, S., & Souguenet, S. (1997). Dream recall, visual memory,
and absorption in imaginings. Personality and Individual Differences, 22,
291–292.
Schredl, M., Bohusch, C., Kahl, J., Mader, A., & Somesan, A. (2000). The use of
dreams in psychotherapy: A survey of psychotherapists in private practice.
Journal of Psychotherapy Practice and Research, 9, 81–87.
Schredl, M., Brenner, C., & Faul, C. (2002). Positive attitude toward dreams:
Reliability and stability of a ten-item scale. North American Journal of Psychology,
4, 343–346.
Schredl, M., Ciric, P., Bishop, A., Gölitz, E., & Buschtöns, D. (2003). Content
analysis of German students’ dreams: Comparison to American findings.
Dreaming, 13, 237–243.
Schredl, M., Landgraf, C., & Zeiler, O. (2003). Nightmare frequency, nightmare
distress and neuroticism. North American Journal of Psychology, 5, 345–350.
Schredl, M., Wittmann, L., Ciric, P., & Götz, S. (2003). Factors of home dream
recall: A structural equation model. Journal of Sleep Research, 12, 133–141.
Schredl, M., Riemann, D., & Berger, M. (2009). The effect of trimipramine on
dream recall and dream emotions in depressive outpatients. Psychiatry Research,
167, 279–286.
Schredl, M., Lahl, O., & Göritz, A. S. (2010). Gender, sex role orientation, and
dream recall frequency. Dreaming, 20, 19–24.
Schredl, M., Kim, E., Labudek, S., Schädler, A., & Göritz, A. S. (2013). Gender,
sex role orientation, and dreaming. Dreaming, 23(4), 277–286.
Schredl, M., Buscher, A., Haaß, C., Scheuermann, M., & Uhrig, K. (2015).
Gender differences in dream socialisation in children and adolescents.
International Journal of Adolescence and Youth, 20, 61–68.
Schredl, M., Stumbrys, T., & Erlacher, D. (2016). Dream recall, nightmare fre-
quency, and spirituality. Dreaming, 26(1), 1–9.
Siclari, F., Baird, B., Perogamvros, L., Bernardi, G., LaRocque, J. J., Riedner, B.,
Boly, M., Postle, B. R., & Tononi, G. (2017). The neural correlates of dream-
ing. Nature Neuroscience, 20(6), 872–878.
Solms, M. (1997). The neuropsychology of dreams: A clinical-anatomical study.
Mahwah: Lawrence Erlbaum.
Spanos, N. P., Stam, H. J., Radtke, H. L., & Nightingale, M. E. (1980). Absorption
in imaginings, sex-role orientation and the recall of dreams by males and
females. Journal of Personality Assessment, 44, 227–282.
Stepansky, R., Holzinger, B., Schmeiser-Rieder, A., Saletu, B., Kunze, M., &
Zeitlhofer, J. (1998). Austrian dream behavior: Results of a representative pop-
ulation survey. Dreaming, 8, 23–30.
Tart, C. T. (1962). Frequency of dream recall and some personality measures.
Journal of Consulting Psychology, 26, 467–470.
34 M. SCHREDL
Taub, J. M. (1970). Dream recall and content following extended sleep. Perceptual
and Motor Skills, 30, 987–990.
Tholey, P., & Utecht, K. (1987). Schöpferisch träumen – Der Klartraum als
Lebenshilfe. Niedernhausen: Falken.
Tribl, G. G., Wetter, T. C., & Schredl, M. (2013). Dreaming under antidepres-
sants: A systematic review on evidence in depressive patients and healthy volun-
teers. Sleep Medicine Reviews, 17, 133–142.
Trotti, L. M. (2017). Waking up is the hardest thing I do all day: Sleep inertia and
sleep drunkenness. Sleep Medicine Reviews, 35, 76–84.
Vallat, R., Chatard, B., Blagrove, M., & Ruby, P. (2017a). Characteristics of the
memory sources of dreams: A new version of the content-matching paradigm
to take mundane and remote memories into account. PLoS One, 12(10),
e0185262.
Vallat, R., Lajnef, T., Eichenlaub, J.-B., Berthomier, C., Jerbi, K., Morlet, D., &
Ruby, P. M. (2017b). Increased evoked potentials to arousing auditory stimuli
during sleep: Implication for the understanding of dream recall. Frontiers in
Human Neuroscience, 11, 132. [Link]
Vallat, R., Meunier, D., Nicolas, A., & Ruby, P. (2017c). Sleep inertia and func-
tional connectivity between brain regions at awakening: An EEG-fMRI study.
International Journal of Dream Research, 10(Suppl 1), S59.
Waterman, D. (1991). Aging and memory for dreams. Perceptual and Motor Skills,
73, 355–365.
Watson, D. (2003). To dream, perchance to remember: Individual differences in
dream recall. Personality and Individual Differences, 34, 1271–1286.
Zadra, A. L., & Robert, G. (2012). Dream recall frequency: Impact of prospective
measures and motivational factors. Consciousness and Cognition, 21, 1695–1702.
Zunker, M., Althoff, H. K., Apel, J., Lässig, H. S., Schültke, L., & Schredl, M.
(2015). Comparing questionnaire and diary measures for eliciting nightmare
frequency. International Journal of Dream Research, 8, 129–134.
CHAPTER 3
3.1 Basics
Dream content analysis is the most important tool in psychological dream
research as this method suffices the common criteria of science such as
possible replication by another research group, assessment of reliability
and validity, and minimizing experimenter bias (Domhoff 1996; Hall and
Van de Castle 1966). The aim of content analysis is to quantify particular
aspects of the verbal material (dream report) in order to carry out statisti-
cal analyses (Schredl 2010). For example, Hall and Van de Castle (1966)
analyzed the nature of aggressive interactions in dreams and found that
50% of the aggressive interactions were of a physical nature in men’s
dreams whereas for women’s dreams the amount was only 34%—a signifi-
cant gender difference. However, the method of content analysis also has
some shortcomings. By applying specific scales, information is lost as only
a few aspects of the dream report can be measured. The uniqueness of a
single dream cannot be captured. A problem which is very important for
interpreting empirical findings is that content analysis relies on dream
reports to measure dream experiences, that is, the question “How close is
the dream report to the original dream experience” is of utmost impor-
tance. If dreamers, for example, do not explicitly report their emotions or
thoughts that occurred in the dream, the content analytic findings are
biased. These issues will be discussed in the validity section.
a diary is the fact that most dream diary studies were carried out in student
samples—even the so-called norms of Hall and Van de Castle (1966) and
not in full-time working persons. Another option for obtaining diary dreams
is to ask for (or the researcher is offered the opportunity by the dreamer)
dream diaries the dreamer kept for personal reasons. G. W. Domhoff (2018)
collected a considerable number of long dream series which are also avail-
able on his website [Link], for example, the Barb Sanders series
encompasses 4254 dreams over a time period of about 26 years. Such a
diary study would not be possible with research participants but it has to be
taken into consideration that only persons with specific characteristics, for
example, interested in personal growth, are willing to put in the effort to
record dreams almost every morning over such a long period in time; sec-
ondly, the dreamer might have selected to record only specific dreams, for
example, those that are puzzling him or her, and mundane dreams are not
recorded. But the opportunity to study how life events affect dreams even
years afterward is compelling, for example, the occurrence of school
friends in dreams 20 years after graduation (Schredl 2012). Interestingly,
Casagrande and Cortini (2008) showed that voice-recording dreams in the
home setting (instead of writing the dream report down) yielded more elab-
orated dream reports that closer the actual dream experience than written
reports. This is an option that should be pursued in the future.
In order to optimize controllability of the experimental situation and
enhance the amount of dream material because of the high recall rates of
about 80% after REM awakenings and 40% after NREM awakenings
(Nielsen 2000) dream reports collected during laboratory awakenings are
considered to be the “gold standard” for obtaining dream material. The
major drawback of this paradigm, however, is the strong effect of the set-
ting on dream content; that is, on average about 20% of the dreams include
direct laboratory references like electrodes, experimenter, and sleep lab
and about 38% direct and indirect references, for example, participating in
an experiment (Schredl 2008b), that is, these dream reports are clearly not
representative of the dream life of the participants in his or her everyday
setting. Furthermore, aggressive and sexual elements occur in laboratory
dreams less often than in home dreams (Domhoff and Kamiya 1964;
Weisz and Foulkes 1970) and also the number of emotions, especially
negative emotions, are reduced in the lab setting (Sikka et al. 2018); find-
ings which are interpreted as an “inhibitory” effect of the lab setting
(including video taping of the sleeper, technical staff presence in the adjacent
room). For investigating sleep physiology in persons with nightmares,
DREAM CONTENT ANALYSIS 39
Formulating a hypothesis
Selecting an existing scale or developing a new one
Eliciting dream reports
Preparing dream reports
Blind rating by external judges
Computing interrater reliability
Statistics
Interpreting the findings
DREAM CONTENT ANALYSIS 41
compute interrater reliabilities because the researcher can refer to the indi-
ces given by the author of the scales or to previous studies using this par-
ticular scale.
It should be very carefully documented how dream reports were elic-
ited (see: Winget and Kramer 1979) since the type of dream report (most
recent dream, diary dream, reports obtained in a sleep lab) might have—as
pointed out above—a strong effect on the findings. As each dream collec-
tion method has pros and cons, it depends on the study’s aims as to which
method is best suited to answer the research question.
After collecting the dream reports, they usually were typed in order to
facilitate blind rating. All information not reflecting the dream experience,
like “I dreamed of my uncle whom I have seen the day before” should be
removed so the judges are not distracted by irrelevant information. For
some research questions, for example, guessing the dreamer’s sex (Schredl
2008a; Schredl et al. 2004), it is necessary to edit the dream more thor-
oughly and remove all explicit references to the dreamer’s sex, for exam-
ple, “My wife has …” changed into “My wife/my husband has …”. The
next step is to bring the dreams into a randomized order, for example,
mixing the men’s dreams and the women’s dreams so the external judge
cannot guess to which group the particular dream belongs (“blind judg-
ing”). Typically the dreams are numbered according to the new order
(viewable for the reviewer) and the researcher keeps a file matching the
new numbers with the group variable (men vs. women) and the original
subject number.
Usually one rater coding all dream reports are sufficient; solely in the
case of scales newly developed for the study, a second rater should rate at
least a subsample (preferably 100 dreams or more) in order to compute
interrater reliability indices. Typical indices are exact agreement, Cohen’s
kappa (e.g., physical aggression present/not present), Spearman Rank
correlations for ordinal scales (e.g., dream bizarreness with four catego-
ries), or Pearson correlations for interval scales (e.g., number of dream
persons).
After coding and entering the coding results in a file, the dream reports
are sorted along the group(s) the dream belongs to in order to perform
statistical tests, for example, a chi-square test whether more men’s dreams
include at least one physical aggression compared to women’s dreams.
The statistics might get more complicated if more than one dream per
participant is included (repeated measurement) or a dream series of one
dreamer is analyzed (see below).
42 M. SCHREDL
a sample of reports from another study (typically 30–50 dream reports are
sufficient for practicing coding). But if not, the question arises how to
develop a new scale. A simple receipt of how to construct a valid dream
content scale seems not to exist. Hall and Van de Castle (1966) suggest
reading a great number of dream reports in order to obtain a picture how
the specific content one is aiming for is appearing in the dream. However, it
is very important not to include the material which should be analyzed since
this will produce a scale that measures exactly those aspects the developer
had put into the scale. The categories should be formulated as exact and
comprehensive as possible. The aim from a methodological viewpoint is to
obtain a high interrater agreement if two or more judges apply the same
scale to the same dream sample, that is, the more detailed the coding rules
are formulated the simpler are the decisions for the external judge. However,
one has to keep in mind that there are always “grey areas” and special cases
which cannot be grasped by the categories of a scale (Domhoff 1996). An
example is presented in Table 3.2. Whereas this specific scale measures the
number of persons in the dream comparable to a waking-life experience or
theater play, Hall and Van de Castle (1966) have chosen a broader defini-
tion: they include persons who are mentioned in a conversation or if objects
which belong to a specific person occur within the dream. This example
illustrates that even simple parameters like the number of dream persons
depend on the coding rules which should be as explicit as possible. This
example also illustrates the arbitrariness of the scale’s definition, for exam-
ple, one might argue whether counting groups as one person makes sense.
How many single persons occur in the dream? For example, father, child, friend, and so
on or unknown persons
Groups which are mentioned solely as group will be coded as single person, even if
the description include the group size, for example, eight persons. If members of the
group appear in the course of the dream as single persons, they were coded separately.
Similarly, a division into subgroups will be counted for each new subgroup
If a person underwent a metamorphosis, that is, an identity change is taking place, this
will be coded as one single person
Each person who appears in the dream will only be coded once
If persons seeking contact to persons or objects which belong to other persons (e. g. the
car of my uncle) are only mentioned in the dream, these references were not coded
The dreamer herself/himself will not be coded
44 M. SCHREDL
In this case this option was chosen to avoid totally screwed data distribution,
for example, “I saw a group of about hundred people” would yield a very
high value. As the external ratings depend on the definition of the catego-
ries, the findings of a dream content analytic study should be particularly
careful evaluated with respect to these specific scales’ definitions.
After developing the first draft of the scale, two or more judges should
rate independently a number of dream reports in order to compute inter-
rater reliability coefficients. If the coefficients are low, the researcher
should discuss the disagreements regarding the coding between the judges
with the judges and revise the scale according to this new information. In
order to determine whether the interrater reliability improved, one has to
keep in mind to select new judges for the same material or select another
sample of dreams for the coding. Specific guidelines or cut-off values
about what classifies as “good” and “poor” reliability coefficients do not
exist in the dream research literature.
Content analytic scales in the narrow sense are defined as nominal scale,
for example, occurrence of persons (mother, child, friend, etc.) or aggres-
sive interaction (physical, verbal, etc.) within the dream; the rating system
of Hall and Van de Castle (1966) is using this type of scales. After the
dream(s) are coded, sum indices can be obtained, for example, number of
dream characters, number of aggressive interactions, and so on.
Furthermore, Hall and Van de Castle (1966) differentiated between
empirical and theoretical scales. Empirical scales were derived by reading
through many dream reports to look for topics which occur often in
dreams or have been of special interest to them. The above-mentioned
scale for measuring the number of dream persons is an example for an
empirical scale. The fact that this scale is also not free from making assump-
tions becomes obvious if one compares the coding of persons who appear
in the dream versus coding persons who were only mentioned in the
dream. Hall and Van de Castle (1966) have derived theoretical scales from
the psychoanalytic theory by making a variety of prepositions: the scales
“penis envy”, “castration anxiety” and “castration wish”. Looking at the
coding rules and the examples of the castration anxiety scale, for example,
“My finger was cut off”, “I wasn’t able to get an erection”, “I couldn’t get
my key in the lock” illustrates the fact that a lot of assumptions went into
the construction of that scale (e.g., metaphorical analogies); the correct-
ness of these assumptions can be debated (Domhoff 1996). The finding
that men tend to more often have dreams including penis envy (N = 25)
DREAM CONTENT ANALYSIS 45
In four steps the closeness of the dream action to everyday reality should be estimated.
Are the dream events part of everyday life of a person of a Western culture or are they
uncommon or impossible?
(1) Possible in waking life and dream events are part of the normal everyday life
(2) Many elements of the waking life, but the dream action is uncommon and
impossible for the dreamer in real life
(3) Occurrence of one or two fantasy objects, bizarre connections, or actions that are
not possible in the real world
(4) Occurrence of several fantasy objects, bizarre connections, or actions that are not
possible in the real world
46 M. SCHREDL
a factor analysis of 20 ordinal scales and obtained six factors: “vivid fan-
tasy” (including realism/bizarreness), “active control”, “pleasantness”,
“verbal aggression”, “physical aggression” and “heterosexuality”. Based
on these findings and own experiences, the manual of Schredl (1991) and
the subsequent versions (Schredl 1998b; Schredl et al. 1996, 1998, 1999)
enclosed the basic scales which are depicted in Table 3.5.
The advantage of this rating system is the simple applicability of the
basic scales; it is much less time-consuming than coding dreams according
to the rating system of Hall and Van de Castle (1966). In addition, as
pointed out above, it does make sense to add only scales that are specifi-
cally aiming at the study’s hypotheses; even if they have to be newly devel-
oped for the study. For example, Schredl (1991) developed a three-point
scale for measuring the occurrence of problems within a dream (none,
minor, and major problems) in order to test the hypothesis whether
patients with insomnia tend to have more problematic dreams than healthy
controls. Another example was provided by Schredl and Montasser (1999)
who investigated the dreams of anorectic and bulimic patients; they con-
structed scales measuring the occurrence of food themes and food rejec-
tion in dreams. The global rating scales allow the assessment of emotional
intensity of the dream and can be easily applied to short dream reports.
The manual of Hall and Van de Castle (1966) recommends using the
system for dream reports with 50–300 words. The interrater reliability
coefficients are mostly sufficient (see next section). The experiences of the
various studies applying the system, for example, dreaming in the elderly
(Schredl, Schröder, et al. 1996), dreaming and eating disorders (Schredl
and Montasser 1999), gender differences in dreams (Schredl et al. 1998),
sion revealed that one judge who grew up in another culture (Egypt) rated
the realism of dream events in a different way as the other judge who grew
up in Germany. The interrater agreement of the general nominal scales,
for example, aggression, verbal interaction, was satisfactory with values
ranging from 88% to 100% (Schredl et al. 1998).
One might speculate that training and experience with coding dreams
might increase interrater reliability. So far only one systematic study on
this topic has been carried out (Schredl, Burchert, and Grabatin 2004). In
this study two raters first coded the same 100 dreams, then they discussed
their discrepancies and coded another 100 dreams. Again the discrepan-
cies were discussed and the third set of 100 dreams was coded. For the
verbal interaction scale the exact agreement went up significantly from
87% to 95%, whereas for other scales like bizarreness, positive and negative
emotions, and number of dream persons the training did not increase the
reliability which was quite high in the beginning ranging from r = 0.642
to r = 0.926 (Schredl et al. 2004). More studies on the effect of training
the judges on the reliability of the scales are desirable.
As mentioned above, the problem of validity is more complicated as
validity means the extent to which the scale’s measurement value is related
to the dimension which one would like to measure. Many rating systems
(e.g., Hall and Van de Castle 1966) rely on the so-called face validity: if the
external judge looks for explicitly mentioned emotions such as guilt, anxi-
ety, fear, embarrassment as explications of “apprehension” scale, the scale
measures the occurrence of apprehension in the dream. This seems very
straightforward, you get what you see. However, this coding of explicitly
mentioned emotions has its shortcomings as the ultimate goal is not to
measure whether the dreamer explicitly mentioned an emotion that can be
classified as apprehension within the dream report but the question whether
the dreamer experienced the emotion while dreaming. The following fic-
tive dream report will illustrate this line of thinking: “I see a monster and
run away as fast as I can.” It can be hypothesized that the dream ego expe-
riences fear but did not mention it explicitly in her or his dream report. The
emotion score of zero—if only explicitly mentioned emotions are scored—
did not reflect the emotion which was present while dreaming. So the
validity problem is not due to badly constructed scales but arises mainly
because the analyzed dream reports are more or less detailed in reflecting
the actual dream experience. One possible approach to this issue is to com-
pare self-ratings of the dreamer obtained after she/he recorded the dreams.
The basic assumption is that the dream experience is “fresh”, that is, the
52 M. SCHREDL
dreamer has still direct access to the dream emotions she/he experienced
in the dream. For example, the total score of aggression (Gottschalk-Gleser
rating system) correlated with the global estimate of aggression made by
the dreamer to r = 0.53 (Stegie 1986). Using similar four-point scales for
measuring dream emotions, the correlations between external ratings and
self-ratings of the dreamer were satisfactory: negative emotions: r = 0.669
and positive emotions: r = 0.557 (Schredl and Doll 1998). Validity coeffi-
cients of r = 0.53 or r = 0.67 can be viewed as good since the scale’s exter-
nal validity coefficient cannot exceed its reliability coefficient.
For measuring dream emotions, validity issues will be illustrated. One
problem of earlier studies (Hauri et al. 1967) was that they used a bipolar
scale for measuring emotional tone (strongly negative to strongly positive)
because Gaillard and Phelippeau (1977) have shown that 13% of all dreams
included positive and negative emotions. In a sample of diary dreams, the
proportion (34%) of dreams including positive and negative emotions was
still higher (Schredl and Doll 1998). Even if the external judge subtracts
the positive and negative emotions, it seems quite obvious that a dream
with intense negative and positive emotions is different from a neutral
dream, that is, it seems better (more valid) to use two scales for measuring
positive and negative emotions separately. Another problem was the ques-
tion whether the dreamer experiences the same emotions in specific dream
situations which she/he also would experience if he faced the same situa-
tion in waking life, for example, seeing a horrible monster induces fear
(appropriateness of dream emotions). Foulkes, Sullivan, Kerr, and Brown
(1988) and Merritt, Stickgold, Pace-Schott, Williams, and Hobson (1994),
however, have shown that such validity errors due to inappropriateness of
the dream emotion occurred in less than 5% of the dreams, that is, the
experiencing within the dream is very similar to experiencing in waking life.
Schredl and Doll (1998) have investigated the relationship between three
types of scales, the emotion scales of Hall and Van de Castle, the two emo-
tion rating scales for external judges constructed by Schredl (1991), and
two self-rating scales for measuring positive and negative dream emotions.
Almost 60% of the 133 dream reports included no explicitly mentioned
emotion (Hall and Van de Castle rating system) whereas the self-ratings of
the dreamer indicated that only 0.8% of the dreams did not include a posi-
tive and/or negative emotion, that is, the findings of this study clearly
demonstrate an underestimation of dream emotions if the Hall and Van de
Castle emotion scales are applied (Schredl and Doll 1998). In addition, the
rating scales designed for judges with the similar format of the self-rating
scales (four-point: none, mild, moderate, strong) did show a marked
DREAM CONTENT ANALYSIS 53
Table 3.6 Checklist for interpreting the findings of a dream content analytic
study
Issue
Sample characteristics
Number of dream reports per participant
Type of dream report
Reliability of the content analytic scales
Validity of the content analytic scales
Appropriate statistical procedure applied
ticipant younger than 25 years (60.3% men’s dreams vs. 46.6% women’s
dream), that is, showing the “ubiquitous” gender difference, but in the
total sample (mean age of about 34 years ranging from 14 to 86 years) the
ratios were different: 59.2% of the dream characters in women’s dreams
were male and only 42.4% in the men’s dreams (Schredl et al. 2010–2011),
reversed compared to the figures obtained in student samples clearly indi-
cating that findings based on student samples cannot be generalized. The
notion of “norms” assigned to the first big dream collection of 500 dreams
of 100 female students and 500 dreams of 100 male students (Hall and
Van de Castle 1966) should be viewed with caution. Similar consider-
ations of the representativeness of samples apply also to clinical samples,
for example, are the participants self-selected (regarding their interest in
dreams) and participated because it is a dream study. In studying dream
content, there is an additional challenged to be faced. Winget, Kramer,
and Whitman (1972) selected 300 persons roughly representative of the
city of Cincinnati, of those 300 participants only 182 (about 61%) reported
a dream. In another representative study (Schredl and Keller 2008–2009)
only 36.8% of the interviewed persons reported a dream; the not report-
ing a dream was associated with dream recall frequency and older age.
That means that the original sample was representative, but the sample of
dream reporters were not; this should be kept in mind as dream recall is
related to a number of personality variables, for example, openness to
experience (Schredl and Göritz 2017) and other variables (see Chap. 2).
For correlating dream content with trait factors, for example, personality
dimension, it is necessary to measure inter-individual differences in dream
content reliably. Kramer and Roth (1979) addressed the stability respec-
tively the variability of dream content empirically in 14 participants who
were awakened out of REM sleep over 20 consecutive nights. Their find-
ings showed that the sum scores (number of dream persons, physical activi-
ties, verbal activities) based on three to five REM dreams per night correlated
DREAM CONTENT ANALYSIS 57
As pointed out in the Sect. 3.2, it is important to take into account the
type of dream reports that have been analyzed, most recent dreams, diary
dreams, or laboratory dreams. Each of these dream types has its pro and
cons, for example, if the researcher is interested in dream emotions, one
might get biased results if only laboratory dreams were collected. The
issues of reliability and validity are also of importance for interpreting the
findings, especially the validity aspect. As mentioned above, dream con-
tent analysis done by external judges might underestimate the occurrence
of dream emotions, that is, for this topic self-rating scales completed by
the dreamer are more appropriate.
Lastly, using the adequate statistics is important for interpreting signifi-
cant results; the most common mistake is to inflate the degrees of freedom
by using the dream report as unit although participants contributed sev-
eral reports—a recent example is the study of Voss et al. (2014). The appli-
cation of more complex statistical procedures in dream research is
increasing.
To summarize, despite the various issues that have to be considered, the
dream content analysis method is a straightforward method that can be
used also by novices—if applied and interpreted properly. Several topics
like validity of dream content analytic scales or applying the appropriate
statistical procedures to the data set have to be studied more thoroughly
in the future.
References
Bandalos, D. L. (2018). Measurement theory and applications for the social sciences.
New York: Guilford Publications.
Beck, A. T., & Hurvich, M. S. (1959). Psychological correlates of depression:
I. Frequency of “masochistic” dream content in a private practice sample.
Psychosomatic Medicine, 1, 50–55.
Bernstein, D. M., & Belicki, K. (1995). On the psychometric properties of retro-
spective dream content questionnaires. Imagination, Cognition and Personality,
15, 351–364.
Brink, S. M., & Allan, J. A. B. (1992). Dreams of anorexic and bulimic women: a
research study. Journal of Analytical Psychology, 37, 275–297.
Bulkeley, K. (2009). Seeking patterns in dream content: A systematic approach to
word searches. Consciousness and Cognition, 18, 905–916.
Bulkeley, K. (2014). Digital dream analysis: A revised method. Consciousness and
Cognition, 29, 159–170.
DREAM CONTENT ANALYSIS 59
Cartwright, R. D., & Kaszniak, A. (1991). The social psychology of dream report-
ing. In S. J. Ellman & J. S. Antrobus (Eds.), The mind in sleep: Psychology and
psychophysiology (pp. 251–264). New York: Wiley.
Casagrande, M., & Cortini, P. (2008). Spoken and written dream communication:
Differences and methodological aspects. Consciousness and Cognition, 17(1),
145–158. [Link]
Cipolli, C., Bolzani, R., Cornoldi, C., De Beni, R., & Fagioli, I. (1993). Bizarreness
effect in dream recall. Sleep, 16, 163–170.
Clark, J., Trinder, J., Kramer, M., Roth, T., & Day, N. (1972). An approach to the
content analysis of dream content analysis scales. Sleep Research, 1, 118.
Cohen, J. (1960). A coefficient of agreement for nominal scales. Educational and
Psychological Measurement, 20, 37–46.
Dippel, B. (1988). Manual zur Erfassung des manifesten Trauminhaltes ([Link],
204 Items). München: Unveröffentlichtes Manuskript.
Domhoff, G. W. (1996). Finding meaning in dreams: A quantitative approach.
New York: Plenum Press.
Domhoff, G. W. (2018). The emergence of dreaming: Mind-wandering, embodied
simulation, and the default network. New York: Oxford University Press.
Domhoff, B., & Kamiya, J. (1964). Problems in dream content study with objec-
tive indicators: I. A comparison of home and laboratory dream reports. Archives
of General Psychiatry, 11, 519–524.
Enke, H., Ohlmeier, D., & Nast, J. (1968). Eine formale Affekt- und
Beziehungsanalyse in Traumserien von Patienten mit psychosomatischen
Krankheitsbildern. Zeitschrift für Psychosomatische Medizin, 9, 15–33.
Foulkes, D. (1978). A grammar of dreams. New York: Harvester Press.
Foulkes, D. (1982). Children’s dreams: Longitudinal studies. New York: Wiley.
Foulkes, D., & Sheperd, J. (1971). Manual for a scoring system for children’s
dreams. Unpublished manuscript, University of Wyoming.
Foulkes, D., Sullivan, B., Kerr, N. H., & Brown, L. (1988). Appropriateness of
dream feelings to dreamed situations. Cognition and Emotion, 2, 29–39.
Gaillard, J.-M., & Phelippeau, M. (1977). Analysis of dream contents by scaled
and rated measurements. Psychological Medicine, 7, 275–282.
Germain, A., Hall, M., Shear, M. K., Nofzinger, E. A., & Buysse, D. J. (2006).
Sleep disruption in PTSD: A pilot study with home-based polysomnography.
Sleep and Biological Rhythms, 4, 286–289.
Gottschalk, L. A., Gleser, G., & Springer, K. J. (1963). Three hostility scales appli-
cable to verbal samples. Archives of General Psychiatry, 9, 254–279.
Hall, C. S. (1984). “A ubiquitous sex difference in dreams” revisited. Journal of
Personality and Social Psychology, 46, 1109–1117.
Hall, C. S., & Domhoff, B. J. (1963). A ubiquitous sex difference in dreams.
Journal of Abnormal and Social Psychology, 66, 278–280.
60 M. SCHREDL
Hall, C. S., & Van de Castle, R. L. (1966). The content analysis of dreams.
New York: Appleton-Century-Crofts.
Hauri, P. (1975). Categorization of sleep mental activity for psychophysiological
studies. In G. C. Lairy & P. Salzorulo (Eds.), The experimental study of human
sleep: Methodological problems (pp. 271–281). Amsterdam: Elsvier.
Hauri, P., Sawyer, J., & Rechtschaffen, A. (1967). Dimensions of dreaming: A
functional scale for rating dream reports. Journal of Abnormal Psychology, 72,
16–22.
Heather-Greener, G. Q., Comstock, D., & Joyce, R. (1996). An investigation of
the manifest content associated with migraine headaches: A study of dreams
that precede nocturnal migraines. Psychotherapy and Psychosomatics, 65,
216–221.
Hopf, H. H. (1989). Wie “objektiv” sind unsere Notizen? Ein Vergleich von
Patiententraumprotokollen mit von Therapeuten niedergeschriebenen
Protokollen. Kind und Umwelt, 63, 42–52.
Kemp, S., Burt, C. D. B., & Sheen, M. (2003). Remembering dreamt and actual
experiences. Applied Cognitive Psychology, 17, 577–591.
Klingenberg, B. (2008). Regression models for binary time series with gaps.
Computational Statistics and Data Analysis, 52(8), 4076–4090.
Kramer, M. (2010). The assessment of dream content: Methodological consider-
ations. Sleep Medicine Clinics, 5(2), 183–191.
Kramer, M., & Roth, T. (1979). The stability and variability of dreaming. Sleep, 1,
319–325.
Leuschner, W., Hau, S., Brech, E., & Volk, S. (1994). Disassociation and reasso-
ciation of subliminally induced stimulus material in drawings of dreams and
drawings of waking free imagery. Dreaming, 4, 1–27.
Lloyd, S., & Cartwright, R. D. (1995). The collection of home and laboratory
dreams by means of an instrumental response technique. Dreaming, 5, 63–73.
Merritt, J. M., Stickgold, R., Pace-Schott, E., Williams, J., & Hobson, J. A.
(1994). Emotion profiles in the dreams of men and women. Consciousness and
Cognition, 3, 46–60.
Nielsen, T. A. (2000). A review of mentation in REM and NREM sleep: “Covert”
REM sleep as a possible reconciliation of two opposing models. Behavioral and
Brain Sciences, 23, 851–866.
Okuma, T., Fukuma, E., & Kobayashi, K. (1975). “Dream detector” and com-
parison of laboratory and home dreams collected by REMP-awakening tech-
nique. In E. D. Weitzman (Ed.), Advances in sleep research (Vol. 2, pp. 223–231).
New York: Spectrum Publications.
Paul, F., Schredl, M., & Alpers, G. W. (2015). Nightmares affect the experience of
sleep quality but not sleep architecture: An ambulatory polysomnographic
study. Borderline Personality Disorder and Emotion Dysregulation, 2(3), 1–9.
Rost, J. (1996). Lehrbuch Testtheorie. Bern: Huber.
DREAM CONTENT ANALYSIS 61
Schredl, M., Fuchedzhieva, A., Hämig, H., & Schindele, V. (2008). Do we think
dreams are in black and white due to memory problems? Dreaming, 18,
175–180.
Schredl, M., Desch, S., Röming, F., & Spachmann, A. (2009). Erotic dreams and
their relationship to waking-life sexuality. Sexologies, 18, 38–43.
Schredl, M., Paul, F., Lahl, O., & Göritz, A. S. (2010–2011). Gender differences
in dream content: Related to biological sex or sex role orientation? Imagination,
Cognition, and Personality, 30, 171–183.
Sikka, P., Feilhauer, D., Valli, K., & Revonsuo, A. (2017). How you measure is
what you get: Differences in self- and external ratings of emotional experiences
in home dreams. American Journal of Psychology, 130(3), 367–384.
Sikka, P., Revonsuo, A., Sandman, N., Tuominen, J., & Valli, K. (2018). Dream
emotions: A comparison of home dream reports with laboratory early and late
REM dream reports. Journal of Sleep Research, 27, 206–214.
Stegie, R. (1986). Zur Anwendung des Gottschalk-Gleser-Verfahrens in einer psy-
chophysiologischen Traumstudie. In U. Koch & G. Schoefer (Eds.),
Sprachinhaltsanalyse in der psychiatrischen und psychosomatischen Forschung
(pp. 424–437). Weinheim: Psychologie Verlags Union.
Stern, D. A., Saayman, G. S., & Touyz, S. W. (1978). A methodological study of
the effect of experimentally induced demand characteristics in research of noc-
turnal dreams. Journal of Abnormal Psychology, 87, 459–462.
Strauch, I., & Meier, B. (1996). In search of dreams: Results of experimental dream
research. Albany: State University of New York Press.
Trinder, J., Kramer, M., Riechers, M., Fishbein, H., & Roth, T. (1970). The effect
of dream length on dream content. Psychophysiology, 7, 333.
Urbina, S. P. (1981). Methodological issues in the quantitative analysis of dream
content. Journal of Personality Assessment, 45, 71–78.
Voss, U., Holzmann, R., Hobson, A., Paulus, W., Koppehele-Gossel, J., Klimke,
A., & Nitsche, M. A. (2014). Induction of self awareness in dreams through
frontal low current stimulation of gamma activity. Nature Neuroscience, 17(6),
810–812.
Weisz, R., & Foulkes, D. (1970). Home and laboratory dreams collected under
uniform sampling conditions. Psychophysiology, 6, 588–596.
Whitman, R. M., Kramer, M., & Baldridge, B. J. (1963). Which dream does the
patient tell? Archives of General Psychiatry, 8, 277–282.
Winget, C., & Kramer, M. (1979). Dimensions of dreams. Gainesville: University
of Florida Press.
Winget, C., Kramer, M., & Whitman, R. M. (1972). Dreams and demography.
Canadian Psychiatric Association Journal, 17, 203–208.
CHAPTER 4
toward dreams and the Big Five personality factor “openness to experience”
(Schredl 2011b). The finding that the benefit of reading books about
dreams is varying considerably (Schredl 2011b) is an interesting topic for
future research. Anecdotes about dream stimulating waking-life creativity
have been reported fairly often, for example, August Kekulé discovering the
ring structure of benzene (Barrett 2001). Schredl and Erlacher (2007) were
able to demonstrate that dream effects on creativity are not a privilege of
geniuses but also occur in about 8% in the dreams of “normal” people. The
most frequent effect of dreams is the carry-over effect of the dream mood
into waking life (Schredl 2000b), especially negatively toned dreams
(Schredl 2009a) and nightmares (Köthe and Pietrowsky 2001) can exhibit
a strong effect on daytime mood. Interestingly, dreams that are effected by
daytime experiences are more likely to affect the mood of the next day, indi-
cating that relevant and stressful experiences are processed by the mind day
and night (Schredl and Reinhard 2009–2010).
Over the years, questionnaires addressing dream-related behavior,
dream themes, general dream characteristics (like colors and sounds), and
specific dream elements (like aggression and friendliness) have been devel-
oped: the multidimensional dream inventory (Kallmeyer and Chang
1997), Dream Content Questionnaire (DCQ) (Bernstein et al. 1995),
Dream Content Questionnaire for Children (ChDCQ) (Bruni et al.
1999), Dream style questionnaire (Gruber 1988), the Van Dream Anxiety
Scale (VDAS) (Agargün et al. 1999), the KJP dream inventory (Kroth
et al. 1999), the Dream Property Scale (Takeuchi et al. 2001), Dream
motif scale (Yu 2012), and the Düsseldorf Dream Inventory (DDI)
(Aumann et al. 2012). Although most of these questionnaires showed
adequate reliability, for example, measured as internal consistency of com-
posite scores derived from factor analyses or in terms of retest reliability,
the question as to how valid these questionnaire measures of dream con-
tent are is still an open question, as especially in low dream recallers the
dream content analytic results do not match the questionnaire findings
(Schredl 2002). Bernstein and Belicki (1995) and Schredl (2002) pro-
vided data showing the correlations between questionnaire measures of
dream content and measures derived from dream content analysis of
dream reports are very low, especially for low dream recallers. Within this
area, more research is needed to evaluate the psychometric quality of ques-
tionnaires aimed at eliciting dream content. Another interesting approach
to measure specific aspects of dream content is the use of items that are
aiming at a percentage of a specific dream topic in relation to all remem-
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 67
bered dreams, for example, sports dreams, dreams about music, and so on.
It could be demonstrated that frequencies of sport dreams obtained by
this type of questionnaire measure matched the findings of a diary study;
both studies (Erlacher and Schredl 2004; Schredl and Erlacher 2008)
compared dreaming in psychology and sport students.
A recently developed questionnaire (MADRE) elicited in a comprehen-
sive manner the most relevant dream-related variables including dream
recall frequency, nightmare frequency, interest in dreams, creative effects,
dream sharing frequency, and so on (Schredl et al. 2014). This question-
naire showed for most items a sufficient retest reliability and is freely avail-
able in German and English (appendix to the publication).
are unusual for the dreamer, for example, talking to the German chancel-
lor in one of our dream studies. Although about 30% of diary dreams
include at least one element which is not possible in waking life (Schredl
et al. 1999), one has to keep in mind that dream content analytic studies
are likely to underestimate bizarre elements, mostly those not in the focal
point of the dream action (Schredl and Erlacher 2003), that is, the per-
centage of bizarre dreams might be higher.
However, if the criteria for bizarreness are defined in a broader way
(Hobson et al. 1987), for example, abrupt scene changes, or something
like being in the hometown where there is a building that is not there in
reality, up to 75% of the laboratory dreams include this kind of bizarre ele-
ments (Strauch and Meier 1996), that is, different definitions of bizarre-
ness yield different results.
Regarding dream emotions, Hall and Van de Castle (1966) obtained
only 20% positive emotions and 80% negative emotions. As pointed out in
Sect. 3.6, the validity of external ratings of dream emotions based solely
on the dream report is questionable. In Table 4.2 two studies using ratings
made by the dreamer are depicted showing that positive and negative
dreams are almost balanced. In contrast, the external ratings of the same
1207 dream reports yielded a 3:1 ratio of negative to positive dreams—
clearly supporting the aforementioned problems with measuring dream
emotions.
In their sample of 552 diary dreams, Sikka et al. (2017) found even
more positive dreams (55.8%) compared to 35.3% negative dreams by ana-
lyzing the self-ratings of the dreamers; the external ratings of the same
Table 4.2 Dream emotions (global self-ratings and external judge-based ratings)
Category Laboratory Diary dreams b Diary dreams b
dreams a (%) (Self-ratings) (%) (external raters) (%)
(N = 500) (N = 1207) (N = 1207)
Snyder (1970)
a
b
McCarley and Hoffman (1981)
Zadra et al. (1997)
c
70 M. SCHREDL
ture sensations of the dreamer and about 1.0% of the dreams included pain
(Schredl 2016). Pain dreams were more prominent in patients with
chronic back pain (Schredl et al. 2017) but the percentage of 16% pain
dreams indicate that even if pain is very frequent in waking life it rarely
shows up in dreams. Due to the limitations of dream content analysis, the
percentages of “rare” sensory perceptions should be viewed with caution;
whereas visual and auditory perception, for example, talking to someone
is often mentioned explicitly in the dream report, the subtler perceptions
are not; more studies using self-ratings of the dreamer are needed.
As dreams are dominated by visual perceptions, very early the question
arose whether and how congenitally blind persons dream; Heermann
(1838) reported that these persons can remember dreams but without
visual images. In his data, persons who got blind after the age of seven
years still had visual images years later. Although visual impressions are
lacking completely, the number of dream persons, social interactions, and
so on are quite similar to dreams of seeing individuals (Kerr et al. 1982).
Often the dream reports cannot be differentiated at first sight, that is,
whether the dream report stems from a blind or seeing person since blind
persons can describe settings in a detailed way, spatial relations without
having explicit visual perception—even words like seeing are used (Kerr
and Domhoff 2004). These findings indicate that dreams are not visual
images played in the mind but actual experiences very similar to waking-
life experiences (see Chap. 1).
Normally very few color impressions were explicitly reported in dreams,
about 25% (Kahn et al. 1962). However, if the participants are asked
directly upon awakening to name the colors of all major dream objects,
the percentage increased up to almost 100% (Rechtschaffen and Buchignani
1992; Schredl et al. 2008). These findings again indicate that dream con-
tent analysis relying on the dreamer’s skills to report everything she/he
experiences in the dream might have its shortcomings in several areas.
Interestingly, during the era of black-and-white mass media a considerable
percentage of persons thought their dreams were also black-and-white
(Schwitzgebel 2002). A more recent study (König et al. 2017) showed
that in our days most people think their dreams are in color—as the media
switched from black-and-white to color; a very small number (0.53%) of
the generation only exposed to color media think that all their dreams are
black-and-white. The simplest explanation of these changes is that most
persons do not recall the colors of the dreams—except they play a domi-
nant role in the dream, for example, a blue elephant—and adding the
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 71
common analogy between films and dreams the people only thought their
dreams were black-and-white. If, for example, the faces of all dream char-
acters would be gray, the dreamer might notice and remember this strange-
ness. In sum, dreams are—according to the continuity hypothesis of
dreaming (see Sect. 4.3)—as colorful as waking life, but it seems not quite
simple to remember normal colors like yellow bananas or skin colors.
Another topic that has received little attention is the occurrence of cog-
nitive activities (thinking) as this is not mentioned by many dreamers in
their dream reports. Meier (1993), for example, has demonstrated that
cognitive activities (thinking) occur in 21.2% of laboratory dreams.
Carefully conducted studies in trained participants yielded higher percent-
ages of cognitive activities (Kahan and Claudatos 2016).
These facts and many others obtained from the content analysis of many
dream series have led us to formulate what we call the continuity hypothesis.
This hypothesis states that dreams are continuous with waking life; the
world of dreaming and the world of waking are one. The dream world is
neither discontinuous nor inverse in its relationship to the conscious world.
We remain the same person, the same personality with the same characteris-
tics, and the same basic beliefs and convictions whether awake or asleep. The
wishes and fears that determine our actions and thoughts in everyday life
also determine what we will dream about p. 104.
72 M. SCHREDL
How can we reconcile the continuity hypothesis with the obvious fact that a
person will do something in his dreams that he would not or could not do in
a waking state? He will, for example, torture someone to death, have sex with
his young daughter, betray his best friend, or fly through the air. The answer
to this dilemma is to be found in the distinction between overt behavior
(‘acting out’) and covert behavior (thoughts, feelings, and fantasies). The
continuity may be between dreams and covert behavior or it may be between
dreams and overt behavior. A person who has many sex or aggression dreams
may either have many fantasies of sex or aggression when he is awake, or he
may have many actual sexual or aggressive experiences. In either case he is
preoccupied with sex or aggression, awake or asleep. Although when asleep
these preoccupations have fewer limitations, allowing the dreamer to experi-
ence tremendous diversity in his sexual and aggressive fantasies p. 104.
put these elements together into a story (Hobson 1988), that is, dream
content is related to waking life.
For empirical researchers studying the continuity hypothesis the ques-
tion arises whether there are factors that affect the probability of a specific
waking-life experience, preoccupation, or thought to be incorporated into
a subsequent dream. After an overview of paradigms used to study conti-
nuity between waking and dreaming some of those factors that might
affect the continuity are reviewed, for example, time interval between
waking-life experience and dream, emotional intensity of the waking-life
experience, type of the waking-life experience.
Table 4.4 Paradigms for studying the relationship between waking and
dreaming
Research paradigms
REM awakenings) with their waking life. The ability of the dreamers to
relate dream elements to waking life varied considerably: 30.9% of the
dream objects had been seen in waking life and 76.3% key dream charac-
ters were known to the dreamers. For 80 key dream characters, for exam-
ple, the time distribution (including meeting/talking to the person but
also thinking about the person) was as follows: 67.6% pervious day, 19.7%
previous week, 7.0% previous year, 5.6% more than one year ago. Vallat,
Chatard, Blagrove, and Ruby (2017) carried out a field study providing a
questionnaire with questions about the occurrence of the dream element
in waking life. For example, the intensity of the dream element within the
dream was lower compared to the intensity of the corresponding waking-
life experience. Furthermore, waking-life experiences dating back a longer
time interval were rated to be more important and emotionally more
intense than waking-life experience of the previous day (Vallat et al. 2017).
Even though this method seems straightforward, there are at least three
problematic issues: (1) Memory. If waking thoughts are included in addi-
tion to waking-life events, it might be very difficult to recall all the thoughts
of the previous day, let alone of the previous week and therefore an expo-
nential decrease of the incorporation rate with time might just reflect the
ability of the participants to remember the connections, (2) Multiple cor-
respondences. If the person dreams about his mother this might corre-
spond with a telephone conversation two days ago or is related to a
childhood experience. (3) Closeness of correspondences. It should be kept
in mind that dreaming only very rarely includes exact replays of episodic
memories of waking-life experiences (Fosse et al. 2003; Malinowski and
Horton 2014b), that is, there is always some transformation. In the study
of Vallat, Chatard, et al. (2017) participants had to tell whether they felt
that parts of their dream were obviously related to some features of their
waking lives, whereas Blagrove, Henley-Einion, Barnett, Edwards, and
Seage (2011) constructed a scale with a different level of matching between
the contents of the dream report and the waking-day events recorded in
the diary: 0 = no matches at all between dreams and events, 1 = general
matches but these may be recurring themes, 2 = some vague resonances, it
is possible that dream and day are related, 3 = weak relationships between
dreams and events, 4 = several matches or one strong match, and 5 = mul-
tiple strong matches between dreams and events. The participants should
match a diary record of one day and a dream report. It seems obvious that
matching might be done very differently due to the instruction but also
between persons. Due to these problems, the findings obtained by this
retrospective approach are limited in their interpretation regarding the
continuity between waking and dreaming.
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 75
problem, the probability of dreaming about this problem was higher com-
pared to a control condition without incubation: an increase from 20% to
40% of the dreams that were related to the personal problem (Strauch and
Meier 1996). As field studies (e.g., Breger et al. 1971) showed much
stronger effects for “real” stressors, one might speculate that watching a
film in the lab does not have a high personal significance and thus the film
contents are not incorporated into dreams. In order to increase the per-
sonal involvement of the participants, Wegner et al. (2004) instructed his
participants not to think about the target person (a person of the dream-
er’s life) which is a quite demanding task and obtained more occurrences
of the target in subsequent dreams than after just thinking about the per-
son; supporting the ironic-process theory. Subsequent studies (Bryant
et al. 2011; Kröner-Borowik et al. 2013; Taylor and Bryant 2007) using
idiosyncratic intrusive thoughts as targets that should be suppressed (not
thought about) replicated the findings of the first study. In a sleep lab
study (Schmidt and Gendolla 2008), the same effect was found for sleep
onset dreams, this time using an image of three white bears and the pre-
sleep instruction not to think about them.
As mentioned above, field studies using questionnaires clearly indicate
that there is an incorporation of waking-life events into dreams: about
50–70% of the participants, for example, stated that TV consumption or
reading books has affected their dreams (Lambrecht et al. 2013). Computer
games like Tetris or alpine racer and others have shown a strong effect on
subsequent dreams (Gackenbach et al. 2011; Stickgold et al. 2000, 2001).
Spending time with personally relevant everyday activities like sports
for sport students, music for music students, or politics for politics students
is related to the percentage of dreams that include these topics (Kern et al.
2014; Schredl and Erlacher 2008; Vogelsang et al. 2016). The romantic
partner also plays a major role in dreams (Schredl 2001; Schredl and
Reinhard 2012; Selterman et al. 2012). Interestingly, emotions related to
friends met during the day had the strongest correlations with dream
emotions—much more than emotions related to academic studies (Schredl
and Reinhard 2009–2010), indicating that social interactions during the
day have a considerable impact on dreaming.
Very stressful, traumatic events also affect subsequent dream content
most severely; recurrent nightmares of the trauma are a hallmark symptom
of posttraumatic stress disorder (PTSD) (Wittmann et al. 2007). The effects
of experiences related to the 9-11 terror attacks (Bulkeley and Kahan 2008),
sexual assault (Krakow et al. 1995), childhood sexual abuse (DeDonato
et al. 1996), kidnapping (Terr 1981, 1983), accidents (Mellman et al. 2001;
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 81
Wittmann et al. 2010), and war (Kramer et al. 1984; Sandman et al. 2013;
Schredl and Piel 2004) on dreams can be detected even decades after the
experiences in waking life.
In a diary study (Schredl 2006) the participants were instructed to keep
a diary over a two-week period and record the five most important events
of the day and rate their emotional intensity and valence (two five-point
scales). The participants also recorded their dreams and evaluated whether
one of the recorded events of the previous days showed up in the dream.
The emotional intensity and valence of the incorporated events was com-
pared with the other recorded events of the same day. The findings indi-
cated that emotional intensity was higher for incorporated events compared
to not incorporated events but the emotional valence of the waking-life
event had no effect (Schredl 2006). The study of Malinowski and Horton
(2014a) replicated this finding, emotional intensity but not stressfulness
was crucial for the incorporation of the waking-life event into subsequent
dreams. From a methodological viewpoint, it seems to be important to
use a design in which the emotional intensity of the waking-life event will
be rated before it shows up in the dream, that is, the approach of retro-
spectively rating the emotionality of events that resurfaced in the dream
(e.g., Vallat et al. 2017) might be biased by hindsight: I dreamed about
this, therefore it must be important.
Overall, the field studies and trauma studies indicate that emotional
intensity might be one of the most crucial factors affecting continuity
between waking and dreaming, that is, emotionally more intense
waking-life experiences are more likely to be incorporated into subsequent
dreams than less intense experiences.
Thematic continuity
Emotional continuity
Metacognitive continuity
Continuity of formal characteristics, for example, bizarreness
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 83
(Schredl 2008c). These few examples highlight that thematic and emo-
tional continuity must be studied differently: on the one hand, dream con-
tent analysis is the method to work with if the researcher is looking for
thematic continuity, on the other hand, measuring dream emotions with
self-rating scales are more appropriate to study emotional continuity.
Whereas some researchers (Hobson and Voss 2011; Rechtschaffen
1978) highlighted the deficiency of higher cognitive processing in dream-
ing Purcell, Mullington, Moffit, Hoffmann, and Pigeau (1986) and
Kahan, LaBerge, Levitan, and Zimbardo (1997) were able to demonstrate
that self-reflectiveness and metacognitions (e.g., thinking about different
options to act, being concerned about the impression made, or thinking
about the own thoughts, feelings, attitudes, behavior) are present in
dreams, maybe not as often as in waking. The typical dream theme “being
inappropriately dressed” (Griffith et al. 1958) is illustrating that the think-
ing about what others think about oneself being not dressed appropriately
or being totally nude is the major concern of the dreamer. Based on
research showing that meditating, being mindful during waking is linked
to lucid dream frequency and lucid dream control (Reed 1978; Stumbrys
and Erlacher 2016; Stumbrys et al. 2015) Stumbrys (2011) proposed a
continuity in self-reflective awareness, that is, persons who are self-reflective
during waking (e.g., by training mindfulness) are also more self-reflective
in dreams.
The last type of continuity concerns formal aspects of dreaming, for
example, schizophrenic patients who often show a formal thought disor-
der (incoherent thinking) also report more bizarre dreams (Schredl and
Engelhardt 2001). The style of thinking might affect specific dream char-
acteristics. However, carrying out these types of studies is very tricky as the
person can only report the dream while being awake, for example, in the
case of the patient with schizophrenia it is difficult to differentiate whether
the reporting of the dream is incoherent or the dream experience itself.
Future research is necessary to investigate this type of continuity in a more
detailed way.
As the continuity hypothesis does not make any claims regarding pos-
sible functions of dreaming, it is nevertheless interesting to ask the ques-
tion whether research done in this area might be helpful in speculating
about possible function(s) of dreaming (see Chap. 9).
The research regarding the temporal references of dream elements (see
above) indicates that new information is mixed with experiences from the
distant past. In addition, dreams are creative, that is, they form new asso-
ciations instead of just replaying daytime experiences (Hartmann 2011).
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 85
found in N1 sleep and REM sleep (Ibanez et al. 2009). In the study of
Campbell and Muller-Gass (2011) auditory stimuli that are only slightly
above hearing threshold appear to be processed extensively during a
200–400 milliseconds interval in both NREM and REM sleep. From
everyday anecdotes it is known that external stimuli (buzzer, telephone
ringing, snoring) can also be incorporated into the dream, that is, a very
complex processing of external stimuli can occur. A very famous example is
the stimulus incorporation of a piece of his wooden bed top falling on the
neck of the sleeper, Alfred Maury (1861). He dreamed that he will be
beheaded by the blade of a guillotine; the external stimulus was trans-
formed in a way that it fit into the dream plot which was about the French
revolution.
In Table 4.6, selected dream studies applying different types of stimuli
are listed. The standard approach is as follows: the sleeper is monitored via
polysomnography, if she/he is in REM sleep for about 5–10 minutes, the
stimulation is applied. The continuous EEG recording is important to
ensure that the person is not awakened by the stimulus, but it must have
an effect on the organism—above the perception threshold (Koulack
Dream: I dreamed I was in Golden Gate Park. I was walking by some gar-
denias. They were just opening. All of a sudden, I could smell the gardenias,
but they smelled like lemons instead of gardenias. (Stimulus: freshly cut
lemon; Trotter et al. 1988, p. 95)
Dream: Another women and I were inside a small self-service store, and we
were just about to get to the cashier. It was about whether I buy another
liquid to gargle with. And we kept walking around the store, and every time
I took a step with my right foot, it squeaked like an old door. It was like a
regular whistle sound, so that, with every step I took, it was as if I squeaked
like an old piece of furniture. And somehow I tried to fix that with the gargle
water. (Strauch and Meier 1996, p. 179)
The stimulus was incorporated into the dream but was not recognized
as weeping (Strauch and Meier 1996). For this dream the assumption that
the stimulus was incorporated and transformed seems quite plausible. The
question of what transformations of the stimulus are still acceptable is a
critical one: if the coding rules are too broad every dream might have
some form of reference to the stimulus. This methodological issue can be
dealt with by introducing a control condition, that is, comparing the
dreams after stimulation with dreams obtained from REM periods with-
out stimulation. It is necessary to elicit these control dreams within the
same study as, for example, participating in an olfactory study might also
show up in control dreams including some references to odors (Schredl
et al. 2009). Nielsen (1993) who coded direct and indirect incorporations
obtained 25% “incorporations” within the control dreams without prior
stimulation compared to 60% of the stimulated dreams. In addition, it
would be desirable that the dreamer did not know whether at all or what
88 M. SCHREDL
Overall, the research on external stimuli clearly indicates that the brain
is processing external stimuli during sleep and even though stimuli show
an effect on dreams in an experimental setting, the majority of the dreams
recalled in the home setting seems to be “stimulus-free”.
Table 4.7 Gender differences in dream content (Hall and Van de Castle 1966)
Variable Men Women
(N = 500) (N = 500)
reported dreams of deceased persons more often in all four studies (Schredl
and Piel 2005).
On the other hand, some findings have not been confirmed, for exam-
ple, the results concerning dream emotions; if self-ratings of the dreamers
were analyzed, no differences between men and women were observed
(Schredl et al. 1998). This might be explained by the limited validity of
measuring dream emotions via external judges (see Sect. 3.6). Although
Hall and Domhoff (1963) and Hall (1984) stated that the higher male/
female percentage of the dream characters is ubiquitous (similar findings
across different cultures), more recent studies (Domhoff et al. 2005–2006;
Schredl and Keller 2008–2009; Schredl et al. 2010–2011) were not able
to detect this specific gender difference for two reasons: the preponder-
ance of male dream characters in men’s dreams compared to the balanced
ration of the dream characters’ gender in women’s dreams was only found
in single men and women but not in students with a steady romantic rela-
tionship (Schredl 2001), and another factor was age as the “ubiquitous”
gender differences was only found in young adults but not in persons with
age over 25 years (Schredl and Keller 2008–2009; Schredl et al.
2010–2011). These findings indicate that it might be problematic to gen-
eralize the results stemming from student samples.
Another interesting method to study gender differences in dreaming is
a matching design: The external judges were presented with 200 dream
reports from 100 men and 100 women (the order is random) and asked to
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 91
guess whether the dreamer’s sex is male or female. All obvious references
to the dreamer’s gender were removed, for example, girlfriend was changed
into girlfriend/boyfriend. As a kind of pre-training the judge read several
empirical articles about gender differences in dreaming. In the study of
Schredl, Schwenger, et al. (2004) Judge 1 matched 64.0% of the dreams
correctly (equivalent to an effect size of d = 0.28) and Judge 2 matched
64.5% of the dreams correctly (d = 0.29). If it were complete random
guessing the result would be 50%, so the judges could guess the dreamer’s
gender based on the information of one dream report better than chance;
on the other hand a lot of guesses were not correct. Subsequent studies
(Schredl 2008a; Schredl et al. 2010) replicated this finding.
Another interesting gender difference relates to the gender of dream
aggressors in bad dreams of children and adolescents (see Table 4.8).
For girls and boys strange male characters are the dream aggressors that
occur most often whereas women comprise only about 20% of the aggres-
sors (Schredl and Pallmer 1998). The high percentage of male strangers as
human aggressors in children’s dreams seems also to support the continu-
ity hypothesis of dreaming as criminal rates including homicide are much
higher for men compared to women (Broidy and Agnew 1997), that is,
the gender distribution of violent criminals in waking is also reflected in
the dreams of children and adolescents.
Based on the consistent findings regarding several gender differences in
dream content, the question arises how these gender differences in dream
content can be explained—as gender itself does not explain anything.
According to the continuity hypothesis (see Sect. 4.3) gender differences
in dream content should reflect corresponding gender differences in wak-
ing life. Meta-analyses for gender differences in sexuality (Oliver and Hyde
1993) and physical aggression (Eagly 1987) clearly indicate gender differ-
ences similar to the reported differences in dreams do occur in waking life;
men, for example, more often reported about engaging in sexual fantasies
during waking and think more often about physical aggression. Schredl,
Desch, et al. (2009) were able to demonstrate that the frequency of sexual
fantasies in waking correlated with the frequency of erotic dreams.
Whereas Hall (1984) speculated about the Oedipus complex as one
possible explanation for the preponderance of male dream characters in
men’s dreams (in contrast to the equal amount of men and women in
women’s dreams), Paul and Schredl (2012) reported that male/female
percentage of the dream characters correlated with the male/female per-
centage of waking-life social interactions, that is, the findings are in line
with the continuity hypothesis. As persons with partnership dream often
about the partner (mostly of the opposite sex) the male/female ratio
decreased for men and increased for women and, thus, did not show this
specific gender difference anymore (Schredl 2001). Similar, Lortie-Lussier,
Simond, Rinfret, and De Koninck (1992) demonstrated that working
women’s dreams showed more similarities with the “male” dream pattern
than those of housewives.
To summarize, these studies clearly indicate that gender difference in
dream content are reflecting gender differences in waking life and thus pro-
vide further support for the continuity hypothesis of dreaming. As many
studies in this field are based on student samples, it would be necessary to
study samples with a larger age range. Especially interesting will be longitu-
dinal studies in larger samples of children to study the critical age when
gender differences in dream recall and dream content are developing.
References
Agargün, M. Y., Kara, H., Bilici, M., Cilli, A. S., Telci, M., Semiz, Ü. B., &
Basoglu, C. (1999). The Van Dream Anxiety Scale: A subjective measure of
dream anxiety in nightmare sufferers. Sleep and Hypnosis, 1, 204–211.
Arnulf, I., Grosliere, L., Le Corvec, T., Golmard, J.-L., Lascols, O., & Duguet, A.
(2014). Will students pass a competitive exam that they failed in their dreams?
Consciousness and Cognition, 29, 36–47.
Aumann, C., Lahl, O., & Pietrowsky, R. (2012). Relationship between dream
structure, boundary structure and the Big Five personality dimensions.
Dreaming, 22(2), 124–135.
Baekeland, F., Resch, R., & Katz, D. (1968). Presleep mentation and dream
reports: I. Cognitive style, contiguity to sleep and time of the night. Archives of
General Psychiatry, 19, 300–311.
Barrett, D. (2001). The committee of sleep: How artists, scientists, and athletes use
dreams for creative problem-solving – And how you can too. New York: Crown.
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 93
Bell, A. P., & Hall, C. S. (1971). The personality of a child molester: An analysis of
dreams. Chicago: Aldine-Atherton.
Berger, R. J. (1963). Experimental modification of dream content by meaningful
verbal stimuli. British Journal of Psychiatry, 109, 722–740.
Bernstein, D. M., & Belicki, K. (1995). On the psychometric properties of retro-
spective dream content questionnaires. Imagination, Cognition and Personality,
15, 351–364.
Bernstein, D. M., Belicki, K., & Gonzales, D. (1995). The development and
assessment of the reliability and validity of a dream content questionnaire
(DCQ). Sleep Research, 25, 138.
Blagrove, M., Fouquet, N. C., Henley-Einion, J. A., Pace-Schott, E. F., Davies,
A. C., Neuschaffer, J. L., & Turnbull, O. H. (2011). Assessing the dream-lag
effect for REM and NREM stage 2 dreams. PLoS ONE, 6(10), e26708.
Blagrove, M., Henley-Einion, J., Barnett, A., Edwards, D., & Seage, C. H. (2011).
A replication of the 5–7 day dream-lag effect with comparison of dreams to
future events as control for baseline matching. Consciousness and Cognition,
20(2), 384–391.
Bokert, E. G. (1967). The effect of thirst and a related verbal stimulus on dream
reports. Philosophical Dissertation, New York University.
Botman, H. I., & Crovitz, H. F. (1989). Dream reports and autobiographical
memory. Imagination, Cognition and Personality, 9, 213–224.
Breger, L., Hunter, I., & Lane, R. W. (1971). The effect of stress on dreams.
New York: International Universities Press.
Broidy, L., & Agnew, R. (1997). Gender and crime: A general strain theory per-
spective. Journal of Research in Crime and Delinquency, 34(3), 275–306.
Bruni, O., Lo Reto, F., Recine, A., Ottaviano, S., & Guidetti, V. (1999).
Development and validation of a dream content questionnaire for school age
children. Sleep and Hypnosis, 1, 41–46.
Bryant, R. A., Wyzenbeek, M., & Weinstein, J. (2011). Dream rebound of sup-
pressed emotional thoughts: The influence of cognitive load. Consciousness and
Cognition, 20(3), 515–522.
Bulkeley, K., & Domhoff, G. W. (2010). Detecting meaning in dream reports: An
extension of a word search approach. Dreaming, 20, 77–95.
Bulkeley, K., & Kahan, T. L. (2008). The impact of September 11 on dreaming.
Consciousness and Cognition, 17, 1248–1256.
Campbell, K. B., & Muller-Gass, A. (2011). The extent of processing of near-
hearing threshold stimuli during natural sleep. Sleep, 34, 1243–1249.
Carskadon, M. A., Wyatt, J., Etgen, G., & Rosekind, M. R. (1989). Nonvisual
sensory experiences in dreams of college students. Sleep Research, 18, 159.
Cartwright, R. D., Bernick, N., Borowitz, G., & Kling, A. (1969). Effect of an
erotic movie on the sleep and dreams of young men. Archives of General
Psychiatry, 20, 262–271.
94 M. SCHREDL
Curci, A., & Rime, B. (2008). Dreams, emotions, and social sharing of dreams.
Cognition and Emotion, 22, 155–167.
de Jong, M. A., & Visser, P. (1983). Mood, dream content and secondary revision
after different pre-sleep stimuli. Sleep Research, 12, 175.
De Koninck, J., & Brunette, R. (1991). Presleep suggestion related to a phobic
object: Successful manipulation of reported dream affect. Journal of General
Psychology, 118, 185–200.
De Koninck, J., & Koulack, D. (1975). Dream content and adaption to a stressful
situation. Journal of Abnormal Psychology, 84, 250–260.
DeDonato, A., Belicki, K., & Cuddy, M. (1996). Rater’s abilities to identify indi-
viduals reporting sexual abuse from nightmare content. Dreaming, 6, 33–41.
Dement, W. C., & Wolpert, E. A. (1958). The relation of eye movements, body
motility and external stimuli to dream content. Journal of Experimental
Psychology, 44, 543–553.
Domhoff, G. W. (2003). The scientific study of dreams: Neural networks, cognitive
development and content analysis. Washington, DC: American Psychological
Association.
Domhoff, G. W. (2017). The invasion of the concept snatchers: The origins, dis-
tortions, and future of the continuity hypothesis. Dreaming, 27(1), 14–39.
Domhoff, G. W. (2018). The emergence of dreaming: Mind-wandering, embodied
simulation, and the default network. New York: Oxford University Press.
Domhoff, G. W., Meyer-Gomes, K., & Schredl, M. (2005–2006). Dreams as the
expression of conceptions and concerns: A comparison of German and American
college students. Imagination, Cognition & Personality, 25, 269–282.
Duffey, T. H., Wooten, H. R., Lamadue, C. A., & Comstock, D. C. (2004). The
effects of dream sharing on marital intimacy and satisfaction. Journal of Couple
and Relationship Therapy, 3, 53–68.
Eagly, A. H. (1987). Sex differences in social behavior: A social-role interpretation.
Hillsdale: Lawrence Erlbaum.
Eagly, A. H., & Steffen, V. J. (1986). Gender and aggressive behavior: A meta-
analytic review of the social psychology literature. Psychological Bulletin, 100,
309–330.
Erdelyi, M. H. (2017). The continuity hypothesis. Dreaming, 27(4), 334–344.
Erlacher, D., & Schredl, M. (2004). Dreams reflecting waking sport activities: A
comparison of sport and psychology students. International Journal of Sport
Psychology, 35, 301–308.
Fosse, M. J., Fosse, R., Hobson, J. A., & Stickgold, R. J. (2003). Dreaming and
episodic memory: A functional dissociation? Journal of Cognitive Neuroscience,
15, 1–9.
Foulkes, D., & Griffin, M. L. (1976). An experimental study of “creative dream-
ing”. Sleep Research, 5, 129.
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 95
Hartmann, E. (2010). The underlying emotion and the dream: Relating dream
imagery to the dreamer’s underlying emotion can help elucidate the nature of
dreaming. International Review of Neurobiology, 92, 197–214.
Hartmann, E. (2011). The nature and functions of dreaming. New York: Oxford
University Press.
Hartmann, E., & Basile, R. (2003). Dream imagery becomes more intense after
9/11/01. Dreaming, 13, 61–66.
Hearne, K. M. T. (1978). Lucid dreams: An electrophysiological and psychological
study. Doctoral dissertation, University of Liverpool.
Heermann, G. (1838). Beobachtungen und Betrachtungen über die Träume der
Blinden, ein Beitrag zur Physiologie und Psychologie der Sinne. Monatsschrift
für Medicin, Augenheilkunde und Chirurgie, 1, 116–180.
Henley-Einion, J. A., & Blagrove, M. T. (2014). Assessing the day-residue and
dream-lag effects using the identification of multiple correspondences between
dream reports and waking life diaries. Dreaming, 24(2), 71–88.
Hobson, J. A. (1988). The dreaming brain. New York: Basic Books.
Hobson, J. A., & McCarley, R. W. (1977). The brain as a dream state generator:
An activation-synthesis hypothesis of the dream process. American Journal of
Psychiatry, 134, 1335–1348.
Hobson, J. A., & Voss, U. (2011). A mind to go out of: Reflections on primary
and secondary consciousness. Consciousness and Cognition, 20, 993–997.
Hobson, J. A., Hoffman, S. A., Helfand, R., & Kostner, D. (1987). Dream
bizarreness and the activation-synthesis hypothesis. Human Neurobiology, 6,
157–164.
Hobson, J. A., Pace-Schott, E. F., & Stickgold, R. (2000). Dreaming and the
brain: Toward a cognitive neuroscience of conscious states. Behavioral and
Brain Sciences, 23, 793–842.
Hoelscher, T. J., Klinger, E., & Barta, S. G. (1981). Incorporation of concern- and
nonconcern-related verbal stimuli into dream content. Journal of Abnormal
Psychology, 90, 88–91.
Ibanez, A. M., Martin, R. S., Hurtado, E., & Lopez, V. (2009). ERPs studies of
cognitive processing during sleep. International Journal of Psychology, 44(4),
290–304.
Jung, C. G. (1979). Allgemeine Gesichtspunkte zur Psychologie des Traumes. In
C. G. Jung (Ed.), Gesammelte Werke Band 8: Die Dynamik des Unbewußten
(pp. 268–308). Olten: Walter.
Kahan, T. L., & Claudatos, S. (2016). Phenomenological features of dreams:
Results from dream log studies using the Subjective Experiences Rating Scale
(SERS). Consciousness and Cognition, 41, 159–176.
Kahan, T. L., LaBerge, S., Levitan, L., & Zimbardo, P. (1997). Similarities and
differences between waking and dreaming cognition: An exploratory study.
Consciousness and Cognition, 6, 132–147.
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 97
Kahn, E., Dement, W., Fisher, C., & Barmack, J. E. (1962). Incidence of color in
immediately recalled dreams. Science, 137, 1054–1055.
Kallmeyer, R. J., & Chang, E. C. (1997). The multidimensional dream inventory:
Preliminary evidence for validity and reliability. Perceptual and Motor Skills, 85,
803–808.
Kern, S., Auer, A., Gutsche, M., Otto, A., Preuß, K., & Schredl, M. (2014).
Relation between waking politic, music and sports related tasks and dream con-
tent in students of politics and psychology students. International Journal of
Dream Research, 7, 80–84.
Kerr, N. H., & Domhoff, G. W. (2004). Do the blind literally “see” in their
dreams? A critique of a recent claim that they do. Dreaming, 14, 230–233.
Kerr, N. H., Foulkes, D., & Schmidt, M. (1982). The structure of laboratory
dream reports in blind and sighted subjects. Journal of Nervous and Mental
Disease, 170, 286–294.
König, N., Heizmann, L. M., Göritz, A. S., & Schredl, M. (2017). Colors in
dreams and the introduction of color TV in Germany: An online study.
International Journal of Dream Research, 10, 59–64.
Köthe, M., & Pietrowsky, R. (2001). Behavioral effects of nightmares and their
correlations to personality patterns. Dreaming, 11, 43–52.
Koulack, D. (1969). Effects of somatosensory stimulation on dream content.
Archives of General Psychiatry, 20, 718–725.
Krakow, B., Tandberg, D., Barey, M., & Scriggins, L. (1995). Nightmares and
sleep disturbance in sexually assaulted women. Dreaming, 5, 199–206.
Kramer, M. (2007). The dream experience: A systematic exploration. New York:
Routledge.
Kramer, M., Schoen, L. S., & Kinney, L. (1984). The dream experience in dream-
disturbed Vietnam veterans. In B. A. Van der Kolk (Ed.), Posttraumatic stress
disorder: Psychological and biological sequelace (pp. 82–95). Washington, DC:
American Psychiatric Press.
Kröner-Borowik, T., Gosch, S., Hansen, K., Borowik, B., Schredl, M., & Steil, R.
(2013). The effects of suppressing intrusive thoughts on dream content, dream
distress and psychological parameters. Journal of Sleep Research, 22(5),
600–604.
Kroth, J., Gilbert, H., Guichard, A., & Quatman, T. (1999). Analysis of factor
structure in a dream inventory. Perceptual and Motor Skills, 89, 657–658.
LaBerge, S. P. (1985). Lucid dreaming. Los Angeles: Jeremy P. Tarcher.
Lambrecht, S., Schredl, M., Henley-Einion, J., & Blagrove, M. (2013). Self-rated
effects of reading, TV viewing and daily activities on dreaming in adolescents
and adults: The UK library study. International Journal of Dream Research, 6,
41–44.
Lauer, C., Riemann, D., Lund, R., & Berger, M. (1987). Shortened REM latency:
A consequence of psychological strain? Psychophysiology, 24, 263–271.
98 M. SCHREDL
Leslie, K., & Ogilvie, R. (1996). Vestibular dreams: The effect of rocking on
dream mentation. Dreaming, 6, 1–16.
Lortie-Lussier, M., Simond, S., Rinfret, N., & De Koninck, J. (1992). Beyond sex
differences: Family and occupational roles’ impact on women’s and men’s
dreams. Sex Roles, 26, 79–96.
Malinowski, J. E., & Horton, C. L. (2014a). Evidence for the preferential incor-
poration of emotional waking-life experiences into dreams. Dreaming, 24(1),
18–31.
Malinowski, J. E., & Horton, C. L. (2014b). Memory sources of dreams: The
incorporation of autobiographical rather than episodic experiences. Journal of
Sleep Research, 23, 441–447.
Marquardt, C. J., Bonato, R. A., & Hoffmann, R. F. (1996). An empirical inves-
tigation into day-residue and dream-lag effects. Dreaming, 6, 57–65.
Mathes, J., & Schredl, M. (2013). Gender differences in dream content: Are they
related to personality? International Journal of Dream Research, 6, 104–109.
Maury, A. (1861). Le sommeil et les reves. Paris: Didier.
McCarley, R. W., & Hoffman, E. (1981). REM sleep dreams and the activation-
synthesis hypothesis. American Journal of Psychiatry, 138, 904–912.
Meier, B. (1993). Speech and thinking in dream. In C. Cavallero & D. Foulkes
(Eds.), Dreaming as cognition (pp. 58–76). London: Harvester Wheatsheaf.
Mellman, T. A., David, D., Bustamante, V., Torres, J., & Fins, A. (2001). Dreams
in the acute aftermath of trauma and their relationship to PTSD. Journal of
Traumatic Stress, 14, 241–247.
Meumann, E. (1909). Über Lesen und Schreiben im Traume. Archiv für die
Gesamte Psychologie, 15, 380–400.
Nielsen, T. A. (1993). Changes in the kinesthetic content of dreams following
somatosensory stimulation of leg muscles during REM sleep. Dreaming, 3,
99–113.
Nielsen, T. A., & Powell, R. A. (1989). The ‘dream-lag’ effect: A 6-day temporal
delay in dream content incorporation. Psychiatric Journal of the University of
Ottawa, 14, 561–565.
Nielsen, T. A., & Powell, R. A. (1992). The day-residue and dream lag effects: A
literature review and limited replication of two temporal effects in dream for-
mation. Dreaming, 2, 67–77.
Nielsen, T. A., McGregor, D. L., Zadra, A. L., Ilnicki, D., & Ouellet, L. (1993).
Pain in dreams. Sleep, 16, 490–498.
Nielsen, T. A., Kuiken, D., Alain, G., Stenstrom, P., & Powell, R. A. (2004).
Immediate and delayed incorporations of events into dreams: Further replica-
tion and implication for dream function. Journal of Sleep Research, 13, 327–336.
Oliver, M. B., & Hyde, J. S. (1993). Gender differences in sexuality: A meta-
analysis. Psychological Bulletin, 114, 29–51.
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 99
Olsen, M. R., Schredl, M., & Carlsson, I. (2013). Sharing dreams: Frequency,
motivations, and relationship intimacy. Dreaming, 23(4), 245–255.
Paul, F., & Schredl, M. (2012). Male-female ratio in waking-life contacts and
dream characters. International Journal of Dream Research, 5, 119–124.
Paul, F., Schädlich, M., & Erlacher, D. (2014). Lucid dream induction by visual
and tactile stimulation: An exploratory sleep laboratory study. International
Journal of Dream Research, 7(1), 61–66.
Pigman, G. W. (2002). The dark forest of authors: Freud and nineteenth-century
dream theory. Psychoanalysis and History, 4, 141–165.
Powell, R. A., Nielsen, T. A., Cheung, J. S., & Cervenka, T. M. (1995). Temporal
delays in incorporation of events into dreams. Perceptual and Motor Skills, 81,
95–104.
Purcell, S., Mullington, J., Moffit, A., Hoffmann, R., & Pigeau, R. (1986). Dream
self-reflectiveness as a learned cognitive skill. Sleep, 9(3), 423–437.
Rahimi, S., Naghibi, S. M., Mokhber, N., Schredl, M., Assadpour, H., Ramezani
Farkhani, A., Nemati Karimoui, H. A., Mohajeri, S. M. R., Darvish, A.,
Naghibi, S. S., & Sadjadi, S. A. (2015). Sophisticated evaluation of possible
effect of distinct auditory stimulation during REM sleep on dream content.
International Journal of Dream Research, 8(2), 146–151.
Rechtschaffen, A. (1978). The single-mindedness and isolation of dreams. Sleep, 1,
97–109.
Rechtschaffen, A., & Buchignani, C. (1992). The visual appearance of dreams. In
J. S. Antrobus & M. Bertini (Eds.), The neuropsychology of sleep and dreaming
(pp. 143–155). Hillsdale: Lawrence Erlbaum.
Rechtschaffen, A., & Foulkes, D. (1965). Effect of visual stimuli on dream con-
tent. Perceptual and Motor Skills, 20, 1149–1160.
Reed, H. (1978). Meditation and lucid dreaming: A statistical relationship.
Sundance Community Dream Journal, 2, 237–238.
Revonsuo, A. (2000). The reinterpretation of dreams: An evolutionary hypothesis
of the function of dreaming. Behavioral and Brain Sciences, 23, 877–901.
Revonsuo, A., Tuominen, J., & Valli, K. (2015). The Avatars in the machine. In
T. K. Metzinger & J. M. Windt (Eds.), Open mind (pp. 1–28). Frankfurt am
Main: Mind Group.
Roffwarg, H. P., Herman, J. H., Bowe-Anders, C., & Tauber, E. S. (1978). The
effects of sustained alterations of waking visual input on dream content. In
A. M. Arkin, J. S. Antrobus, & S. J. Ellman (Eds.), The mind in sleep: Psychology
and psychophysiology (pp. 295–349). Hillsdale: Lawrence Erlbaum.
Roussy, F., Raymond, I., Gonthier, I., Grenier, J., & De Koninck, J. (1998).
Temporal references in manifest dream content: Confirmation of increased
remoteness as the night progresses. Sleep Supplement, 21, 285.
Sandman, N., Valli, K., Kronholm, E., Ollila, H. M., Revonsuo, A., Laatikainen,
T., & Paunio, T. (2013). Nightmares: Prevalence among the Finnish general
adult population and war veterans during 1972–2007. Sleep, 36, 1041–1050.
100 M. SCHREDL
Schredl, M., Schwenger, C., & Dehe, A. (2004). Gender differences in dreams: A
matching study. Counseling and Clinical Psychology Journal, 1, 61–67.
Schredl, M., Fuchedzhieva, A., Hämig, H., & Schindele, V. (2008). Do we think
dreams are in black and white due to memory problems? Dreaming, 18,
175–180.
Schredl, M., Atanasova, D., Hörmann, K., Maurer, J. T., Hummel, T., & Stuck,
B. A. (2009). Information processing during sleep: The effect of olfactory
stimuli on dream content and dream emotions. Journal of Sleep Research, 18,
285–290.
Schredl, M., Bocklage, A., Engelhardt, J., & Mingebach, T. (2009). Psychological
boundaries, dream recall, and nightmare frequency: A new Boundary
Personality Questionnaire (BPQ). International Journal of Dream Research, 2,
12–19.
Schredl, M., Desch, S., Röming, F., & Spachmann, A. (2009). Erotic dreams and
their relationship to waking-life sexuality. Sexologies, 18, 38–43.
Schredl, M., Hebel, M. E., Klütsch, R. C., & Liehe, L. J. (2009). The role of
mood congruency memory effects in dream recall: A pilot study. Dreaming, 19,
113–118.
Schredl, M., Riemann, D., & Berger, M. (2009). The effect of trimipramine on
dream recall and dream emotions in depressive outpatients. Psychiatry Research,
167, 279–286.
Schredl, M., Becker, K., & Feldman, E. (2010). Predicting the dreamer’s gender
from a single dream report: A matching study in a non-student sample.
International Journal of Dream Research, 3, 130–133.
Schredl, M., Paul, F., Lahl, O., & Göritz, A. S. (2010–2011). Gender differences
in dream content: Related to biological sex or sex role orientation? Imagination,
Cognition, and Personality, 30, 171–183.
Schredl, M., Berres, S., Klingauf, A., Schellhaas, S., & Göritz, A. S. (2014). The
Mannheim Dream questionnaire (MADRE): Retest reliability, age and gender
effects. International Journal of Dream Research, 7, 141–147.
Schredl, M., Hoffmann, L., Sommer, J. U., & Stuck, B. A. (2014). Olfactory
stimulation during sleep can reactivate odor-associated images. Chemosensory
Perception, 7, 140–146.
Schredl, M., Buscher, A., Haaß, C., Scheuermann, M., & Uhrig, K. (2015).
Gender differences in dream socialisation in children and adolescents.
International Journal of Adolescence and Youth, 20, 61–68.
Schredl, M., Kim, E., Labudek, S., Schädler, A., & Göritz, A. S. (2015). Factors
affecting the gender difference in dream sharing frequency. Imagination,
Cognition and Personality, 34(3), 306–316.
Schredl, M., Kälberer, A., Zacharowski, K., & Zimmermann, M. (2017). Pain
dreams and dream emotions in patients with chronic back pain and healthy
controls. Open Pain Journal, 10, 65–72.
DREAM BEHAVIOR AND DREAM CONTENT IN HEALTHY PERSONS 103
(1994) argued that their finding indicates that dreams are not limited to
REM periods (i.e., dreams obtained after REM awakenings might also
include NREM dream experiences) but the studies of Jovanovic (1967)
suggest that a new dream is starting at the onset of a REM period:
Participants who were awakened shortly (20 seconds) after the onset of
REM sleep reported the subjective experience of a new dream beginning.
In a similar way, dream reports stemming from awakenings directly after
gross body movements which occur regularly during sleep in general and
also in REM sleep included often an experience of a dream that just ended
(Dement and Wolpert 1958). Using the “Nightcap” device, Hobson and
Stickgold (1995) have demonstrated that dream report length after spon-
taneous awakenings in the home setting is related to the duration of REM
sleep prior to the awakening: REM durations of 0–15 minutes yielded a
mean report length of 220 words, for 15–30 minutes 330 words, and for
30–45 minutes 510 words. For the duration over 45 minutes the mean
word count decreased to 350 words, maybe a ceiling effect. It can also be
argued that the time estimates depend on the dream content. Indeed,
Moiseeva (1975) found time estimates of the dream experience strongly
related to REM sleep duration, but there was a marked overestimation if
the dreams were bizarre, intense, and vivid, that is, if the experience is
vivid, intense, and detailed, the estimated time intervals are longer.
Another approach to compare the subjectively experienced time during
dreaming and REM duration is to investigate the temporal patterns of the
incorporation of external stimuli into dreams. Dement and Wolpert
(1958) reported the following dream example:
The first part of the dream involved a rather complex description of acting
in a play. I was walking behind the leading lady, when she suddenly collapsed
and water was dripping on her. I ran over to her and felt water dripping on
my back and head. The roof was leaking. I was very puzzled why she fell
down and decided some plaster must have fallen on her. I looked up and
there was a hole in the roof. I dragged her over to the side of the stage and
began pulling the curtain. Just then I woke up. (p. 550)
In this example, cold water was sprayed on the back of the dreamer
10 minutes after the onset of the REM period. Exactly 30 seconds later he
was awakened. The duration of the action sequence between applying the
external stimuli and awaking (dragging the person to the side of the stage)
108 M. SCHREDL
is comparable to the duration that this action would take in waking life.
Relating the temporal pattern of eye movement to dream content
(Roffwarg et al. 1962) also supports a close connection between “dreamed”
time and “real” time (see Sect. 5.2).
Lucid dreaming also offers a very sophisticated tool to study the rela-
tionship between dreamed time and real time. LaBerge (1985) asked his
participants to perform a distinct eye movement pattern, then count to ten
and after that repeat the eye movement made in the beginning—in the
waking state and during a lucid dream. The measured durations amounted
to about 13 seconds whether the task carried out in waking life or in a
lucid dream. Erlacher, Schädlich, Stumbrys, and Schredl (2014) expanded
LaBerge’s study using different counting intervals, walking periods, and a
brief gymnastic routine including jumps, somersaults (see Table 5.1).
Overall, it took a little bit longer to perform the task in the lucid dream
compared to the waking state (Erlacher et al. 2014). Interestingly, the
ratios ([Link]) of the time spent with counting or walking is very sta-
ble—in waking and in a lucid dream.
The findings clearly indicate a relatively direct relationship between
subjectively experienced time within the dream and objectively measured
REM sleep duration. Considering the small number of studies in this field,
several questions are still unanswered, for example, the relationship
between dream content (full of action vs. mundane dreams) and time.
Table 5.1 Comparisons of times for different activities carried out in wakefulness
or during a lucid dream (Erlacher et al. 2014)
Time in Time in a lucid Difference in
wakefulness (s) dream (s) percentage (%)
Counting (N = 5)
Counting to 10 8.9 ± 1.8 11.1 ± 3.0 +24.7
Counting to 20 17.0 ± 4.2 22.4 ± 6.3 +31.8
Counting to 30 24.4 ± 5.5 30.5 ± 8.0 +25.0
Walking (N = 7)
Walking 10 steps 6.7 ± 0.3 10.6 ± 4.0 +58.2
Walking 20 steps 12.5 ± 0.6 18.3 ± 6.0 +46.4
Walking 30 steps 18.5 ± 0.9 28.6 ± 9.8 +54.6
Gymnastic routine 6.6 ± 0.1 8.1 ± 1.5 +23.2
(N = 8)
DREAM CONTENT AND PHYSIOLOGY 109
The fact that the interviewer did not predict relatively small eye move-
ments (reading word by word within the line) can be explained by the
problem to detect such eye movements or the position of the eyeballs by
the commonly used sleep recording machines. The corresponding EOG
pattern of the above-cited example showed three small but distinct eye
movements to the left (22 seconds, 8 seconds, and 0.5 seconds prior to
the awakening). Overall, 80% of the clearly recalled dream actions corre-
sponded with the EOG recording in this study (Roffwarg et al. 1962). In
patients with REM sleep behavior disorder (see Sect. 6.6.4), Leclair-
Visonneau, Oudiette, Gaymard, Leu-Semenescu, and Arnulf (2010)
showed that the recorded eye movements were very often in sync with the
movements, for example, grabbing an imagined object (these patients act
out their dreams due to a loss of muscle atonia in REM sleep).
Interestingly, a direct relationship between eye movements within the
dream and the EOG recording was reported by lucid dream researchers
(Hearne 1978; LaBerge 1980). The participants were instructed to carry
out three large eye movements from the left to the right and backwards if
DREAM CONTENT AND PHYSIOLOGY 111
she/he is aware that she/he was dreaming. These eye movement patterns
were easily detectable out of the regularly occurring eye movements of the
REM period in almost 100% of the cases (N = 30 dreams; LaBerge et al.
1981).
To summarize, there seems to be a relationship between dream content
and eye movements (“scanning” hypothesis), however, it is not clear how
“tight” this relationship is, that is, whether all eye movements occurring in
REM sleep are related directly to dreamed gaze shifts. Hobson et al.
(2000) hypothesized that some of eye movements were caused by brain-
stem activity and Herman et al. (1984) have pointed out that predicting
eye movements based on a dream report can be a very difficult and error-
prone task, for example, eye movement while scanning non-moving
objects. In addition, other findings, for example, that congenitally blind
persons also have eye movements during REM sleep without having visual
dream imagery (Gross et al. 1965) or the occurrence of visual dreaming
during NREM sleep (e.g., Antrobus 1983), are not in line with the “scan-
ning hypothesis”. Thus, the relationship between dreamed eye move-
ments and real eye movements seems to be a complex one.
sleep (high EMG activity) obtaining a detailed dream report which often
includes communication and out of NREM sleep (low EMG activity) with
poor dream recall.
In the study of Wolpert (1960) dream reports were categorized into
active (many limb movements during the dream) and passive dreams. For
34 dream reports, the concordance between EMG activity (high vs. low)
and the dream action (active vs. passive) was high (74% of the cases;
p < 0.005). In two subsequent studies (Gardner et al. 1975; Grossman
et al. 1972), it was possible to differentiate between increased activity of
the arms during the dream (e. g. playing guitar) and leg activity (e. g.
walking). In a lucid dream hand clenching was related to muscle twitches
of the right respective left fist depending on the hand that was clenched in
the dream (LaBerge et al. 1981). These findings indicate that small muscle
twitches are related to the dream—supported by the findings in patients
with REM sleep behavior disorder (Valli et al. 2012) showing a relation
between dream content and actual movements during REM sleep.
Arkin et al. (1970) have investigated the relationship between sleep
talking and dream content. The following dream example was obtained by
awakening the sleeper after he had uttered audibly the sentence “Uh—
sniff—um—Argentina’s is a long way away—6000 miles”:
Dream example: I was dreaming about this girl I used to go out with last
summer and she’s from Argentina—and uh—I uh, I don’t know, see I—
can’t remember exactly what I was thinking but I uh—told her I’d go down
there to see her but, I don’t know, I can’t remember exactly what I was
thinking. So that seems to be in my mind. (p. 386; Arkin et al. 1970)
stages (Rechtschaffen and Kales 1968). Typically only two central EEG
sites (C3, C4) were recorded, but this was expanded to six electrodes
(F3, F4, C3, C4, O1, O2), that is, including occipital and frontal areas
(American Academy of Sleep Medicine 2007). However, this small num-
ber of electrodes does not allow any source location (brain mapping)
based on the surface EEG signals, therefore, more recent studies (e.g.,
Siclari et al. 2017) used high-density EEG systems with 256 elec-
trodes. But systematic studies using brain mapping based on high-den-
sity EEG in relation to dream content have not yet been carried out.
Several neuroimaging studies of REM sleep (overview: Desseilles et al.
2011) found, for example, a decrease of activation of the dorsolateral pre-
frontal cortex and an increased activity of the amygdala. These differences
were linked to dream characteristics like dream bizarreness as the dorsolat-
eral prefrontal cortex is associated with planning and self-reflection and
the presence of intense emotions in dreams because this would reflect the
activated emotional processing circuit of which the amygdala is a part
(Desseilles et al. 2011). However, it has to be emphasized that these plau-
sible correspondences between specific brain activation and dream features
have not yet been tested empirically using imaging techniques, that is, is
dream bizarreness correlated with the activation level of the dorsolateral
prefrontal cortex? So far, there is only a small number of EEG studies link-
ing dream content to brain activation.
In a general and solely qualitative way, Moiseeva (1975) stated that the
EEG pattern accompanying bizarre and emotional intense dreams is dif-
ferent from the pattern of neutral dreams. Zadra and Nielsen (1996) who
analyzed the EEG pattern of strong negatively toned dreams have found
differences in the central, parietal, and occipital brain areas (more alpha
activity) and suggested that this activation reflects intense visual imagery
(occipital area) and motor activity in the dream (central area). A similar
result was reported by Gottschalk et al. (1991) who related the anxiety
level of the dream to the brain activity measured by PET. High levels of
anxiety were associated with high activation in the occipital, central, and
frontal lobe (the area which is associated with self-reflective thinking).
Etevenon and Guillou (1986) reported that left central brain activity
(motor cortex) was increased in two REM periods when the dreams
included intense activity of the right hand. There was a similar finding for
hand clenching in a lucid dream—using alpha suppression in the corre-
sponding motor cortex area (C3 or C4) as an indicator of activation
(Erlacher et al. 2003). As mentioned above, this was supported by a fMRI-
EEG study (Dresler et al. 2011).
DREAM CONTENT AND PHYSIOLOGY 117
References
American Academy of Sleep Medicine. (2007). The AASM manual for the scoring
of sleep and associated events: Rules, terminology, and technical specifications.
Westchester: American Academy of Sleep Medicine.
Antrobus, J. S. (1983). REM and NREM sleep reports: Comparison of word fre-
quencies by cognitive classes. Psychophysiology, 20, 562–568.
DREAM CONTENT AND PHYSIOLOGY 119
Arkin, A. M., Toth, M. F., Baker, J., & Hastey, J. M. (1970). The degree of con-
cordance between content of sleep talking and mentation recalled in wakeful-
ness. Journal of Nervous and Mental Disease, 151, 375–393.
Aserinsky, E., & Kleitman, N. (1953). Regularly occurring periods of eye motility
and concomitant phenomena during sleep. Science, 118, 273–274.
Aserinsky, E., Lynch, J. A., Mack, M. E., Tzankoff, S. P., & Hurn, E. (1985).
Comparison of eye motion in wakefulness and REM sleep. Psychophysiology, 22,
1–10.
Berger, R. J., & Oswald, I. (1962). Eye movement during active and passive
dreams. Science, 137, 601.
De Gennaro, L., Cipolli, C., Cherubini, A., Assogna, F., Cacciari, C., Marzano,
C., Curcio, G., Ferrara, M., Caltagirone, C., & Spalletta, G. (2011). Amygdala
and hippocampus volumetry and diffusivity in relation to dreaming. Human
Brain Mapping, 32(9), 1458–1470. [Link]
Dement, W. C., & Kleitman, N. (1957). Cyclic variations in EEG during sleep and
their relation to eye movements, body motility and dreaming.
Electroencephalography and Clinical Neurophysiology, 9, 673–690.
Dement, W. C., & Wolpert, E. A. (1958). The relation of eye movements, body
motility and external stimuli to dream content. Journal of Experimental
Psychology, 44, 543–553.
Desseilles, M., Dang-Vu, T. T., Sterpenich, V., & Schwartz, S. (2011). Cognitive
and emotional processes during dreaming: A neuroimaging view. Consciousness
and Cognition: An International Journal, 20(4), 998–1008.
Dresler, M., Koch, S. P., Wehrle, R., Spoormaker, V. I., Holsboer, F., Steiger, A.,
Sämann, P. G., Obrig, H., & Czisch, M. (2011). Dreamed movement elicits
activation in the sensorimotor cortex. Current Biology, 21, 1833–1837.
Dresler, M., Wehrle, R., Spoormaker, V. I., Koch, S. P., Holsboer, F., Steiger, A.,
Obrig, H., Samann, P. G., & Czisch, M. (2012). Neural correlates of dream
lucidity obtained from contrasting lucid versus non-lucid REM sleep: A com-
bined EEG/fMRI case study. Sleep, 35, 1017–1020.
Erlacher, D., Schredl, M., & LaBerge, S. (2003). Motor area activation during
dreamed hand clenching: A pilot study on EEG alpha band. Sleep and Hypnosis,
5, 182–187.
Erlacher, D., Schädlich, M., Stumbrys, T., & Schredl, M. (2014). Time for actions
in lucid dreams: Effects of task modality, length, and complexity. Frontiers in
Psychology, 4. [Link]
Etevenon, P., & Guillou, S. (1986). EEG cartography of a night of sleep and
dreams: A longitudinal study with provoked awakenings. Neuropsychobiology,
16, 146–151.
Fahrion, S. L. (1967). The relationship of heart rate and dream content in heart-
rate responders. Dissertation Abstracts, 27(9-B), 3307.
Firth, H., & Oswald, I. (1975). Eye movements and visually active dreams.
Psychophysiology, 12, 602–606.
120 M. SCHREDL
Hong, C. C., Jin, Y., Potkin, S. G., Buchsbaum, M., Wu, J. C., Callagham, G.,
Nudleman, K., & Gillin, J. C. (1996). Language in dreaming and regional
EEG alpha power. Sleep, 19, 232–235.
Hong, C. C., Potkin, S. G., Antrobus, J. S., Dow, B. M., Callaghan, G. M., &
Gillin, J. C. (1997). REM sleep eye movement counts correlate with visual
imagery in dreaming: A pilot study. Psychophysiology, 34, 377–381.
Horikawa, T., Tamaki, M., Miyawaki, Y., & Kamitani, Y. (2013). Neural decoding
of visual imagery during sleep. Science, 340(6132), 639–642.
Jouvet, M. (1999). The paradox of sleep – The story of dreaming. Cambridge, MA:
MIT Press.
Jovanovic, U. J. (1967). Einige Charakteristika des Traumbeginns. Psychologische
Forschung, 30, 281–306.
Kalat, J. W. (2014). Biological psychology. Independence: Wadsworth.
LaBerge, S. P. (1980). Lucid dreaming: An exploratory study of consciousness dur-
ing sleep. Doctoral dissertation, Stanford University.
LaBerge, S. P. (1985). Lucid dreaming. Los Angeles: Jeremy P. Tarcher.
LaBerge, S. P., Nagel, L. E., Dement, W. C., & Zarcone, V. P. (1981). Lucid
dreaming verified by volitional communication during REM sleep. Perceptual
and Motor Skills, 52, 727–732.
Leclair-Visonneau, L., Oudiette, D., Gaymard, B., Leu-Semenescu, S., & Arnulf,
I. (2010). Do the eyes scan dream images during rapid eye movement sleep?
Evidence from the rapid eye movement sleep behaviour disorder model. Brain,
133, 1737–1746.
Levin, R., & Nielsen, T. A. (2007). Disturbed dreaming, posttraumatic stress dis-
order, and affect distress: A review and neurocognitive model. Psychological
Bulletin, 133, 482–528.
Maquet, P., Peters, J.-M., Aerts, J., Delfiore, G., Deguelde, C., Luxen, A., &
Franck, G. (1996). Functional neuroanatomy of human rapid-eye-movement
sleep and dreaming. Nature, 383, 163–166.
Maury, A. (1861). Le sommeil et les reves. Paris: Didier.
Max, L. W. (1935). An experimental study of the motor theory of consciousness:
III. Action-current responses in deaf-mutes during sleep, sensory stimulation
and dreams. Journal of Comparative Psychology, 19, 469–487.
McGuigan, F. J., & Tanner, R. G. (1971). Covert oral behavior during conversa-
tional and visual dreams. Psychonomic Sciences, 23, 263–264.
Moiseeva, N. I. (1975). The characteristics of EEG activity and the subjective
estimation of time during dreams of different structure. Electroencephalography
and Clinical Neurophysiology, 38, 569–577.
Moody, R. A. (1989). The light beyond. New York: Bantam Book.
Pietrusky, F. (1922). Das Verhalten der Augen im Schlafe. Klinische Monatsblätter
für Augenheilkunde, 68, 355–366.
Rechtschaffen, A., & Kales, A. (1968). A manual of standardized terminology,
techniques and scoring system for sleep stages of human subjects. Washington, DC:
U. S. Public Health Service.
122 M. SCHREDL
Roffwarg, H. P., Dement, W. C., Muzio, J. N., & Fisher, C. (1962). Dream imag-
ery: Relationship to rapid eye movements of sleep. Archives of General
Psychiatry, 7, 235–258.
Rosenlicht, N., Maloney, T., & Feinberg, I. (1994). Dream report length is more
dependent on arousal level than prior REM duration. Brain Research Bulletin,
34, 99–101.
Schredl, M., & Erlacher, D. (2010). Is sleep-dependent memory consolidation of
a visuo-motor task related to dream content? International Journal of Dream
Research, 3, 74–79.
Schredl, M., Paul, F., Reinhard, I., Ebner-Priemer, U. W., Schmahl, C., & Bohus,
M. (2012). Sleep and dreaming in patients with borderline personality disor-
der: A polysomnographic study. Psychiatry Research, 200, 430–436.
Shimizu, A., & Inoue, T. (1986). Dreamed speech and speech muscle activity.
Psychophysiology, 23, 210–214.
Siclari, F., Baird, B., Perogamvros, L., Bernardi, G., LaRocque, J. J., Riedner, B.,
Boly, M., Postle, B. R., & Tononi, G. (2017). The neural correlates of dream-
ing. Nature Neuroscience, 20, 872–878.
Siegel, J. M. (2017). Rapid eye movement sleep. In M. Kryger, T. Roth, & W. C.
Dement (Eds.), Principles and practice of sleep medicine (6th ed., pp. 78–95).
Philadelphia: Elsevier.
Stegie, R., Baust, W., & Engel, R. R. (1975). Psychophysiological correlates in
dreams. In W. Koella (Ed.), Sleep 1974 (pp. 409–412). Basel: Karger.
Stoyva, J. M. (1965). Finger electromyographic acitivity during sleep: Its relation
to dreaming in deaf and normal subjects. Journal of Abnormal Psychology, 70,
343–349.
Stumbrys, T., Erlacher, D., & Schredl, M. (2013). Testing the involvement of the
prefrontal cortex in lucid dreaming: A tDCS study. Consciousness and Cognition,
22(4), 1214–1222.
Valli, K., Frauscher, B., Gschliesser, V., Wolf, E., Falkenstetter, T., Schönwald,
S. V., Ehrmann, L., Zangerl, A., Marti, I., Boesch, S. M., Revonsuo, A., Poewe,
W., & Högl, B. (2012). Can observers link dream content to behaviours in
rapid eye movement sleep behaviour disorder? A cross-sectional experimental
pilot study. Journal of Sleep Research, 21, 21–29. [Link]
org/10.1111/j.1365-2869.2011.00938.x.
Voss, U., Holzmann, R., Hobson, A., Paulus, W., Koppehele-Gossel, J., Klimke,
A., & Nitsche, M. A. (2014). Induction of self awareness in dreams through
frontal low current stimulation of gamma activity. Nature Neuroscience, 17(6),
810–812.
Wolpert, E. A. (1960). Studies in psychophysiology of dreams: II. An electromyo-
graphic study of dreaming. Archives of General Psychiatry, 2, 231–241.
Zadra, A. L., & Nielsen, T. A. (1996). EEG spectral analyses of REM nightmares
and anxiety dreams (abstract). Conference of the international association for
the study of dreams, Berkeley.
CHAPTER 6
6.1 Introduction
Three motives have stimulated the investigation of dreaming in mental
disorders. First, the dream state itself was conceptualized by several theo-
rists as a mental disorder, hallucinating something that is not there
(Hobson 1997), and, secondly, hallucinations of schizophrenic patients
have been conceptualized as breakthroughs of dreams into the waking
state (Noble 1950). Third, many clinicians since Sigmund Freud have
attempted to use dreams in the diagnosis and treatment of their patients
with various mental disorders (Pesant and Zadra 2004).
According to the continuity hypothesis different waking symptoms of
patients with different mental disorders should be reflected in the dream
reports of these patients. As mental disorders are often accompanied by
significant distress, the continuity hypothesis would predict more negative
dream emotions. In Table 6.1, the prevalence rates of the nightmare dis-
order for different patient groups are depicted—the comparison to the
figure of about 5% found in the general population (Levin and Nielsen
2007) indicates that patients with various mental disorders experience
more often negatively toned dreams.
Several extensive reviews about dreaming in patients with mental disor-
ders have been published (Kramer 2000, 2010; Kramer and Nuhic 2007;
Kramer and Roth 1978; Mellen et al. 1993; Skancke et al. 2014) showing
that the main focus has been on schizophrenia, depression, PTSD, and
eating disorders. PTSD will not be reviewed in this section, as dreams,
When the big mid-day meal arrived upstairs it was not wrapped up separately
for each patient with anorexia but was in one large bowl. Each one has to
take one part so that everyone gets the same amount. Of course everyone
took less and I got the biggest part. This was so stupid because this part had
the most calories in it. The supervisors did not believe me when I said that
it is too much but then I did not eat it. (Schredl and Montasser 1999)
This dream is clearly affected by the hospital setting. Similarly, the find-
ing of more unknown persons or strangers in dreams of patients with
schizophrenia (Kramer and Roth 1973; Lusignan et al. 2009) might be
explained by being in a psychiatric ward where meeting unknown persons
(new patients, new nursing staff, visitors of other patients, etc.) each day is
common. In order to control the dream content analytic findings for such
confounders, the daily lives of each group have to be monitored and mea-
sured quite extensively.
126 M. SCHREDL
6.3 Depression
The common feature of depressive disorders is the presence of sad, empty,
or irritable mood, accompanied by other symptoms like diminished inter-
est or pleasure in almost all activities or pessimistic thoughts and a signifi-
cant distress or impairment in social, occupational, or other important
areas of functioning (American Psychiatric Association 2013). In addition
to unipolar depressive disorders, the DSM-5 includes bipolar disorders,
that is, depressive and manic (or hypomanic) phases occur in these patients.
The manic episode is characterized by abnormally elevated and expansive
DREAMS AND MENTAL DISORDERS 127
6.4 Schizophrenia
The key features of schizophrenia and other psychotic disorders are delu-
sions (fixed beliefs that are not changed by obvious counterfactual evi-
dence, for example, persecutory, religious, grandiose delusions),
hallucinations (most often auditory (voices)), disorganized thinking
(speech), and negative symptoms like diminished emotional expression or
anhedonia (American Psychiatric Association 2013).
Whereas dream recall frequency in schizophrenic patients seems not to
differ from healthy controls in a systematic way (Lusignan et al. 2009;
Michels et al. 2014), schizophrenic patients reported nightmares more
often (Lusignan et al. 2009; Michels et al. 2014; Okorome Mume 2009)
and the occurrence of nightmares were—in conjunction with insomnia—
related to an increased risk of suicide attempts (Li et al. 2016)—frequent
nightmares as an independent predictor of suicidal ideation has been
reported in non-clinical samples (e.g., Nadorff et al. 2013). Also patients
at high risk states for psychosis reported significantly more nightmares
than controls (Michels et al. 2014).
More bizarreness, and implausibility, in dreams of schizophrenics com-
pared to non-schizophrenics has been one of the most robust findings
(Kramer 2000). However, Scarone et al. (2008) and Lusignan et al.
(2009) did not find differences in dream bizarreness between schizo-
phrenics and controls, even though the waking mentation of schizophren-
ics was found to be more bizarre than that of controls. On the other hand,
DREAMS AND MENTAL DISORDERS 129
Noreika, Valli, Markkula, Seppälä, and Revonsuo (2010) found that the
schizophrenics’ dreams were more bizarre than healthy controls. Studies
focusing on formal aspects of the dream reports using graph analysis
(Mota et al. 2014; Mota et al. 2012) or textual analysis processing tech-
niques (Zanasi et al. 2011) were able to demonstrate that the waking-life
symptom thought disorder also can be detected in dream reports. On a
methodological note, it has to be considered that the distinction between
dream bizarreness and disorganized thinking and speech in waking is not
easy as the dreams are reported by the patients in their waking state, that
is, the thought disorder might affect the process of dream reporting but
not the dreaming process itself. The correlation between the question-
naire indices “paranoid ideation” and “psychoticism” with dream bizarre-
ness in schizophrenic patients and also in non-schizophrenic patients
(Schredl and Engelhardt 2001) might indicate that severity of psychotic
symptoms might be associated with dreaming itself as the non-
schizophrenic patient group did not suffer from a full-blown thought dis-
order. D’Agostino et al. (2013) reported that in two patients the topic of
their delusion (grandiosity, religious delusion) did show up in the dreams
of these patients, supporting the notion of continuity between waking and
dreaming.
Systematic studies of antipsychotic drugs (typical and atypical neurolep-
tics) on dream content are still lacking (Kramer and Nuhic 2007); the
reported correlation between severity of psychotic symptoms and dream
characteristics, like bizarreness (Schredl and Engelhardt 2001), would
indicate a normalization of dream content in the course of a successful
therapy.
Despite the very interesting topic of dreaming in schizophrenia (dream-
ing as a “normal” form of psychosis), many questions are still unanswered.
↑ heightened in patients compared to healthy controls, = comparable to healthy controls, --- not studied
132 M. SCHREDL
6.6.1 Insomnia
The essential feature of chronic insomnia disorder is a frequent and persis-
tent difficulty in initiating or maintaining sleep that results in a clinically
significant distress and impairment in important areas of functioning
(American Academy of Sleep Medicine 2014). The prevalence of chronic
insomnia disorder in the general population is quite high (about 10%) and
associated risk factors are stressors, personality factors like neuroticism,
and medical illnesses (American Academy of Sleep Medicine 2014).
Using REM awakenings in the sleep laboratory patients with insomnia
was comparable to healthy controls regarding dream recall (Ermann 1995;
Pérusse et al. 2016). However, home dream recall was elevated in insom-
nia patients compared to healthy controls (Schredl et al. 1998) with the
statistical analysis indicating the idea that this dream recall frequency dif-
ference is explained by heightened frequency of nocturnal awakenings in
patients with insomnia. This is in line with the positive correlation between
frequency of nocturnal awakenings and dream recall frequency in healthy
persons (Schredl et al. 2003).
Several studies (Ohayon et al. 1997; Pagel and Shocknesse 2007;
Schredl 2009) found that persons with insomnia complained about night-
mares more often than patients without insomnia or healthy controls.
Nightmare frequency was directly related to insomnia severity (Schredl
2009). As stress and negative life-events can trigger insomnia, the increase
in nightmare frequency and the more negatively toned dreams in patients
with insomnia are in line with the continuity hypothesis of dreaming, that
is, dreams reflects the waking-life stressors that had affected sleep nega-
tively. The negative dream emotions correlated directly with the number
of waking-life problems (Schredl et al. 1998). In a group of 37 patients
with insomnia, negative dream themes correlated with the severity of
early-life maltreatment experiences, that is, even years after the stressful
experience the dreams are affected, and one might speculate whether these
negative life-events did also play a role in insomnia etiology in this patient
group (Schäfer and Bader 2009).
DREAMS AND MENTAL DISORDERS 133
During the dream I felt tied up or chained. I saw thick ropes around my
arms and was not able to move. I experienced the fear of suffocation without
being able to cope with the situation. Powerlessness and also resignation
came up. (Patient with sleep apnea, male, 39 years, respiratory disturbance
index (RDI): 68.1 apneas per hour, maximal drop of blood oxygen satura-
tion: 43%; Schredl 1998b, p. 295)
DREAMS AND MENTAL DISORDERS 135
I was diving without oxygen tanks and was gasping for breath. The way
to the surface was far and I managed it just in time. After waking up I really
gasped for breath. (male, 39 years, REM-sleep associated sleep apneas, RDI:
71.8, oxygen saturation nadir: 68%; Schredl et al. 2006, p. 207)
6.6.3 Narcolepsy
Narcolepsy is characterized by excessive sleepiness (irrepressible need to
sleep or lapses into sleep) and diagnosed by carrying out a multiple sleep
latency test with five short sleep periods during the day in which the
patient falls asleep quickly (mean latency below 8 minutes) and shows two
or more sleep onset REM periods (onset of REM sleep within 15 minutes)
(American Academy of Sleep Medicine 2014). In many narcolepsy patients
cataplexies (sudden loss of muscle tone with retained consciousness often
triggered by strong emotions, e.g., laughing) and other REM-sleep asso-
136 M. SCHREDL
I dreamt that I stepped out of the bright light of the lamp and slipped into
another time period. I met my grandfather who I had never seen in my wak-
ing life and saw other persons from my hometown, much younger than
today. With the help of friends I managed to travel back to the present time.
I even brought some stuff from the past with me which my mother identi-
fied as her former belongings. (p. 106)
DREAMS AND MENTAL DISORDERS 137
I was a halfback playing football, and after the quarterback received the ball
from the center he lateraled it sideways to me and I’m supposed to go around
end und cut back over tackle and—this is very vivid—as I cut back over tackle
there is this big 280-pound tackle waiting, so I, according to football rules,
was to give him my shoulder and bounce him out of the way, supposedly, and
when I came to I was standing in front of our dresser and I had knocked
lamps, mirrors, and everything of the dresser, hit my head against the wall
and my knee against the dresser (p. 294; Schenck et al. 1986).
dream recall, suggesting that they also experienced dreams but had prob-
lems to remember them upon awakening (Herlin et al. 2015). In 19
sequences with motor behavior in REM sleep most of the parallel recorded
eye movements (82%) were related to the actual movement, for example,
grabbing a fictive object, climbing a ladder (Leclair-Visonneau et al.
2010), also indicating that studying dreaming of patients with RBD in
detail offers a new approach to study the relationship between physiology
and dream content.
References
Amara, A. W., & Maddox, M. H. (2017). Epidemiology of sleep medicine. In
M. Kryger, T. Roth, & W. C. Dement (Eds.), Principles and practice of sleep
medicine (6th ed., pp. 627–637). Philadelphia: Elsevier.
American Academy of Sleep Medicine. (2014). The international classification of
sleep disorders (ICSD-3). Darien: AASM.
American Psychiatric Association. (2013). Diagnostic and statistical manual of
mental disorders: DSM-5. Washington, DC: American Psychiatric Association.
Anelli, M. M., Fantini, M., Erzegovesi, S., Bellodi, L., & Ferini-Strambi, L.
(2007). Dreams and sleep pattern in women with bulimia nervosa. Sleep
Supplement, 30, A381–A382.
Armitage, R., Rochlen, A., Fitch, T., Trivedi, M., & Rush, A. J. (1995). Dream
recall and major depression: A preliminary report. Dreaming, 5, 189–198.
Beauchemin, K. M., & Hays, P. (1995). Prevailing mood, mood changes and
dreams in bipolar disorder. Journal of Affective Disorders, 35, 41–49.
Beauchemin, K. M., & Hays, P. (1996). Dreaming away depression: The role of
REM sleep and dreaming in affective disorders. Journal of Affective Disorders,
41, 125–133.
Beck, A. T., & Hurvich, M. S. (1959). Psychological correlates of depression:
I. Frequency of “masochistic” dream content in a private practice sample.
Psychosomatic Medicine, 1, 50–55.
Beck, A. T., & Ward, C. H. (1961). Dreams of depressed patients. Archives of
General Psychiatry, 5, 462–467.
Boerner, J. (1855). Das Alpdrücken: Seine Begründung und Verhütung. Würzburg:
Carl Joseph Becker.
Brink, S. M., & Allan, J. A. B. (1992). Dreams of anorexic and bulimic women: A
research study. Journal of Analytical Psychology, 37, 275–297.
Brink, S. M., Allan, J. A., & Boldt, W. (1995). Symbolic representation of psycho-
logical states in the dream of women with eating disorders. Canadian Journal
of Counseling, 29, 332–344.
Carrasco, E., Santamaria, J., Iranzo, A., Pintor, L., De Pablo, J., Solanas, A.,
Kumru, H., Martinez-Rodrigez, J. E., & Boget, T. (2006). Changes in dream-
140 M. SCHREDL
Giordano, P. L., & Spoto, G. (1977). Patient’s reports of their own sleep and
dream experience in psychopharmacological sleep research and treatment.
Activitas Nervose Superior, 19(Supplement 2), 370.
Glucksman, M. L., & Kramer, M. (2017). Manifest dream content as a predictor
of suicidality. Psychodynamic Psychiatry, 45(2), 175–185.
Godin, I., Montplaisir, J., Gagnon, J.-F., & Nielsen, T. (2013). Alexithymia asso-
ciated with nightmare distress in idiopathic REM sleep behavior disorder. Sleep:
Journal of Sleep and Sleep Disorders Research, 36(12), 1957–1962.
Godin, I., Montplaisir, J., & Nielsen, T. (2015). Dreaming and nightmares in
REM sleep behavior disorder. Dreaming, 25(4), 257–273.
Gross, M., & Lavie, P. (1994). Dreams in sleep apnea patients. Dreaming, 4,
195–204.
Hauri, P. (1976). Dreams in patients remitted from reactive depression. Journal of
Abnormal Psychology, 85, 1–10.
Herlin, B., Leu-Semenescu, S., Chaumereuil, C., & Arnulf, I. (2015). Evidence
that non-dreamers do dream: A REM sleep behaviour disorder model. Journal
of Sleep Research, 24(6), 602–609.
Hobson, J. A. (1997). Dreaming as delirium: A mental status examination of our
nightly madness. Seminars in Neurology, 17, 121–128.
Jackson, C., Beumont, P. J., Thornton, C., & Lennerts, W. (1993). Dreams of
death: Von Weizäcker’s dreams in so-called endogeneous anorexia: A research
note. International Journal of Eating Disorders, 13, 329–332.
Jouvet, M. (1999). The paradox of sleep – The story of dreaming. Cambridge, MA:
MIT Press.
Krakow, B., & Zadra, A. L. (2010). Imagery rehearsal therapy: Principles and
practice. Sleep Medicine Clinics, 5, 289–298.
Kramer, M. (2000). Dreams and psychopathology. In M. H. Kryger, T. Roth, &
W. C. Dement (Eds.), Principles and practice of sleep medicine (pp. 511–519).
Philadelphia: W. B. Saunders.
Kramer, M. (2010). Dream differences in psychiatric patients. In S. R. Pandi-
Perumal & M. Kramer (Eds.), Sleep and mental illness (pp. 375–382).
Cambridge: Cambridge University Press.
Kramer, M., & Nuhic, Z. (2007). A review of dreaming by psychiatric patients: An
update. In S. Pandi, R. Ruoti, & M. Kramer (Eds.), Sleep and psychosomatic
medicine (pp. 137–155). New York: Taylor and Francis.
Kramer, M., & Roth, T. (1973). A comparison of dream content in laboratory
dream reports of schizophrenic and depressed patient groups. Comprehensive
Psychiatry, 14, 325–329.
Kramer, M., & Roth, T. (1978). Dreams in psychopathologic patient groups. In
R. L. Williams & I. Karacan (Eds.), Sleep disorders: Diagnosis and treatment
(pp. 323–349). New York: Wiley.
142 M. SCHREDL
Kramer, M., Whitman, R. M., Baldridge, B. J., & Ornstein, P. H. (1968). Drugs
and dreams: III. The effects of imipramine on the dreams of the depressed.
American Journal of Psychiatry, 124, 1385–1392.
Leclair-Visonneau, L., Oudiette, D., Gaymard, B., Leu-Semenescu, S., & Arnulf,
I. (2010). Do the eyes scan dream images during rapid eye movement sleep?
Evidence from the rapid eye movement sleep behaviour disorder model. Brain,
133, 1737–1746.
Levin, R., & Nielsen, T. A. (2007). Disturbed dreaming, posttraumatic stress dis-
order, and affect distress: A review and neurocognitive model. Psychological
Bulletin, 133, 482–528.
Li, S. X., Lam, S. P., Zhang, J., Yu, M. W. M., Chan, J. W. Y., Chan, C. S. Y.,
Espie, C. A., Freeman, D., Mason, O., & Wing, Y.-K. (2016). Sleep distur-
bances and suicide risk in an 8-year longitudinal study of schizophrenia-
spectrum disorders. Sleep, 39(6), 1275–1282.
Limosani, I., D’Agostino, A., Manzone, M. L., & Scarone, S. (2011). Bizarreness
in dream reports and waking fantasies of psychotic schizophrenic and manic
patients: Empirical evidences and theoretical consequences. Psychiatry Research,
189(2), 195–199.
Lusignan, F.-A., Zadra, A. L., Dubuc, M.-J., Daoust, A.-M., Mottard, J.-P., &
Godbout, R. (2009). Dream content in chronically-treated persons with
schizophrenia. Schizophrenia Research, 112, 164–173.
MacFarlane, J. G., & Wilson, T. L. (2006). A relationship between nightmare
content and somatic stimuli in a sleep-disordered population: A preliminary
study. Dreaming, 16, 53–59.
Mayer, G., Kesper, K., Peter, H., Ploch, T., Leinweber, T., & Peter, J.-H. (2002).
Untersuchung zur Komorbidität bei Narkolepsiepatienten. Deutsche
Medizinische Wochenschrift, 127, 1942–1946.
Mazzetti, M., Bellucci, C., Mattarozzi, K., Plazzi, G., Tuozzi, G., & Cipolli, C.
(2010). REM-dreams recall in patients with narcolepsy-cataplexy. Brain
Research Bulletin, 81, 133–140.
Mellen, R. R., Duffey, T. H., & Craig, S. M. (1993). Manifest content in the
dreams of clinical populations. Journal of Mental Health Counseling, 15,
170–183.
Michels, F., Schilling, C., Rausch, F., Eifler, S., Zink, M., Meyer-Lindenberg, A.,
& Schredl, M. (2014). Nightmare frequency in schizophrenic patients, healthy
relatives of schizophrenic patients, patients at high risk states for psychosis, and
healthy controls. International Journal of Dream Research, 5, 9–13.
Mignot, E. (2017). Narcolepsy: Genetics, immunology, and pathophysiology. In
M. Kryger, T. Roth, & W. C. Dement (Eds.), Principles and practice of sleep
medicine (6th ed., pp. 855–872). Philadelphia: Elsevier.
Mota, N. B., Vasconcelos, N. A. P., Lemos, N., Pieretti, A. C., Kinouchi, O.,
Cecchi, G. A., Copelli, M., & Ribeiro, S. (2012). Speech graphs provide a
DREAMS AND MENTAL DISORDERS 143
Riemann, D., Löw, H., Schredl, M., Wiegand, M., Dippel, B., & Berger, M.
(1990). Investigations of morning and laboratory dream recall and content in
depressive patients during baseline conditions and under antidepressive treat-
ment with trimipramine. Psychiatric Journal of the University of Ottawa, 15,
93–99.
Ross, R. J., Ball, W. A., Sullivan, K. A., & Caroff, S. N. (1989). Sleep disturbances
as the hallmark of posttraumatic stress disorder. American Journal of Psychiatry,
146, 697–707.
Roth, B., & Bruhova, S. (1969). Dreams in narcolepsy, hypersomnia and dissoci-
ated sleep disorders. Experimental Medicine and Surgery, 27, 187–209.
Scarone, S., Manzone, M. L., Gambini, O., Kantzas, I., Limosani, I., D’Agostino,
A., & Hobson, J. A. (2008). The dream as a model for psychosis: An experi-
mental approach using bizarreness as a cognitive marker. Schizophrenia Bulletin,
34, 515–522.
Schäfer, V., & Bader, K. (2009). The impact of early-life maltreatment on dreams
of patients with insomnia. International Journal of Dream Research, 2, 18–26.
Schenck, C. H., Scott, R., Ettinger, M. G., & Mahowald, M. W. (1986). Chronic
behavioral disorders of human REM sleep: A new category of parasomnia.
Sleep, 9, 293–308.
Schredl, M. (1998a). Dream content in patients with narcolepsy: Preliminary find-
ings. Dreaming, 8, 103–107.
Schredl, M. (1998b). Träume und Schlafstörungen: Empirische Studie zur
Traumerinnerungshäufigkeit und zum Trauminhalt schlafgestörter
PatientInnen. Marburg: Tectum.
Schredl, M. (2001). Dream recall frequency and sleep quality of patients with rest-
less legs syndrome. European Journal of Neurology, 8, 185–189.
Schredl, M. (2009). Nightmare frequency in patients with primary insomnia.
International Journal of Dream Research, 2, 85–88.
Schredl, M. (2010). Do sleep disorders affect the dreaming process? Dream recall
and dream content in patients with sleep disorders. Sleep Medicine Clinics, 5(2),
193–202.
Schredl, M., & Engelhardt, H. (2001). Dreaming and psychopathology: Dream
recall and dream content of psychiatric inpatients. Sleep and Hypnosis, 3, 44–54.
Schredl, M., & Montasser, A. (1999). Dreaming and eating disorders. Sleep and
Hypnosis, 1, 225–231.
Schredl, M., & Schmitt, J. (2009). Dream recall frequency and nightmare fre-
quency in patients with sleep disordered breathing. Somnologie, 13, 12–17.
Schredl, M., Schäfer, G., Weber, B., & Heuser, I. (1998). Dreaming and insomnia:
Dream recall and dream content of patients with insomnia. Journal of Sleep
Research, 7, 191–198.
Schredl, M., Kraft-Schneider, B., Kröger, H., & Heuser, I. (1999). Dream content
of patients with sleep apnea. Somnologie, 3, 319–323.
DREAMS AND MENTAL DISORDERS 145
Schredl, M., Wittmann, L., Ciric, P., & Götz, S. (2003). Factors of home dream
recall: A structural equation model. Journal of Sleep Research, 12, 133–141.
Schredl, M., Schmitt, J., Hein, G., Schmoll, T., Eller, S., & Haaf, J. (2006).
Nightmares and oxygen desaturations: Is sleep apnea related to heightened
nightmare frequency? Sleep and Breathing, 10, 203–209.
Schredl, M., Hebel, M. E., Klütsch, R. C., & Liehe, L. J. (2009a). The role of
mood congruency memory effects in dream recall: A pilot study. Dreaming, 19,
113–118.
Schredl, M., Riemann, D., & Berger, M. (2009b). The effect of trimipramine on
dream recall and dream emotions in depressive outpatients. Psychiatry Research,
167, 279–286.
Schredl, M., Binder, R., Feldmann, S., Göder, R., Hoppe, J., Schmitt, J.,
Schweitzer, M., Specht, M., & Steinig, J. (2012). Dreaming in patients with
sleep disorders: A multicenter study. Somnologie, 16, 32–42.
Silber, M. H., St. Louis, E. K., & Boeve, B. F. (2017). Rapid eye movement sleep
parasomnias. In M. Kryger, T. Roth, & W. C. Dement (Eds.), Principles and
practice of sleep medicine (6th ed., pp. 993–1001). Philadelphia: Elsevier.
Skancke, J., Holsen, I., & Schredl, M. (2014). Continuity between waking life and
dreams of psychiatric patients: A review and discussion of the implications for
dream research. International Journal of Dream Research, 7, 39–53.
Strauch, I., & Meier, B. (1996). In search of dreams: Results of experimental dream
research. Albany: State University of New York Press.
Swart, M. L., van Schagen, A. M., Lancee, J., & van den Bout, J. (2013).
Prevalence of nightmare disorder in psychiatric outpatients. Psychotherapy and
Psychosomatics, 82(4), 267–268.
Tribl, G. G., Wetter, T. C., & Schredl, M. (2013). Dreaming under antidepres-
sants: A systematic review on evidence in depressive patients and healthy volun-
teers. Sleep Medicine Reviews, 17, 133–142.
Uguccioni, G., Golmard, J.-L., de Fontréaux, A. N., Leu-Semenescu, S., Brion,
A., & Arnulf, I. (2013). Fight or flight? Dream content during sleepwalking/
sleep terrors vs rapid eye movement sleep behavior disorder. Sleep Medicine,
14(5), 391–398.
Valipour, A., Lothaller, H., Rauscher, H., Zwick, H., Burghuber, O. C., & Lavie,
P. (2007). Gender-related differences in symptoms of patients with suspected
breathing disorders in sleep: A clinical population study using the sleep disor-
ders questionnaire. Sleep, 30, 306–313.
Valli, K., Frauscher, B., Gschliesser, V., Wolf, E., Falkenstetter, T., Schönwald,
S. V., Ehrmann, L., Zangerl, A., Marti, I., Boesch, S. M., Revonsuo, A., Poewe,
W., & Högl, B. (2012). Can observers link dream content to behaviours in
rapid eye movement sleep behaviour disorder? A cross-sectional experimental
pilot study. Journal of Sleep Research, 21, 21–29. [Link]
org/10.1111/j.1365-2869.2011.00938.x.
146 M. SCHREDL
Nightmares
7.1 Definitions
According to the International Classification of Sleep Disorders ICSD-3
(American Academy of Sleep Medicine 2014), nightmares are defined as
disturbing mental experiences that generally occur during REM sleep and
that often result in awakening. Most often the dream emotion is anxiety
but also other emotions like sadness, anger, guilt, and disgust can be the
prominent emotion of a nightmare (Robert and Zadra 2014). The most
common nightmare themes are being chased, falling, being paralyzed,
death of close persons, and being late (Schredl 2010a). Disturbing dreams
without causing an awakening are called “bad dreams”. As REM sleep is
more often found in the second half of the night, nightmares are also
reported to occur in the later part of the night. Upon awakening, the per-
son is fully awake, oriented about the surroundings, and able to give a full
account of the nightmare.
As most people have experienced nightmares at least occasionally in
their life span (Schredl et al. 2014), it is important to differentiate between
the general term nightmares and the nightmare disorder. In order to diag-
nose a nightmare disorder (ICD 10: F51.5), the person should report
clinically significant distress or impairment in social, occupational, or other
important areas of functioning due to the nightmares (American Academy
of Sleep Medicine 2014). In clinical practice, a cut-off of about one night-
mare per week or more often can be used as indication for the nightmare
disorder (Schredl 2013a). In children, the fear at sleep onset that
ightmares might occur during the night is another indicator for the dis-
n
tressing effect of nightmares (American Academy of Sleep Medicine
2014). The diagnostic criteria exclude patients with disorders which might
be causal for the nightmares like PTSD, major depression, or anxiety dis-
orders. It is, however, still unclear whether nightmares should be consid-
ered as symptom of these disorders or considered as co-morbid condition
(Schredl 2013a).
Nightmares are not the only phenomena occurring during the night that
are associated with anxiety; there are night terrors, post-traumatic re-
enactments, and nocturnal panic attacks. Night terrors occur most often
about one hour after sleep onset out of NREM sleep and are accompanied
with a massive autonomic arousal (loud vocalizations, dramatic increase in
heart rate) (American Academy of Sleep Medicine 2014). Usually, the
person is not fully awake and sleepwalking can occur after the night terror
attack. Night terrors can be differentiated from nightmares because the
sleeper often does not recall the night terror attack or at maximum a brief
scene or image like fire or a wall crushing down whereas nightmares are
easily recalled in detail. Post-traumatic re-enactments are replays of a trau-
matic event the person experienced in his/her waking life (Wittmann et al.
2007). These can occur during REM sleep but also during NREM sleep
and even in the waking state: then they are called “flashbacks”. Patients
suffering from PTSD often suffer from nightmares (American Psychiatric
Association 2013); about 50% of these nightmares are trauma-related
(more or less exact replay of the traumatic situation) whereas other night-
mares contain other distressing or terrifying topics (Wittmann et al. 2007).
Nocturnal panic attacks have their peak of experiencing anxiety and
panic after awakening, usually accompanied by death anxiety and somatic
symptoms like hyperventilation, paresthesias (numbness or tingling sensa-
tions), sweating and so on (American Psychiatric Association 2013),
whereas in the case of nightmares the anxiety decreases if the person is
fully alert (American Academy of Sleep Medicine 2014). It should be
noted, however, that nightmares can trigger nocturnal panic attacks in
patients with panic disorder (Schredl et al. 2001). Differentiating between
these four phenomena is very important from the clinical standpoint, as
effective therapeutic approaches are different.
NIGHTMARES 149
a
Frequent is defined as reporting one or more nightmares per week
152 M. SCHREDL
lying, and so on. The distribution depicted in Table 7.1 indicates that
there is a large variety of nightmare topics; this distribution is roughly
comparable between the total sample (including many persons with infre-
quent nightmares) and the persons with frequent nightmares.
Unfortunately, content analytic studies in patients with a diagnosed night-
mare disorder are still lacking.
Factors
Genetics
Trait factors (neuroticism, “thin boundaries”)
Early adverse events
Psychopathology
Stress
Trauma
Side effects of medication
NIGHTMARES 153
7.7 Therapy
Nightmares, more specific, the nightmare disorder, are underdiagnosed
and undertreated (Nadorff et al. 2015; Schredl 2010b). There are several
plausible reasons for that. First, even in sleep centers the physician often
does not ask explicitly about nightmares as most of the patients are seeking
help for symptoms of insomnia, restless legs syndrome, or sleep apnea; if
specifically asked the prevalence rate of nightmare disorder was 16.3%
NIGHTMARES 155
Step 1: Confrontation
Recording or drawing the dream
Step 2: Coping with the situation in the nightmare
Construct a new dream ending or add something to the drawing that reduces the
anxiety
Step 3: Training of the new coping strategy
About 5–10 minutes per day over a two-week period
156 M. SCHREDL
ior), the therapist should ask whether there are additional options to cope
with the situation. The new ending of the dream does not have to be
realistic but most psychologists do not recommend an increase of vio-
lence, for example, fighting the monster. This is based on concepts that
dream characters might represent aspects of the dreamer’s personality
(Faraday 1990), for example, a dream monster might reflect the dreamer’s
fear of being aggressive, and, thus, communication with threating dream
characters is encouraged. The new “dream” should be written down
(Krakow and Zadra 2010). Children are asked to complement the dream
drawing with the elements that she/he had come up with and that are
helpful (St-Onge et al. 2009). By imagining this new approach to cope
with the nightmare situation once a day for 5–10 minutes for two weeks,
subsequent dreams will be affected by this training (Germain et al. 2004).
Several meta-analyses (Augedal et al. 2013; Casement and Swanson
2012; Hansen et al. 2013; Seda et al. 2015) of randomized controlled
trials indicate that Imagery Rehearsal Therapy is very effective in reduc-
ing nightmare frequency. This has been shown for adult idiopathic night-
mare sufferers (Krakow et al. 1995), for children with nightmares
(St-Onge et al. 2009), for sexually assaulted women as well as other
patients with PTSD (Seda et al. 2015), and for patients with mental dis-
orders, for example, major depression, and co-morbid nightmare disor-
der (Thünker and Pietrowsky 2012; van Schagen et al. 2016). One large
study in women with PTSD, however, indicated that Imagery Rehearsal
Therapy alone is not sufficient for treating severely traumatized persons,
about 40% of this group dropped out (Krakow et al. 2001). Systematic
studies applying Imagery Rehearsal Therapy as an add-on to standard
treatment of PTSD have not been carried out yet. Interestingly, most
studies indicate that the reduction of nightmares also improves other
clinical symptoms of the patients like depressive mood, daytime function-
ing, and sleep quality (Augedal et al. 2013). In addition, the effectiveness
of self-help programs (Lancee et al. 2010) and online programs
(Gieselmann et al. 2017) have been demonstrated. One study (Kunze
et al. 2017) has tested whether single components of the Imagery
Rehearsal Therapy like exposure or rescripting might be sufficient to
reduce nightmares. In addition to Imagery Rehearsal Therapy, desensiti-
zation in sensu and exposure in sensu have been effective (Augedal et al.
2013), also lucid dreaming (Harb et al. 2016).
NIGHTMARES 157
References
American Academy of Sleep Medicine. (2014). The international classification of
sleep disorders (ICSD-3). Darien: AASM.
American Psychiatric Association. (2013). Diagnostic and statistical manual of
mental disorders: DSM-5. Washington, DC: American Psychiatric Association.
Augedal, A. W., Hansen, K. S., Kronhaug, C. R., Harvey, A. G., & Pallesen, S.
(2013). Randomized controlled trials of psychological and pharmacological
treatments for nightmares: A meta-analysis. Sleep Medicine Reviews, 7, 143–152.
Belicki, K. (1992a). Nightmare frequency versus nightmare distress: Relation to
psychopathology and cognitive style. Journal of Abnormal Psychology, 101,
592–597.
Belicki, K. (1992b). The relationship of nightmare frequency to nightmare suffer-
ing with implications for treatment and research. Dreaming, 2, 143–148.
Bixler, E. O., Kales, A., Soldatos, C. R., Kales, J. D., & Healey, S. (1979).
Prevalence of sleep disorders in the Los Angeles metropolitan area. American
Journal of Psychiatry, 136, 1257–1262.
Boerner, J. (1855). Das Alpdrücken: Seine Begründung und Verhütung. Würzburg:
Carl Joseph Becker.
Carr, M., & Nielsen, T. (2017). A novel differential susceptibility framework for
the study of nightmares: Evidence for trait sensory processing sensitivity.
Clinical Psychology Review, 58, 86–96.
Casement, M. D., & Swanson, L. M. (2012). A meta-analysis of imagery rehearsal
for post-trauma nightmares: Effects on nightmare frequency, sleep quality, and
posttraumatic stress. Clinical Psychology Review, 32(6), 566–574.
Cuddy, M. A., & Belicki, K. (1992). Nightmare frequency and related sleep dis-
turbance as indicators of a history of sexual abuse. Dreaming, 2, 15–22.
Faraday, A. (1990). The dream game. New York: Harper & Row.
Germain, A., Krakow, B., Faucher, B., Zadra, A. L., Nielsen, T. A., Hollifield, M.,
Warner, T. D., & Koss, M. (2004). Increased mastery elements associated with
imagery rehearsal treatment for nightmares in sexual assault survivors with
PTSD. Dreaming, 14, 195–206.
Gieselmann, A., Böckermann, M., Sorbi, M., & Pietrowsky, R. (2017). The effects
of an internet-based imagery rehearsal intervention: A randomized controlled
trial. Psychotherapy and Psychosomatics, 86(4), 231–240.
Hansen, K., Höfling, V., Kröner-Borowik, T., Stangier, U., & Steil, R. (2013).
Efficacy of psychological interventions aiming to reduce chronic nightmares: A
meta-analysis. Clinical Psychology Review, 33(1), 146–155.
Harb, G. C., Brownlow, J. A., & Ross, R. J. (2016). Posttraumatic nightmares and
imagery rehearsal: The possible role of lucid dreaming. Dreaming, 26(3),
238–249.
Hartmann, E. (1984). The nightmare: The psychology and biology of terrifying
dreams. New York: Basic Books.
158 M. SCHREDL
Michels, F., Schilling, C., Rausch, F., Eifler, S., Zink, M., Meyer-Lindenberg, A.,
& Schredl, M. (2014). Nightmare frequency in schizophrenic patients, healthy
relatives of schizophrenic patients, patients at high risk states for psychosis, and
healthy controls. International Journal of Dream Research, 5, 9–13.
Nadorff, M. R., Nadorff, D. K., & Germain, A. (2015). Nightmares: Under-
reported, undetected, and therefore untreated. Journal of Clinical Sleep
Medicine, 11(7), 747–750.
Nielsen, T. A. (2017). The stress acceleration hypothesis of nightmares. Frontiers
in Neurology, 8, 201. [Link]
Nielsen, T. A., & Powell, R. A. (2015). Dreams of the rarebit fiend: Food and diet
as instigators of bizarre and disturbing dreams. Frontiers in Psychology, 6.
[Link]
Pagel, J. F., & Helfter, P. (2003). Drug induced nightmares – An etiology based
review. Human Psychopharmacology, 18, 59–67.
Paul, F., Schredl, M., & Alpers, G. W. (2015). Nightmares affect the experience of
sleep quality but not sleep architecture: An ambulatory polysomnographic
study. Borderline Personality Disorder and Emotion Dysregulation, 2(3), 1–9.
Robert, G., & Zadra, A. L. (2008). Measuring nightmare and bad dream fre-
quency: Impact of retrospective and prospective instruments. Journal of Sleep
Research, 17, 132–139.
Robert, G., & Zadra, A. L. (2014). Thematic and content analysis of idiopathic
nightmares and bad dreams. Sleep: Journal of Sleep and Sleep Disorders Research,
37(2), 409–417.
Sandman, N., Valli, K., Kronholm, E., Ollila, H. M., Revonsuo, A., Laatikainen,
T., & Paunio, T. (2013). Nightmares: Prevalence among the Finnish general
adult population and war veterans during 1972–2007. Sleep, 36, 1041–1050.
Schredl, M. (2003a). Continuity between waking and dreaming: A proposal for a
mathematical model. Sleep and Hypnosis, 5, 38–52.
Schredl, M. (2003b). Effects of state and trait factors on nightmare frequency.
European Archives of Psychiatry and Clinical Neuroscience, 253, 241–247.
Schredl, M. (2010a). Nightmare frequency and nightmare topics in a representa-
tive German sample. European Archives of Psychiatry and Clinical Neuroscience,
260, 565–570.
Schredl, M. (2010b). Nightmares: An under-diagnosed and undertreated condi-
tion? Commentary on Li et al. prevalence and correlates of frequent night-
mares: A community-based 2-phase study. Sleep, 33, 733–734.
Schredl, M. (2013a). Nightmare disorder. In C. Kushida (Ed.), The encyclopedia of
sleep (Vol. 4, pp. 219–224). Waltham: Academic.
Schredl, M. (2013b). Nightmare frequency in a representative German sample.
International Journal of Dream Research, 6, 119–122.
Schredl, M. (2013c). Seeking professional help for nightmares: A representative
study. European Journal of Psychiatry, 27, 259–264.
160 M. SCHREDL
St-Onge, M., Mercier, P., & De Koninck, J. (2009). Imagery rehearsal therapy for
frequent nightmares in children. Behavioral Sleep Medicine, 7, 81–98.
Stumbrys, T., Erlacher, D., & Schredl, M. (2013). Reliability and stability of lucid
dream and nightmare frequency scales. International Journal of Dream
Research, 6, 123–126.
Swart, M. L., van Schagen, A. M., Lancee, J., & van den Bout, J. (2013).
Prevalence of nightmare disorder in psychiatric outpatients. Psychotherapy and
Psychosomatics, 82(4), 267–268.
Thünker, J., & Pietrowsky, R. (2012). Effectiveness of a manualized imagery
rehearsal therapy for patients suffering from nightmare disorders with and
without a comorbidity of depression or PTSD. Behaviour Research and Therapy,
50(9), 558–564.
Thünker, J., Norpoth, M., von Aspern, M., Özcan, T., & Pietrowsky, R. (2014).
Nightmares: Knowledge and attitudes in health care providers and nightmare
sufferers. Journal of Public Health and Epidemiology, 6, 223–228.
Tribl, G. G., Wetter, T. C., & Schredl, M. (2013). Dreaming under antidepres-
sants: A systematic review on evidence in depressive patients and healthy volun-
teers. Sleep Medicine Reviews, 17, 133–142.
van Schagen, A. M., Lancee, J., Spoormaker, V. I., & van den Bout, J. (2016).
Long-term treatment effects of imagery rehearsal therapy for nightmares in a
population with diverse psychiatric disorders. International Journal of Dream
Research, 9, 67–70.
van Schagen, A. M., Lancee, J., Swart, M., Spoormaker, V., & van den Bout,
J. (2017). Nightmare disorder, psychopathology levels, and coping in a diverse
psychiatric sample. Journal of Clinical Psychology, 73(1), 65–75.
Wittmann, L., Schredl, M., & Kramer, M. (2007). The role of dreaming in post-
traumatic stress disorder. Psychotherapy and Psychosomatics, 76, 25–39.
Wood, J. M., & Bootzin, R. R. (1990). The prevalence of nightmares and their
independence from anxiety. Journal of Abnormal Psychology, 99, 64–68.
Zadra, A. L., & Donderi, D. C. (2000). Nightmares and bad dreams: Their preva-
lence and relationship to well-being. Journal of Abnormal Psychology, 109,
273–281.
Zunker, M., Althoff, H. K., Apel, J., Lässig, H. S., Schültke, L., & Schredl, M.
(2015). Comparing questionnaire and diary measures for eliciting nightmare
frequency. International Journal of Dream Research, 8, 129–134.
CHAPTER 8
Lucid Dreaming
8.1 Definitions
A scale measuring lucid dreaming frequency (Schredl and Erlacher 2004)
provides the following definition: “In a lucid dream, one is, while dream-
ing, aware of the fact that one is dreaming. It is possible to wake up delib-
erately, or to control the dream action, or to observe passively the course
of the dream with this awareness.” The basic criterion for a lucid dream is
the awareness of the dreaming state (LaBerge 1985), whereas the ability
to control the dream action and remembering waking life are possible
additional features of lucid dreams (Gackenbach and LaBerge 1986). In
non-selected student sample only 0.3–1.4% of diary dream reports are
lucid (Schredl and Noveski 2017; Zadra et al. 1992). However, results are
dramatically different if the dreamer is presented with a self-rating scale,
for example “I was aware that I was dreaming” (0 = not at all, 1 = just a
little, 2 = moderately, 3 = pretty much, 4 = very much); the percentage of
dream reports with some kind of lucidity was 49.1% (Dyck et al. 2017). As
questionnaires like the LuCiD (Voss et al. 2013) and the TDQ (Stumbrys
et al. 2013b) have been used in experimental studies, the question arises
what the differences between a full-blown lucid dream with explicitly
mentioned knowledge that one is dreaming and dreams with a little bit
of lucidity are. One cannot rule out that it might be a methodological
issue, that is, persons participating in a lucid dreaming study might state
“a little lucidity” to satisfy the experimenter but did not experience lucid-
ity. Further studies, preferably of a qualitative nature, are necessary.
Another dream type that is not fully lucid are so-called pre-lucid dreams:
“The subjects adopt a critical attitude towards what he is experiencing,
even to the point of asking himself ‘Am I dreaming?’ but without realizing
that he is in fact doing so” (p. 23; Green 1968). A dream example of the
author might help to illustrate this dream type. He was flying in a mall and
was wondering why he could fly in the waking state because flying is only
possible in dreaming, that is, he thought he was awake and noticed the
bizarre element in the dream but did not realize that he was dreaming.
The frequency of pre-lucid dreams is comparable to those of lucid dreams
(0.6–1.0%) (Schredl and Noveski 2017; Zadra et al. 1992) and, thus, the
occurrence of pre-lucid dreams cannot explain the high percentage of
lucid dreaming using self-rating scales.
Cognitive techniques
Dream-Initiated Lucid Dream, for example, Mnemonic Induction of Lucid Dreams,
Reality Checks
Wake-Initiated Lucid Dream, for example, counting while falling asleep
External stimulation (light, sound, tactile stimuli, transcranial direct or alternate current
stimulation)
Other approaches (Wake-up-Back-to-Bed technique, drugs)
166 M. SCHREDL
then awakened from REM sleep in order to obtain a “fresh” dream. During
the next hour, the participant is instructed to practice MILD (see above)
for this dream. Then she/he can continue sleeping for an additional two or
three hours. The success rate for dreaming lucidly in this second sleep
period was about 50%, even in non-experienced lucid dreamers (Stumbrys
and Erlacher 2014). For experienced lucid dreamers it was even higher:
60% (9 out of 15) (Schädlich et al. 2017). However, the effect in the home
setting is much smaller (Aspy et al. 2017) or even not present (Dyck et al.
2017); the main problem is that the awakening might not be out of REM,
that is, the MILD technique cannot be applied to a “fresh” dream and it
seems difficult to focus on the task for one hour—if not constantly moti-
vated by the experimenter who is present in the sleep lab setting.
Stumbrys et al. (2012) evaluated the induction studies using a rating
system for methodological quality; the results were not encouraging as the
quality of most studies was relatively low. On the other hand, this is
encouraging for future research as many questions are still unanswered,
for example, whether everyone can learn lucid dreaming and which tech-
nique is best for a specific dreamer.
References
American Academy of Sleep Medicine. (2007). The AASM manual for the scoring
of sleep and associated events: Rules, terminology, and technical specifications.
Westchester: American Academy of Sleep Medicine.
Appel, K., & Pipa, G. (2017). Auditory evoked potentials in lucid dreams: A dis-
sertation summary. International Journal of Dream Research, 10(1), 98–100.
Aspy, D. J. (2016). Is dream recall underestimated by retrospective measures and
enhanced by keeping a logbook? An empirical investigation. Consciousness and
Cognition, 42, 181–203.
Aspy, D. J., Delfabbro, P., Proeve, M., & Mohr, P. (2017). Reality testing and the
mnemonic induction of lucid dreams: Findings from the national Australian
lucid dream induction study. Dreaming, 27(3), 206–231.
Dresler, M., Koch, S. P., Wehrle, R., Spoormaker, V. I., Holsboer, F., Steiger, A.,
Sämann, P. G., Obrig, H., & Czisch, M. (2011). Dreamed movement elicits
activation in the sensorimotor cortex. Current Biology, 21, 1833–1837.
Dresler, M., Wehrle, R., Spoormaker, V. I., Koch, S. P., Holsboer, F., Steiger, A.,
Obrig, H., Samann, P. G., & Czisch, M. (2012). Neural correlates of dream
LUCID DREAMING 171
lucidity obtained from contrasting lucid versus non-lucid REM sleep: A com-
bined EEG/fMRI case study. Sleep, 35, 1017–1020.
Dyck, S., Schredl, M., & Kühnel, A. (2017). Lucid dream induction using three
different cognitive methods. International Journal of Dream Research, 10(2),
151–156.
Erlacher, D., & Schredl, M. (2010). Practicing a motor task in a lucid dream
enhances subsequent performance: A pilot study. Sport Psychologist, 24,
157–167.
Erlacher, D., Schredl, M., Watanabe, T., Yamana, J., & Gantzert, F. (2008). The
incidence of lucid dreaming within a Japanese university student sample.
International Journal of Dream Research, 1, 39–43.
Erlacher, D., Schädlich, M., Stumbrys, T., & Schredl, M. (2014). Time for actions
in lucid dreams: Effects of task modality, length, and complexity. Frontiers in
Psychology, 4. [Link]
Gackenbach, J., & LaBerge, S. (1986). An overview of lucid dreaming. In
A. Sheikh (Ed.), International review of mental imagery (Vol. 2, pp. 57–89).
New York: Human Sciences Press.
Green, C. (1968). Lucid dreams. London: Hamish Hamilton.
Hearne, K. M. T. (1978). Lucid dreams: An electrophysiological and psychological
study. Doctoral dissertation, University of Liverpool.
Hess, G., Schredl, M., & Goritz, A. S. (2016). Lucid dreaming frequency and the
Big Five personality factors. Imagination, Cognition and Personality, 36(3),
240–253.
Kellogg, E. W. (2017). The outer limits of lucid dreaming. International Journal
of Dream Research, 10(Suppl 1), S47–S48.
Kern, S., Appel, K., Schredl, M., & Pipa, G. (2017). No effect of α-GPC on lucid
dream induction or dream content. Somnologie, 21(3), 180–186.
LaBerge, S. P. (1980). Lucid dreaming: An exploratory study of consciousness dur-
ing sleep. Doctoral dissertation, Stanford University.
LaBerge, S. P. (1985). Lucid dreaming. Los Angeles: Jeremy P. Tarcher.
LaBerge, S. P., & Levitan, L. (1995). Validity established of dreamlight cues for
eliciting lucid dreaming. Dreaming, 5, 159–168.
Moers-Messmer, H. V. (1939). Träume mit der gleichzeitigen Erkenntnis des
Traumzustandes. Archiv für die Gesamte Psychologie, 102, 291–318.
Paul, F., Schädlich, M., & Erlacher, D. (2014). Lucid dream induction by visual
and tactile stimulation: An exploratory sleep laboratory study. International
Journal of Dream Research, 7(1), 61–66.
Saint-Denys, H. de (1982). Dreams and how to guide them (Original: 1867).
London: Duckworth.
Saunders, D. T., Roe, C. A., Smith, G., & Clegg, H. (2016). Lucid dreaming
incidence: A quality effects meta-analysis of 50 years of research. Consciousness
and Cognition, 43, 197–215.
172 M. SCHREDL
Saunders, D. T., Clegg, H., Roe, C. A., & Smith, G. D. (2017). Exploring the role
of need for cognition, field independence and locus of control on the incidence
of lucid dreams during a 12-week induction study. Dreaming, 27(1), 68–86.
Schädlich, M., & Erlacher, D. (2012). Applications of lucid dreams: An online
study. International Journal of Dream Research, 5, 134–138.
Schädlich, M., Erlacher, D., & Schredl, M. (2017). Improvement of darts perfor-
mance following lucid dream practice depends on the number of distractions
while rehearsing within the dream – A sleep laboratory pilot study. Journal of
Sports Sciences, 35(23), 2365–2372.
Schredl, M., & Erlacher, D. (2004). Lucid dreaming frequency and personality.
Personality and Individual Differences, 37, 1463–1473.
Schredl, M., & Erlacher, D. (2011). Frequency of lucid dreaming in a representa-
tive German sample. Perceptual and Motor Skills, 111, 60–64.
Schredl, M., & Noveski, A. (2017). Lucid dreaming: A diary study. Imagination,
Cognition and Personality. [Link]
Schredl, M., Henley-Einion, J., & Blagrove, M. (2016). Lucid dreaming and per-
sonality in children/adolescents and adults: The UK library study. International
Journal of Dream Research, 9, 75–78.
Siegel, J. M. (2017). Rapid eye movement sleep. In M. Kryger, T. Roth, & W. C.
Dement (Eds.), Principles and practice of sleep medicine (6th ed., pp. 78–95).
Philadelphia: Elsevier.
Sparrow, G. S., Carlson, R., & Hurd, R. (2016). Assessing the perceived differ-
ences in post-Galantamine lucid dreams vs. Non-Galantamine lucid dreams.
International Journal of Dream Research, 9, 71–74.
Spoormaker, V. I., & Van den Bout, J. (2006). Lucid dreaming treatment for
nightmares: A pilot study. Psychotherapy and Psychosomatics, 75, 389–394.
Strelen, J. O. (2005). Akustisch evozierte Potentiale bei luziden Träumen – eine
Untersuchung über diskriminierendes Wahrnehmen und selektives Beantworten
von Tönen in REM-Schlaf, Dissertation, Mainz.
Stumbrys, T., & Erlacher, D. (2014). The science of lucid dream induction. In
R. Hurd & K. Bulkeley (Eds.), Lucid dreaming: New perspectives on conscious-
ness in sleep, Science, psychology, and education (Vol. 1, pp. 77–102). Santa
Barbara: Praeger.
Stumbrys, T., & Erlacher, D. (2016). Applications of lucid dreams and their effects
on the mood upon awakening. International Journal of Dream Research, 9(2),
146–150.
Stumbrys, T., Erlacher, D., Schädlich, M., & Schredl, M. (2012). Induction of
lucid dreams: A systematic review of evidence. Consciousness and Cognition,
21(3), 1456–1475.
Stumbrys, T., Erlacher, D., & Schredl, M. (2013a). Reliability and stability of
lucid dream and nightmare frequency scales. International Journal of Dream
Research, 6, 123–126.
LUCID DREAMING 173
Stumbrys, T., Erlacher, D., & Schredl, M. (2013b). Testing the involvement of
the prefrontal cortex in lucid dreaming: A tDCS study. Consciousness and
Cognition, 22(4), 1214–1222.
Stumbrys, T., Erlacher, D., Johnson, M., & Schredl, M. (2014). The phenome-
nology of lucid dreaming: An online survey. American Journal of Psychology,
127(2), 191–204.
Stumbrys, T., Erlacher, D., & Malinowski, P. (2015). Meta-awareness during day
and night: The relationship between mindfulness and lucid dreaming.
Imagination, Cognition and Personality, 34(4), 415–433.
Stumbrys, T., Erlacher, D., & Schredl, M. (2016). Effectiveness of motor practice
in lucid dreams: A comparison with physical and mental practice. Journal of
Sports Sciences, 34(1), 27–34.
Van Eeden, F. (1913). A study of dreams. Proceedings of the Society for Psychical
Research, 26, 431–461.
Voss, U., Holzmann, R., Tuin, I., & Hobson, J. A. (2009). Lucid dreaming: A
state of consciousness with features of both waking and non-lucid dreaming.
Sleep, 32, 1191–1200.
Voss, U., Schemelleh-Engel, K., Windt, J. M., Frenzel, C., & Hobson, A. (2013).
Measuring consciousness in dreams: The lucidity and consciousness in dreams
scale. Consciousness and Cognition, 22, 8–21.
Voss, U., Holzmann, R., Hobson, A., Paulus, W., Koppehele-Gossel, J., Klimke,
A., & Nitsche, M. A. (2014). Induction of self awareness in dreams through
frontal low current stimulation of gamma activity. Nature Neuroscience, 17(6),
810–812.
Wangyal Rinpoche, T. (1998). The Tibetan yogas of dream and sleep. Ithaca: Snow
Lion.
Watson, D. (2001). Dissociations of the night: Individual differences in sleep-
related experiences and their relation to dissociation and schizotypy. Journal of
Abnormal Psychology, 110, 526–535.
Zadra, A. L., Donderi, D. C., & Pihl, R. O. (1992). Efficacy of lucid dream induc-
tion for lucid and non-lucid dreamers. Dreaming, 2, 85–97.
Zunker, M., Althoff, H. K., Apel, J., Lässig, H. S., Schültke, L., & Schredl, M.
(2015). Comparing questionnaire and diary measures for eliciting nightmare
frequency. International Journal of Dream Research, 8, 129–134.
CHAPTER 9
Functions of Dreaming
Before reviewing the major theories regarding dream function(s) that have
been published, it is important to explicate the problems that are inherent
in empirical investigations of dream function. The publication of Dement
(1960) entitled “The effect of dream deprivation” is very illustrative for the
first topic that should be kept in mind. In this study seven young men spent
three to seven nights in the sleep laboratory and were awakened if the poly-
somnographic recording indicated the presence of REM sleep. The num-
ber of awakenings per night had to be increased to 30 because there is an
REM rebound effect, that is, in normal sleep the first REM period occurs
after about 90–100 minutes after sleep onset but depriving REM sleep can
shorten this latency considerably. The normal amount of REM sleep (typi-
cally 20% of the total sleep time) was reduced by 75%, that is, it was not
possible to suppress all REM sleep. In order to control for the effect of the
awakenings on waking life, the participants spent more nights in the sleep
lab and were awakened from NREM sleep as often as in the first set of
nights (REM deprivation). REM sleep was only minimally reduced in this
condition. As participants reported more negative effects of the REM
deprivation part, psychological disturbances such as anxiety, irritability, and
difficulty in concentrating, Dement (1960) concluded that it was the effect
of dream deprivation. First, subsequent studies indicated that this negative
effect of REM deprivation on psychological functioning was explained by
the necessary very frequent sleep disruption and was not REM sleep spe-
cific (Ellman et al. 1978), that is, the findings of Dement (1960) might be
explained by a serial effect as the condition with the NREM awakenings
were always after the REM deprivation condition. Did Dement (1960)
deprive dreaming? Yes and no; he reduced the time of REM dreaming but
did not account for NREM dreaming. Can Dement (1960) differentiate
between the effect of reduced REM sleep and the reduced time of REM
dreaming? No, this is the major problem for these type of experiments:
there is no experimental procedure to carry out an isolated dream depriva-
tion without affecting the sleep, that is, total dream deprivation would
result in total sleep deprivation, and that total sleep deprivation affects the
person in a marked way is obvious and empirically demonstrated (e.g.,
Labelle et al. 2015). So, it is crucial to differentiate between the physiologi-
cal level (sleep in general and especially REM sleep) and the psychological
level (dreaming). The function(s) of REM sleep cannot be equated with
the function(s) of dreaming. In addition, dreaming as subjective experi-
ences, which are recallable after awakening, does not reflect the total brain
activity during REM sleep or other sleep stages, for example, REM sleep
plays a role in memory consolidation (Walker 2005), but this might happen
on a cellular or systems level without any consciousness involved.
The second problem is a methodological one, namely, how can an exper-
iment be conducted to support the idea that dreams are beneficial for sub-
sequent waking life. Rosalind Cartwright, for example, found that divorced
women who dreamed about their ex-husbands were more psychologically
adapted one year after the divorce than women who dreamed about other
topics (Cartwright 1996). One possible conclusion is that working through
the divorce issue within the dream serves an adaptive function. But equally
plausible is the alternative explanation: the women who reported the ex-
husband dreams began to think about their dreams and, therefore, were
able to cope better with the stressful divorce. The problem—and it seems
unsolvable— is that one cannot differentiate between the effect of dreaming
itself and the effect of the recalled, reported dream which is processed by the
waking mind as unremembered dreams are not accessible.
Despite these problems, a variety of hypotheses regarding dream func-
tion have been proposed (see Table 9.1).
Ray Meddis (1977) and Owen Flanagan (2000) put forward the idea
that dreams are a pure epiphenomenon and did not have any additional
functions to the well-documented functions of sleep and REM sleep, for
example, memory consolidation; that is, human consciousness has a func-
tion in waking (problem solving etc.) and nature did not bother to turn
off this function during sleep. This viewpoint is compatible with the
activation-synthesis hypothesis that postulates that dreams reflect the
FUNCTIONS OF DREAMING 177
Dreams as epiphenomenon
Guardian of sleep
Compensation
Iterative programming
Reverse learning hypothesis
Mastery hypothesis
Mood regulation
Systematic desensitization
Threat simulation theory
Protoconsciousness theory
Social simulation theory
Sleep-dependent memory consolidation
out in Chap. 4 there are parallels between basic problem solving and
dreaming. Dreams, for example, combine old information of the dream-
er’s past with current waking-life topics and play through different sce-
narios in order to evaluate the possible outcomes. The creative aspect of
dreaming can be seen as a kind of brainstorming to produce new solutions
for the problem (Barrett 2007). The function that dreams regulate mood
was proposed by Milton Kramer (2007) based on his findings that more
extreme emotions in the evening and during the night are evened out in
the morning. The extreme low muscle tone during REM sleep was a key
element for the theory of Perlis and Nielsen (1993). They hypothesized
that REM sleep presents the ideal condition for extinction, that is, experi-
encing anxiety while deeply relaxed helps to unlearn the anxiety, a com-
mon technique applied in cognitive-behavioral therapy. The threat
simulation theory (Revonsuo 2000) postulates that simulation of threats
during dreaming enhances survival and reproductive success because
humans will avoid dangerous situations and places (in the ancestral envi-
ronment thousands of years ago) by rehearsing this information during
sleep. A very recent theory was formulated by Allan Hobson (2009) who
conceptualized the dream as a level of consciousness where the mind can
prepare itself for future tasks that are crucial for living successfully in the
waking world. As mentioned in Chap. 4, social interactions are an impor-
tant topic in dreams much more than academics. As social skills were help-
ful in surviving and producing offspring for our ancestors the social
simulation theory proposes that rehearsing social skills might be a possible
function of dreaming (Revonsuo et al. 2015).
Based on the well-documented findings that sleep contributes to mem-
ory consolidation (Diekelmann et al. 2009), the first question that comes
to the mind is whether dreaming is reflecting the processes involved in
sleep-dependent memory consolidation (Graveline and Wamsley 2015).
In a nap study using a maze learning paradigm, performance gains were
higher if task-related dreams were reported (Wamsley et al. 2010).
However, an overnight study (Schredl and Erlacher 2010) using mirror
tracing as a procedural learning task did not show any relation between
task-related dreams and next day performance gain in the participants.
Keeping in mind that memory consolidation involves processes on a cel-
lular level (long-term potentiation) or on a network level, the question is
whether dreaming is functionally connected with sleep-dependent mem-
ory consolidation or just reflects these processes is not yet answered.
FUNCTIONS OF DREAMING 179
References
Barrett, D. (2007). An evolutionary theory of dreams and problem-solving. In
D. Barrett & P. McNamara (Eds.), The new science of dreaming – Volume 3:
Cultural and theoretical perspectives (pp. 133–153). Westport: Praeger.
Cartwright, R. D. (1996). Dreams and the adaption to divorce. In D. Barrett
(Ed.), Trauma and dreams (pp. 179–185, 262–163). Cambridge, MA: Harvard
University Press.
Crick, F., & Mitchison, G. (1983). The function of dream sleep. Nature, 304,
111–114.
Dement, W. C. (1960). The effect of dream deprivation. Science, 131, 1705–1707.
Diekelmann, S., Wilhelm, I., & Born, J. (2009). The whats and whens of sleep-
dependent memory consolidation. Sleep Medicine Reviews, 13, 309–321.
Ellman, S. J., Spielman, A. J., Luck, D., Steiner, S. S., & Halperin, R. (1978).
REM deprivation: A review. In A. M. Arkin, J. S. Antrobus, & S. J. Ellman
(Eds.), The mind in sleep: Psychology and psychophysiology (pp. 419–457).
Hillsdale: Lawrence Erlbaum.
Erlacher, D., & Schredl, M. (2010). Practicing a motor task in a lucid dream
enhances subsequent performance: A pilot study. Sport Psychologist, 24,
157–167.
Flanagan, O. (2000). Dreaming souls: Sleep, dreams, and the evolution of the con-
scious mind. Oxford: Oxford University Press.
180 M. SCHREDL
Stumbrys, T., Erlacher, D., & Schredl, M. (2016). Effectiveness of motor practice
in lucid dreams: A comparison with physical and mental practice. Journal of
Sports Sciences, 34(1), 27–34.
Walker, M. P. (2005). A refined model of sleep and the time course of memory
formation. Behavioral and Brain Sciences, 28, 51–64.
Wamsley, E. J., Tucker, M., Payne, J. D., Benavides, J. A., & Stickgold, R. (2010).
Dreaming of a learning task is associated with enhanced sleep-dependent mem-
ory consolidation. Current Biology, 20, 850–855.
Wright, J., & Koulack, D. (1987). Dreams and contemporary stress: A disruption-
avoidance-adaptation model. Sleep, 10, 172–179.
References
Armitage, R., Rochlen, A., Fitch, T., Trivedi, M., & Rush, A. J. (1995). Dream
recall and major depression: A preliminary report. Dreaming, 5, 189–198.
Arnulf, I., Grosliere, L., Le Corvec, T., Golmard, J.-L., Lascols, O., & Duguet, A.
(2014). Will students pass a competitive exam that they failed in their dreams?
Consciousness and Cognition, 29, 36–47.
Aserinsky, E., & Kleitman, N. (1953). Regularly occurring periods of eye motility
and concomitant phenomena during sleep. Science, 118, 273–274.
Aserinsky, E., Lynch, J. A., Mack, M. E., Tzankoff, S. P., & Hurn, E. (1985).
Comparison of eye motion in wakefulness and REM sleep. Psychophysiology, 22,
1–10.
Aspy, D. J., Delfabbro, P., & Proeve, M. (2015). Is dream recall underestimated
by retrospective measures and enhanced by keeping a logbook? A review.
Consciousness and Cognition, 33, 364–374.
Aspy, D. J. (2016). Is dream recall underestimated by retrospective measures and
enhanced by keeping a logbook? An empirical investigation. Consciousness and
Cognition, 42, 181–203.
Aspy, D. J., Delfabbro, P., Proeve, M., & Mohr, P. (2017). Reality testing and the
mnemonic induction of lucid dreams: Findings from the national Australian
lucid dream induction study. Dreaming, 27(3), 206–231.
Augedal, A. W., Hansen, K. S., Kronhaug, C. R., Harvey, A. G., & Pallesen, S.
(2013). Randomized controlled trials of psychological and pharmacological
treatments for nightmares: A meta-analysis. Sleep Medicine Reviews, 7, 143–152.
Aumann, C., Lahl, O., & Pietrowsky, R. (2012). Relationship between dream
structure, boundary structure and the Big Five personality dimensions.
Dreaming, 22(2), 124–135.
Baekeland, F., Resch, R., & Katz, D. (1968). Presleep mentation and dream
reports: I. Cognitive style, contiguity to sleep and time of the night. Archives of
General Psychiatry, 19, 300–311.
Bandalos, D. L. (2018). Measurement theory and applications for the social sciences.
New York: Guilford Publications.
Barrett, D. (2001). The committee of sleep: How artists, scientists, and athletes use
dreams for creative problem-solving – And how you can too. New York: Crown.
Barrett, D. (2007). An evolutionary theory of dreams and problem-solving. In
D. Barrett & P. McNamara (Eds.), The new science of dreaming – Volume 3:
Cultural and theoretical perspectives (pp. 133–153). Westport: Praeger.
Beauchemin, K. M., & Hays, P. (1995). Prevailing mood, mood changes and
dreams in bipolar disorder. Journal of Affective Disorders, 35, 41–49.
Beauchemin, K. M., & Hays, P. (1996). Dreaming away depression: The role of
REM sleep and dreaming in affective disorders. Journal of Affective Disorders,
41, 125–133.
Beaulieu-Prevost, D., & Zadra, A. L. (2005). Dream recall frequency and attitude
towards dreams: A reinterpretation of the relation. Personality and Individual
Differences, 38, 919–927.
REFERENCES
185
Blagrove, M., Henley-Einion, J., Barnett, A., Edwards, D., & Seage, C. H.
(2011b). A replication of the 5–7 day dream-lag effect with comparison of
dreams to future events as control for baseline matching. Consciousness and
Cognition, 20(2), 384–391.
Boerner, J. (1855). Das Alpdrücken: Seine Begründung und Verhütung. Würzburg:
Carl Joseph Becker.
Bokert, E. G. (1967). The effect of thirst and a related verbal stimulus on dream
reports. Philosophical Dissertation, New York University.
Botman, H. I., & Crovitz, H. F. (1989a). Dream reports and autobiographical
memory. Imagination, Cognition and Personality, 9, 213–224.
Botman, H. I., & Crovitz, H. F. (1989b). Facilitating the reportage of dreams
with semantic cues. Imagination, Cognition and Personality, 9, 115–129.
Breger, L., Hunter, I., & Lane, R. W. (1971). The effect of stress on dreams.
New York: International Universities Press.
Brink, S. M., & Allan, J. A. B. (1992). Dreams of anorexic and bulimic women: a
research study. Journal of Analytical Psychology, 37, 275–297.
Brink, S. M., Allan, J. A., & Boldt, W. (1995). Symbolic representation of psycho-
logical states in the dream of women with eating disorders. Canadian Journal
of Counseling, 29, 332–344.
Broidy, L., & Agnew, R. (1997). Gender and crime: A general strain theory per-
spective. Journal of Research in Crime and Delinquency, 34(3), 275–306.
Bruni, O., Lo Reto, F., Recine, A., Ottaviano, S., & Guidetti, V. (1999).
Development and validation of a dream content questionnaire for school age
children. Sleep and Hypnosis, 1, 41–46.
Bryant, R. A., Wyzenbeek, M., & Weinstein, J. (2011). Dream rebound of sup-
pressed emotional thoughts: The influence of cognitive load. Consciousness and
Cognition, 20(3), 515–522.
Bulkeley, K. (2009). Seeking patterns in dream content: A systematic approach to
word searches. Consciousness and Cognition, 18, 905–916.
Bulkeley, K. (2014). Digital dream analysis: A revised method. Consciousness and
Cognition, 29, 159–170.
Bulkeley, K., & Domhoff, G. W. (2010). Detecting meaning in dream reports: An
extension of a word search approach. Dreaming, 20, 77–95.
Bulkeley, K., & Kahan, T. L. (2008). The impact of September 11 on dreaming.
Consciousness and Cognition, 17, 1248–1256.
Campbell, K. B., & Muller-Gass, A. (2011). The extent of processing of near-
hearing threshold stimuli during natural sleep. Sleep, 34, 1243–1249.
Carr, M., & Nielsen, T. (2017). A novel differential susceptibility framework for
the study of nightmares: Evidence for trait sensory processing sensitivity.
Clinical Psychology Review, 58, 86–96.
Carrasco, E., Santamaria, J., Iranzo, A., Pintor, L., De Pablo, J., Solanas, A.,
Kumru, H., Martinez-Rodrigez, J. E., & Boget, T. (2006). Changes in dream-
REFERENCES
187
DeDonato, A., Belicki, K., & Cuddy, M. (1996). Rater’s abilities to identify indi-
viduals reporting sexual abuse from nightmare content. Dreaming, 6, 33–41.
DeGennaro, L., & Violani, C. (1990). White dreams: The relationship between
the failure in dream recall and degree of hemispheric lateralization. Association
for the Study of Dreams Newsletter, 7(5), 7.
Dement, W. C. (1960). The effect of dream deprivation. Science, 131, 1705–1707.
Dement, W. C., & Kleitman, N. (1957). Cyclic variations in EEG during sleep and
their relation to eye movements, body motility and dreaming.
Electroencephalography and Clinical Neurophysiology, 9, 673–690.
Dement, W. C., & Wolpert, E. A. (1958). The relation of eye movements, body
motility and external stimuli to dream content. Journal of Experimental
Psychology, 44, 543–553.
Desseilles, M., Dang-Vu, T. T., Sterpenich, V., & Schwartz, S. (2011). Cognitive
and emotional processes during dreaming: A neuroimaging view. Consciousness
and Cognition: An International Journal, 20(4), 998–1008.
Diekelmann, S., Wilhelm, I., & Born, J. (2009). The whats and whens of sleep-
dependent memory consolidation. Sleep Medicine Reviews, 13, 309–321.
Dippel, B. (1988). Manual zur Erfassung des manifesten Trauminhaltes ([Link],
204 Items). München: Unveröffentlichtes Manuskript.
Dippel, B., Lauer, C., Riemann, D., Majer-Trendel, K., Krieg, J.-C., & Berger, M.
(1987). Sleep and dreams in eating disorders. Psychotherapy and Psychosomatics,
48, 165–169.
Dodet, P., Chavez, M., Leu-Semenescu, S., Golmard, J.-L., & Arnulf, I. (2015).
Lucid dreaming in narcolepsy. Sleep, 38(3), 487–497.
Domhoff, B. (1969). Home dreams versus laboratory dreams – Home dreams are
better. In M. Kramer, R. M. Whitman, B. J. Baldridge, & P. H. Ornstein (Eds.),
Dream psychology and the new biology of dreaming (pp. 199–217). Springfield:
Charles C. Thomas.
Domhoff, G. W. (1996). Finding meaning in dreams: A quantitative approach.
New York: Plenum Press.
Domhoff, G. W. (2003). The scientific study of dreams: Neural networks, cognitive
development and content analysis. Washington, DC: American Psychological
Association.
Domhoff, G. W. (2017). The invasion of the concept snatchers: The origins, dis-
tortions, and future of the continuity hypothesis. Dreaming, 27(1), 14–39.
Domhoff, G. W. (2018). The emergence of dreaming: Mind-wandering, embodied
simulation, and the default network. New York: Oxford University Press.
Domhoff, B., & Kamiya, J. (1964). Problems in dream content study with objec-
tive indicators: I. A comparison of home and laboratory dream reports. Archives
of General Psychiatry, 11, 519–524.
Domhoff, G. W., Meyer-Gomes, K., & Schredl, M. (2005–2006). Dreams as the
expression of conceptions and concerns: A comparison of German and American
college students. Imagination, Cognition & Personality, 25, 269–282.
190 REFERENCES
Dresler, M., Koch, S. P., Wehrle, R., Spoormaker, V. I., Holsboer, F., Steiger, A.,
Sämann, P. G., Obrig, H., & Czisch, M. (2011). Dreamed movement elicits
activation in the sensorimotor cortex. Current Biology, 21, 1833–1837.
Dresler, M., Wehrle, R., Spoormaker, V. I., Koch, S. P., Holsboer, F., Steiger, A.,
Obrig, H., Samann, P. G., & Czisch, M. (2012). Neural correlates of dream
lucidity obtained from contrasting lucid versus non-lucid REM sleep: A com-
bined EEG/fMRI case study. Sleep, 35, 1017–1020.
Duffey, T. H., Wooten, H. R., Lamadue, C. A., & Comstock, D. C. (2004). The
effects of dream sharing on marital intimacy and satisfaction. Journal of Couple
and Relationship Therapy, 3, 53–68.
Dyck, S., Schredl, M., & Kühnel, A. (2017). Lucid dream induction using three
different cognitive methods. International Journal of Dream Research, 10(2),
151–156.
Eagly, A. H. (1987). Sex differences in social behavior: A social-role interpretation.
Hillsdale: Lawrence Erlbaum.
Eagly, A. H., & Steffen, V. J. (1986). Gender and aggressive behavior: A meta-
analytic review of the social psychology literature. Psychological Bulletin, 100,
309–330.
Eichenlaub, J.-B., Bertrand, O., Morlet, D., & Ruby, P. (2014a). Brain reactivity
differentiates subjects with high and low dream recall frequencies during both
sleep and wakefulness. Cerebral Cortex, 24(5), 1206–1215.
Eichenlaub, J.-B., Nicolas, A., Daltrozzo, J., Redoute, J., Costes, N., & Ruby, P.
(2014b). Resting brain activity varies with dream recall frequency between sub-
jects. Neuropsychopharmacology, 39(7), 1594–1602.
Eigel, H. S. (1965). Die Träume der Manisch-Depressiven. Medizinische
Dissertation, Universität München.
Ellman, S. J., Spielman, A. J., Luck, D., Steiner, S. S., & Halperin, R. (1978).
REM deprivation: A review. In A. M. Arkin, J. S. Antrobus, & S. J. Ellman
(Eds.), The mind in sleep: Psychology and psychophysiology (pp. 419–457).
Hillsdale: Lawrence Erlbaum.
Enke, H., Ohlmeier, D., & Nast, J. (1968). Eine formale Affekt- und
Beziehungsanalyse in Traumserien von Patienten mit psychosomatischen
Krankheitsbildern. Zeitschrift für Psychosomatische Medizin, 9, 15–33.
Erdelyi, M. H. (2017). The continuity hypothesis. Dreaming, 27(4), 334–344.
Erlacher, D., & Schredl, M. (2004). Dreams reflecting waking sport activities: A
comparison of sport and psychology students. International Journal of Sport
Psychology, 35, 301–308.
Erlacher, D., & Schredl, M. (2010). Practicing a motor task in a lucid dream
enhances subsequent performance: A pilot study. Sport Psychologist, 24,
157–167.
Erlacher, D., Schredl, M., & LaBerge, S. (2003). Motor area activation during
dreamed hand clenching: A pilot study on EEG alpha band. Sleep and Hypnosis,
5, 182–187.
REFERENCES
191
Erlacher, D., Schredl, M., Watanabe, T., Yamana, J., & Gantzert, F. (2008). The
incidence of lucid dreaming within a Japanese university student sample.
International Journal of Dream Research, 1, 39–43.
Erlacher, D., Schädlich, M., Stumbrys, T., & Schredl, M. (2014). Time for actions
in lucid dreams: Effects of task modality, length, and complexity. Frontiers in
Psychology, 4. [Link]
Ermann, M. (1995). Die Traumerinnerung bei Patienten mit psychogenen
Schlafstörungen: Empirische Befunde und einige Folgerungen für das
Verständnis des Träumens. In W. Leuschner & S. Hau (Eds.), Traum und
Gedächtnis: Neue Ergebnisse aus psychologischer, psychoanalytischer und neuro-
physiologischer Forschung (pp. 165–186). Münster: LIT Verlag.
Etevenon, P., & Guillou, S. (1986). EEG cartography of a night of sleep and
dreams: A longitudinal study with provoked awakenings. Neuropsychobiology,
16, 146–151.
Fahrion, S. L. (1967). The relationship of heart rate and dream content in heart-
rate responders. Dissertation Abstracts, 27(9-B), 3307.
Fantini, M. L., & Ferini-Strambi, L. (2012). Dream content in RBD: Effect of
clonazepam. Sleep Medicine, 13, 1110–1111.
Fantini, M. L., Corona, A., Clerici, S., & Ferini-Strambi, L. (2005). Aggressive
dream content without daytime aggressiveness in REM sleep behavior disorder.
Neurology, 65, 1010–1015.
Faraday, A. (1990). The dream game. New York: Harper & Row.
Fell, J., Fernandez, G., Lutz, M. T., Kockelmann, E., Burr, W., Schaller, C., Elger,
C. E., & Helmstaedter, C. (2006). Rhinal-hippocampal connectivity deter-
mines memory formation during sleep. Brain, 129, 108–114.
Fiedler, K., & Hütter, M. (2014). Memory and emotion. In T. J. Perfect & D. S.
Lindsay (Eds.), The SAGE handbook of applied memory (pp. 145–161). London:
Sage.
Firth, H., & Oswald, I. (1975). Eye movements and visually active dreams.
Psychophysiology, 12, 602–606.
Fisher, C. (1966). Dreaming and sexuality. In R. M. Loewenstein, L. M. Newman,
M. Schur, & A. J. Solnit (Eds.), Psychoanalysis – A general psychology
(pp. 537–569). New York: International Universities Press.
Fisher, C., Gross, J., & Zuch, J. (1965). Cycle of penile erection synchronous with
dreaming (REM) sleep. Archives of General Psychiatry, 12, 29–45.
Fisher, C., Byrne, J., Edwards, A., & Kahn, E. (1970). A psychophysiological
study of nightmares. Journal of the American Psychoanalytic Association, 18,
747–782.
Fisher, S., Lewis, K. E., Bartle, I., Ghosal, R., Davies, L., & Blagrove, M. (2011).
Emotional content of dreams in obstructive sleep apnea hypopnea syndrome
patients and sleepy snorers attending a sleep-disordered breathing clinic.
Journal of Clinical Sleep Medicine, 7, 69–74.
192 REFERENCES
Flanagan, O. (2000). Dreaming souls: Sleep, dreams, and the evolution of the con-
scious mind. Oxford: Oxford University Press.
Fosse, M. J., Fosse, R., Hobson, J. A., & Stickgold, R. J. (2003). Dreaming and
episodic memory: A functional dissociation? Journal of Cognitive Neuroscience,
15, 1–9.
Foulkes, D. (1962). Dream reports from different stages of sleep. Journal of
Abnormal and Social Psychology, 65, 14–25.
Foulkes, D. (1978). A grammar of dreams. New York: Harvester Press.
Foulkes, D. (1982). Children’s dreams: Longitudinal studies. New York: Wiley.
Foulkes, D., & Fleisher, S. (1975). Mental activity in relaxed wakefulness. Journal
of Abnormal Psychology, 84, 66–75.
Foulkes, D., & Griffin, M. L. (1976). An experimental study of “creative dream-
ing”. Sleep Research, 5, 129.
Foulkes, D., & Rechtschaffen, A. (1964). Presleep determinants of dream con-
tent. Perceptual and Motor Skills, 19, 983–1005.
Foulkes, D., & Sheperd, J. (1971). Manual for a scoring system for children’s
dreams. Unpublished manuscript, University of Wyoming.
Foulkes, D., Pivik, T., Steadman, H. S., Spear, P. S., & Symonds, J. D. (1967).
Dreams of the male child: An EEG study. Journal of Abnormal Psychology, 72,
457–467.
Foulkes, D., Sullivan, B., Kerr, N. H., & Brown, L. (1988). Appropriateness of
dream feelings to dreamed situations. Cognition and Emotion, 2, 29–39.
Fox, K. C. R., Nijeboer, S., Solomonova, E., Domhoff, G. W., & Christoff, K.
(2013). Dreaming as mind wandering: Evidence from functional neuroimaging
and first-person content reports. Frontiers in Human Neuroscience, 7. https://
[Link]/10.3389/fnhum.2013.00412.
Frayn, D. H. (1991). The incidence and significance of perceptual qualities in the
reported dreams of patients with anorexia nervosa. Canadian Journal of
Psychiatry, 36, 517–520.
Freedman, N. (2017). Positive airway pressure treatment for obstructive sleep
apnea. In M. Kryger, T. Roth, & W. C. Dement (Eds.), Principles and practice
of sleep medicine (6th ed., pp. 1125–1137). Philadelphia: Elsevier.
Freud, S. (1900/1991). The interpretation of dreams (Org.: Die Traumdeutung).
London: Penguin Books.
Gackenbach, J., & LaBerge, S. (1986). An overview of lucid dreaming. In
A. Sheikh (Ed.), International review of mental imagery (Vol. 2, pp. 57–89).
New York: Human Sciences Press.
Gackenbach, J., Rosie, M., Bown, J., & Sample, T. (2011). Dream incorporation
of video-game play as a function of interactivity and fidelity. Dreaming, 21(1),
32–50.
Gaillard, J.-M., & Phelippeau, M. (1977). Analysis of dream contents by scaled
and rated measurements. Psychological Medicine, 7, 275–282.
REFERENCES
193
Gardner, R., Grossman, W. I., Roffwarg, H. P., & Weiner, H. (1975). The rela-
tionship of small limb movements during REM sleep to dreamed limb action.
Psychosomatic Medicine, 37, 147–159.
Gedda, L., & Brenci, G. (1979). Sleep and dream characteristics in twins. Acta
Geneticae Medicae et Gemellologiae, 28, 237–239.
Georgi, M., Schredl, M., Henley-Einion, J., & Blagrove, M. (2012). Gender dif-
ferences in dreaming in childhood and adolescence: The UK library study.
International Journal of Dream Research, 5, 125–129.
Germain, A., Krakow, B., Faucher, B., Zadra, A. L., Nielsen, T. A., Hollifield, M.,
Warner, T. D., & Koss, M. (2004). Increased mastery elements associated with
imagery rehearsal treatment for nightmares in sexual assault survivors with
PTSD. Dreaming, 14, 195–206.
Germain, A., Hall, M., Shear, M. K., Nofzinger, E. A., & Buysse, D. J. (2006).
Sleep disruption in PTSD: A pilot study with home-based polysomnography.
Sleep and Biological Rhythms, 4, 286–289.
Giambra, L. M., Jung, R. E., & Grodsky, A. (1996). Age changes in dream recall
in adulthood. Dreaming, 6, 17–31.
Gieselmann, A., Böckermann, M., Sorbi, M., & Pietrowsky, R. (2017). The effects
of an internet-based imagery rehearsal intervention: A randomized controlled
trial. Psychotherapy and Psychosomatics, 86(4), 231–240.
Giordano, P. L., & Spoto, G. (1977). Patient’s reports of their own sleep and
dream experience in psychopharmacological sleep research and treatment.
Activitas Nervose Superior, 19(Supplement 2), 370.
Glaubman, H., & Lewin, I. (1977). REM and dreaming. Perceptual and Motor
Skills, 44, 929–930.
Glucksman, M. L., & Kramer, M. (2017). Manifest dream content as a predictor
of suicidality. Psychodynamic Psychiatry, 45(2), 175–185.
Godin, I., Montplaisir, J., Gagnon, J.-F., & Nielsen, T. (2013). Alexithymia asso-
ciated with nightmare distress in idiopathic REM sleep behavior disorder. Sleep:
Journal of Sleep and Sleep Disorders Research, 36(12), 1957–1962.
Godin, I., Montplaisir, J., & Nielsen, T. (2015). Dreaming and nightmares in
REM sleep behavior disorder. Dreaming, 25(4), 257–273.
Goodenough, D. R., Shapiro, A., Holden, M., & Steinschriber, L. (1959). A com-
parison of “dreamers” and “nondreamers”. Journal of Abnormal and Social
Psychology, 59, 295–302.
Goodenough, D. R., Witkin, H. A., Koulack, D., & Cohen, H. (1975). The
effects of stress films on dream affect and on respiration and eye movement
activity during rapid-eye-movement sleep. Psychophysiology, 12, 313–320.
Gottschalk, L. A., Gleser, G., & Springer, K. J. (1963). Three hostility scales appli-
cable to verbal samples. Archives of General Psychiatry, 9, 254–279.
Gottschalk, L. A., Buchsbaum, M. J., Gillin, J. C., Wu, J. C., Reynolds, C. A., &
Herrera, D. B. (1991). Anxiety levels in dreams: Relation to localized cerebral
glucose metabolic rate. Brain Research, 538, 107–110.
194 REFERENCES
Herman, J. H., Erman, M., Boys, R., Preiser, L., Taylor, M. E., & Roffwarg, H. P.
(1984). Evidence for a directional correspondence between eye movements
and dream imagery in REM sleep. Sleep, 7, 52–63.
Hess, G., Schredl, M., & Goritz, A. S. (2016). Lucid dreaming frequency and the
Big Five personality factors. Imagination, Cognition and Personality, 36(3),
240–253.
Hill, C. E., & Knox, S. (2010). The use of dreams in modern psychotherapy.
International Review of Neurobiology, 92, 291–317.
Hill, C. E., Diemer, R. A., & Heaton, K. J. (1997). Dream interpretation sessions:
Who volunteers, who benefits, and what volunteer clients view as most and
least helpful. Journal of Counseling Psychology, 44, 53–62.
Hobson, J. A. (1988). The dreaming brain. New York: Basic Books.
Hobson, J. A. (1997). Dreaming as delirium: A mental status examination of our
nightly madness. Seminars in Neurology, 17, 121–128.
Hobson, J. A. (2009). REM sleep and dreaming: Towards a theory of protocon-
sciousness. Nature Reviews Neuroscience, 10(11), 803–813.
Hobson, J. A., & McCarley, R. W. (1977). The brain as a dream state generator:
An activation-synthesis hypothesis of the dream process. American Journal of
Psychiatry, 134, 1335–1348.
Hobson, J. A., & Schredl, M. (2011). The continuity and discontinuity between
waking and dreaming: A dialogue between Michael Schredl and Allan Hobson
concerning the adequacy and completeness of these notions. International
Journal of Dream Research, 4, 3–7.
Hobson, J. A., & Stickgold, R. (1994). Dreaming: A neurocognitive approach.
Consciousness and Cognition, 3, 1–15.
Hobson, J. A., & Stickgold, R. (1995). The conscious state paradigm: A neuro-
cognitive approach to waking, sleeping, and dreaming. In M. S. Gazzaniga
(Ed.), The cognitive neurosciences (pp. 1373–1388). Cambridge, MA: MIT
Press.
Hobson, J. A., & Voss, U. (2011). A mind to go out of: Reflections on primary
and secondary consciousness. Consciousness and Cognition, 20, 993–997.
Hobson, J. A., Hoffman, S. A., Helfand, R., & Kostner, D. (1987). Dream
bizarreness and the activation-synthesis hypothesis. Human Neurobiology, 6,
157–164.
Hobson, J. A., Pace-Schott, E. F., & Stickgold, R. (2000). Dreaming and the
brain: Toward a cognitive neuroscience of conscious states. Behavioral and
Brain Sciences, 23, 793–842.
Hoelscher, T. J., Klinger, E., & Barta, S. G. (1981). Incorporation of concern- and
nonconcern-related verbal stimuli into dream content. Journal of Abnormal
Psychology, 90, 88–91.
Hong, C. C., Gillin, J. C., Dow, B. M., Wu, J., & Buchsbaum, M. S. (1995).
Localized and lateralized cerebral glucose metabolism associated with eye
REFERENCES
197
Kahan, T. L., LaBerge, S., Levitan, L., & Zimbardo, P. (1997). Similarities and
differences between waking and dreaming cognition: An exploratory study.
Consciousness and Cognition, 6, 132–147.
Kahn, E., Dement, W., Fisher, C., & Barmack, J. E. (1962). Incidence of color in
immediately recalled dreams. Science, 137, 1054–1055.
Kalat, J. W. (2014). Biological psychology. Independence: Wadsworth.
Kallmeyer, R. J., & Chang, E. C. (1997). The multidimensional dream inventory:
Preliminary evidence for validity and reliability. Perceptual and Motor Skills, 85,
803–808.
Kellogg, E. W. (2017). The outer limits of lucid dreaming. International Journal
of Dream Research, 10(Suppl 1), S47–S48.
Kemp, S., Burt, C. D. B., & Sheen, M. (2003). Remembering dreamt and actual
experiences. Applied Cognitive Psychology, 17, 577–591.
Kern, S., Auer, A., Gutsche, M., Otto, A., Preuß, K., & Schredl, M. (2014).
Relation between waking politic, music and sports related tasks and dream con-
tent in students of politics and psychology students. International Journal of
Dream Research, 7, 80–84.
Kern, S., Appel, K., Schredl, M., & Pipa, G. (2017). No effect of α-GPC on lucid
dream induction or dream content. Somnologie, 21(3), 180–186.
Kerr, N. H., & Domhoff, G. W. (2004). Do the blind literally “see” in their
dreams? A critique of a recent claim that they do. Dreaming, 14, 230–233.
Kerr, N. H., Foulkes, D., & Schmidt, M. (1982). The structure of laboratory
dream reports in blind and sighted subjects. Journal of Nervous and Mental
Disease, 170, 286–294.
Klingenberg, B. (2008). Regression models for binary time series with gaps.
Computational Statistics and Data Analysis, 52(8), 4076–4090.
König, N., Mathes, J., & Schredl, M. (2016). Dreams and extraversion: A diary
study. International Journal of Dream Research, 9(2), 130–133.
König, N., Heizmann, L. M., Göritz, A. S., & Schredl, M. (2017). Colors in
dreams and the introduction of color TV in Germany: An online study.
International Journal of Dream Research, 10, 59–64.
Köthe, M., & Pietrowsky, R. (2001). Behavioral effects of nightmares and their
correlations to personality patterns. Dreaming, 11, 43–52.
Koukkou, M., & Lehmann, D. (1983). Dreaming: The functional state-shift
hypothesis. British Journal of Psychiatry, 142, 221–231.
Koulack, D. (1969). Effects of somatosensory stimulation on dream content.
Archives of General Psychiatry, 20, 718–725.
Koulack, D., & Goodenough, D. R. (1976). Dream recall and dream recall failure:
An arousal-retrieval model. Psychological Bulletin, 83, 975–984.
Kraehenmann, R., Pokorny, D., Vollenweider, L., Preller, K. H., Pokorny, T.,
Seifritz, E., & Vollenweider, F. X. (2017). Dreamlike effects of LSD on
waking imagery in humans depend on serotonin 2A receptor activation.
Psychopharmacology, 234(13), 2031–2046.
REFERENCES
199
Kramer, M., Schoen, L. S., & Kinney, L. (1984). The dream experience in dream-
disturbed Vietnam veterans. In B. A. Van der Kolk (Ed.), Posttraumatic stress
disorder: Psychological and biological sequelace (pp. 82–95). Washington, DC:
American Psychiatric Press.
Kröner-Borowik, T., Gosch, S., Hansen, K., Borowik, B., Schredl, M., & Steil, R.
(2013). The effects of suppressing intrusive thoughts on dream content, dream
distress and psychological parameters. Journal of Sleep Research, 22(5),
600–604.
Kroth, J., Gilbert, H., Guichard, A., & Quatman, T. (1999). Analysis of factor
structure in a dream inventory. Perceptual and Motor Skills, 89, 657–658.
Kunze, A. E., Arntz, A., Morina, N., Kindt, M., & Lancee, J. (2017). Efficacy of
imagery rescripting and imaginal exposure for nightmares: A randomized wait-
list controlled trial. Behaviour Research and Therapy, 97(Supplement C), 14–25.
Labelle, M.-A., Dang-Vu, T. T., Petit, D., Desautels, A., Montplaisir, J., & Zadra,
A. (2015). Sleep deprivation impairs inhibitory control during wakefulness in
adult sleepwalkers. Journal of Sleep Research, 24(6), 658–665.
LaBerge, S. P. (1980). Lucid dreaming: An exploratory study of consciousness dur-
ing sleep. Doctoral dissertation, Stanford University.
LaBerge, S. P. (1985). Lucid dreaming. Los Angeles: Jeremy P. Tarcher.
LaBerge, S. P., & Levitan, L. (1995). Validity established of dreamlight cues for
eliciting lucid dreaming. Dreaming, 5, 159–168.
LaBerge, S. P., Nagel, L. E., Dement, W. C., & Zarcone, V. P. (1981). Lucid
dreaming verified by volitional communication during REM sleep. Perceptual
and Motor Skills, 52, 727–732.
Lambrecht, S., Schredl, M., Henley-Einion, J., & Blagrove, M. (2013). Self-rated
effects of reading, TV viewing and daily activities on dreaming in adolescents
and adults: The UK library study. International Journal of Dream Research, 6,
41–44.
Lancee, J., & Schrijnemaekers, N. C. M. L. (2013). The association between
nightmares and daily distress. Sleep and Biological Rhythms, 11(1), 14–19.
Lancee, J., Spoormaker, V. I., & van den Bout, J. (2010). Cognitive-behavioral
self-help treatment for nightmares: A randomized controlled trial. Psychotherapy
and Psychosomatics, 79, 371–377.
Lauer, C., Riemann, D., Lund, R., & Berger, M. (1987). Shortened REM latency:
A consequence of psychological strain? Psychophysiology, 24, 263–271.
Leclair-Visonneau, L., Oudiette, D., Gaymard, B., Leu-Semenescu, S., & Arnulf,
I. (2010). Do the eyes scan dream images during rapid eye movement sleep?
Evidence from the rapid eye movement sleep behaviour disorder model. Brain,
133, 1737–1746.
Leslie, K., & Ogilvie, R. (1996). Vestibular dreams: The effect of rocking on
dream mentation. Dreaming, 6, 1–16.
REFERENCES
201
Leuschner, W., Hau, S., Brech, E., & Volk, S. (1994). Disassociation and reasso-
ciation of subliminally induced stimulus material in drawings of dreams and
drawings of waking free imagery. Dreaming, 4, 1–27.
Levin, R., & Fireman, G. (2002). Nightmare prevalence, nightmare distress, and
self-reported psychological disturbance. Sleep, 25, 205–212.
Levin, R., & Nielsen, T. A. (2007). Disturbed dreaming, posttraumatic stress dis-
order, and affect distress: A review and neurocognitive model. Psychological
Bulletin, 133, 482–528.
Levin, R., Fireman, G., Spendlove, S., & Pope, A. (2011). The relative contribu-
tion of affect load and affect distress as predictors of disturbed dreaming.
Behavioral Sleep Medicine, 9(3), 173–183.
Li, S. X., Zhang, B., Li, A. M., & Wing, Y. K. (2010). Prevalence and correlates of
frequent nightmares: A community-based 2-phase study. Sleep, 33, 774–780.
Li, S. X., Lam, S. P., Zhang, J., Yu, M. W. M., Chan, J. W. Y., Chan, C. S. Y.,
Espie, C. A., Freeman, D., Mason, O., & Wing, Y.-K. (2016). Sleep distur-
bances and suicide risk in an 8-year longitudinal study of schizophrenia-
spectrum disorders. Sleep, 39(6), 1275–1282.
Limosani, I., D’Agostino, A., Manzone, M. L., & Scarone, S. (2011). Bizarreness
in dream reports and waking fantasies of psychotic schizophrenic and manic
patients: Empirical evidences and theoretical consequences. Psychiatry Research,
189(2), 195–199.
Lloyd, S., & Cartwright, R. D. (1995). The collection of home and laboratory
dreams by means of an instrumental response technique. Dreaming, 5, 63–73.
Lortie-Lussier, M., Simond, S., Rinfret, N., & De Koninck, J. (1992). Beyond sex
differences: Family and occupational roles’ impact on women’s and men’s
dreams. Sex Roles, 26, 79–96.
Lusignan, F.-A., Zadra, A. L., Dubuc, M.-J., Daoust, A.-M., Mottard, J.-P., &
Godbout, R. (2009). Dream content in chronically-treated persons with
schizophrenia. Schizophrenia Research, 112, 164–173.
MacFarlane, J. G., & Wilson, T. L. (2006). A relationship between nightmare
content and somatic stimuli in a sleep-disordered population: A preliminary
study. Dreaming, 16, 53–59.
Malinowski, J. E., & Horton, C. L. (2014a). Evidence for the preferential incor-
poration of emotional waking-life experiences into dreams. Dreaming, 24(1),
18–31.
Malinowski, J. E., & Horton, C. L. (2014b). Memory sources of dreams: The
incorporation of autobiographical rather than episodic experiences. Journal of
Sleep Research, 23, 441–447.
Mangiaruga, A., Scarpelli, S., Bartolacci, C., & De Gennaro, L. (2018). Spotlight
on dream recall: The ages of dreams. Nature and Science of Sleep, 10, 1–12.
Maquet, P., Peters, J.-M., Aerts, J., Delfiore, G., Deguelde, C., Luxen, A., &
Franck, G. (1996). Functional neuroanatomy of human rapid-eye-movement
sleep and dreaming. Nature, 383, 163–166.
202 REFERENCES
Nielsen, T. A., & Powell, R. A. (1992). The day-residue and dream lag effects: A
literature review and limited replication of two temporal effects in dream for-
mation. Dreaming, 2, 67–77.
Nielsen, T. A., & Powell, R. A. (2015). Dreams of the rarebit fiend: Food and diet
as instigators of bizarre and disturbing dreams. Frontiers in Psychology, 6.
[Link]
Nielsen, T. A., McGregor, D. L., Zadra, A. L., Ilnicki, D., & Ouellet, L. (1993).
Pain in dreams. Sleep, 16, 490–498.
Nielsen, T. A., Oullet, L., Warnes, H., Cartier, A., Malo, J.-L., & Montplaisir,
J. (1997). Alexithymia and impoverished dream recall in asthmatic patients:
Evidence for self-report measures. Journal of Psychosomatic Research, 42, 53–59.
Nielsen, T. A., Kuiken, D., Alain, G., Stenstrom, P., & Powell, R. A. (2004).
Immediate and delayed incorporations of events into dreams: Further replica-
tion and implication for dream function. Journal of Sleep Research, 13, 327–336.
Nixon, O. L., Pierce, C. M., Lester, B. K., & Matthis, J. L. (1964). Narcolepsy:
Nocturnal dream frequency in adolescents. Journal of Neuropsychiatry, 5,
150–152.
Noble, D. (1950). A study of dreams in schizophrenia and allied states. American
Journal of Psychiatry, 107, 612–616.
Noreika, V., Valli, K., Markkula, J., Seppälä, K., & Revonsuo, A. (2010). Dream
bizarreness and waking thought in schizophrenia. Psychiatry Research, 178(3),
562–564.
Ohayon, M. M., Morselli, P. L., & Guilleminault, C. (1997). Prevalence of night-
mares and their relationship to psychopathology and daytime functioning in
insomnia subjects. Sleep, 20, 340–348.
Okorome Mume, C. (2009). Nightmare in schizophrenic and depressed patients.
European Journal of Psychiatry, 23, 177–183.
Okuma, T., Fukuma, E., & Kobayashi, K. (1975). “Dream detector” and com-
parison of laboratory and home dreams collected by REMP-awakening tech-
nique. In E. D. Weitzman (Ed.), Advances in sleep research (Vol. 2, pp. 223–231).
New York: Spectrum Publications.
Oliver, M. B., & Hyde, J. S. (1993). Gender differences in sexuality: A meta-
analysis. Psychological Bulletin, 114, 29–51.
Olsen, M. R., Schredl, M., & Carlsson, I. (2013). Sharing dreams: Frequency,
motivations, and relationship intimacy. Dreaming, 23(4), 245–255.
Ornstein, P. H., Whitman, R. M., Kramer, M., & Baldridge, B. J. (1969). Drugs
and dreams IV: Tranquilizer and their effects upon dreams and dreaming in
schizophrenic patients. Experimental Medicine and Surgery, 27, 145–156.
Oudiette, D., Leu, S., Pottier, M., Buzare, M.-A., Brion, A., & Arnulf, I. (2009).
Dreamlike mentations during sleepwalking and sleep terrors in adults. Sleep, 32,
1621–1627.
Pace-Schott, E. F., Gersh, T., Silvestri, R., Stickgold, R., Salzman, C., & Hobson,
J. A. (2001). SSRI treatment suppresses dream recall frequency but increases
REFERENCES
205
Robert, G., & Zadra, A. L. (2014). Thematic and content analysis of idiopathic
nightmares and bad dreams. Sleep: Journal of Sleep and Sleep Disorders Research,
37(2), 409–417.
Roffwarg, H. P., Dement, W. C., Muzio, J. N., & Fisher, C. (1962). Dream imag-
ery: Relationship to rapid eye movements of sleep. Archives of General
Psychiatry, 7, 235–258.
Roffwarg, H. P., Herman, J. H., Bowe-Anders, C., & Tauber, E. S. (1978). The
effects of sustained alterations of waking visual input on dream content. In
A. M. Arkin, J. S. Antrobus, & S. J. Ellman (Eds.), The mind in sleep: Psychology
and psychophysiology (pp. 295–349). Hillsdale: Lawrence Erlbaum.
Rosenlicht, N., Maloney, T., & Feinberg, I. (1994). Dream report length is more
dependent on arousal level than prior REM duration. Brain Research Bulletin,
34, 99–101.
Ross, R. J., Ball, W. A., Sullivan, K. A., & Caroff, S. N. (1989). Sleep disturbances
as the hallmark of posttraumatic stress disorder. American Journal of Psychiatry,
146, 697–707.
Rost, J. (1996). Lehrbuch Testtheorie. Bern: Huber.
Roth, B., & Bruhova, S. (1969). Dreams in narcolepsy, hypersomnia and dissoci-
ated sleep disorders. Experimental Medicine and Surgery, 27, 187–209.
Roussy, F., Raymond, I., Gonthier, I., Grenier, J., & De Koninck, J. (1998).
Temporal references in manifest dream content: Confirmation of increased
remoteness as the night progresses. Sleep Supplement, 21, 285.
Röver, S. A., & Schredl, M. (2017). Measuring emotions in dreams: Effects of
dream length and personality. International Journal of Dream Research, 10(1),
65–68.
Saint-Denys, H. de (1982). Dreams and how to guide them (Original: 1867).
London: Duckworth.
Samson, H., & De Koninck, J. (1986). Continuity or compensation between wak-
ing and dreaming: An exploration using the Eysenck Personality Inventory.
Psychological Reports, 58, 871–874.
Sandman, N., Valli, K., Kronholm, E., Ollila, H. M., Revonsuo, A., Laatikainen,
T., & Paunio, T. (2013). Nightmares: Prevalence among the Finnish general
adult population and war veterans during 1972–2007. Sleep, 36, 1041–1050.
Sándor, P., Szakadát, S., Kertész, K., & Bódizs, R. (2015). Content analysis of 4
to 8 year-old children’s dream reports. Frontiers in Psychology, 6. [Link]
org/10.3389/fpsyg.2015.00534.
Saul, L., Sheppard, E., Selby, D., Lhamon, W., & Sachs, D. (1954). The quantifi-
cation of hostility in dreams with reference to essential hypertension. Science,
119, 382–383.
Saunders, D. T., Roe, C. A., Smith, G., & Clegg, H. (2016). Lucid dreaming
incidence: A quality effects meta-analysis of 50 years of research. Consciousness
and Cognition, 43, 197–215.
208 REFERENCES
Saunders, D. T., Clegg, H., Roe, C. A., & Smith, G. D. (2017). Exploring the role
of need for cognition, field independence and locus of control on the incidence
of lucid dreams during a 12-week induction study. Dreaming, 27(1), 68–86.
Scarone, S., Manzone, M. L., Gambini, O., Kantzas, I., Limosani, I., D’Agostino,
A., & Hobson, J. A. (2008). The dream as a model for psychosis: An experi-
mental approach using bizarreness as a cognitive marker. Schizophrenia Bulletin,
34, 515–522.
Schädlich, M., & Erlacher, D. (2012). Applications of lucid dreams: An online
study. International Journal of Dream Research, 5, 134–138.
Schädlich, M., Erlacher, D., & Schredl, M. (2017). Improvement of darts perfor-
mance following lucid dream practice depends on the number of distractions
while rehearsing within the dream – A sleep laboratory pilot study. Journal of
Sports Sciences, 35(23), 2365–2372.
Schäfer, V., & Bader, K. (2009). The impact of early-life maltreatment on dreams
of patients with insomnia. International Journal of Dream Research, 2, 18–26.
Schenck, C. H., Scott, R., Ettinger, M. G., & Mahowald, M. W. (1986). Chronic
behavioral disorders of human REM sleep: A new category of parasomnia.
Sleep, 9, 293–308.
Schmidt, R. E., & Gendolla, G. H. E. (2008). Dreaming of white bears: The
return of the suppressed at sleep onset. Consciousness and Cognition, 17(3),
714–724.
Schonbar, R. A. (1965). Differential dream recall frequency as a component of
“life-style”. Journal of Consulting Psychology, 29, 468–474.
Schredl, M. (1991). Traumerinnerungshäufigkeit und Trauminhalt bei
Schlafgestörten, psychiatrischen Patienten und Gesunden. Unveröffentlichte
Diplomarbeit, Universität Mannheim.
Schredl, M. (1998a). Dream content in patients with narcolepsy: Preliminary find-
ings. Dreaming, 8, 103–107.
Schredl, M. (1998b). The stability and variability of dream content. Perceptual
and Motor Skills, 86, 733–734.
Schredl, M. (1998c). Träume und Schlafstörungen: Empirische Studie zur
Traumerinnerungshäufigkeit und zum Trauminhalt schlafgestörter PatientInnen.
Marburg: Tectum.
Schredl, M. (1999a). Die nächtliche Traumwelt: Eine Einführung in die psycholo-
gische Traumforschung. Stuttgart: Kohlhammer.
Schredl, M. (1999b). The problem of dream length in analysis of content.
Perceptual and Motor Skills, 88, 434–436.
Schredl, M. (2000a). Continuity between waking life and dreaming: Are all wak-
ing activities reflected equally often in dreams. Perceptual and Motor Skills, 90,
844–846.
Schredl, M. (2000b). The effect of dreams on waking life. Sleep and Hypnosis, 2,
120–124.
REFERENCES
209
Schredl, M. (2000c). Time series analysis in dream research. Perceptual and Motor
Skills, 91, 915–916.
Schredl, M. (2001a). Dream recall frequency and sleep quality of patients with
restless legs syndrome. European Journal of Neurology, 8, 185–189.
Schredl, M. (2001b). Dreams of singles: Effects of waking-life social contacts on
dream content. Personality and Individual Differences, 31, 269–275.
Schredl, M. (2002). Questionnaire and diaries as research instruments in dream
research: Methodological issues. Dreaming, 12, 17–26.
Schredl, M. (2003a). Continuity between waking and dreaming: A proposal for a
mathematical model. Sleep and Hypnosis, 5, 38–52.
Schredl, M. (2003b). Effects of state and trait factors on nightmare frequency.
European Archives of Psychiatry and Clinical Neuroscience, 253, 241–247.
Schredl, M. (2004a). Reliability and stability of a dream recall frequency scale.
Perceptual and Motor Skills, 98, 1422–1426.
Schredl, M. (2004b). Traumerinnerung: Modelle und empirische Untersuchungen.
Marburg: Tectum.
Schredl, M. (2006). Factors affecting the continuity between waking and dream-
ing: Emotional intensity and emotional tone of the waking-life event. Sleep and
Hypnosis, 8, 1–5.
Schredl, M. (2007). Dream recall: Models and empirical data. In D. Barrett &
P. McNamara (Eds.), The new science of dreaming – Volume 2: Content, recall,
and personality correlates (pp. 79–114). Westport: Praeger.
Schredl, M. (2008a). Determining the dreamer’s gender from a single dream
report: A matching study. International Journal of Dream Research, 1, 23–26.
Schredl, M. (2008b). Dream recall frequency in a representative German sample.
Perceptual and Motor Skills, 106, 699–702.
Schredl, M. (2008c). Laboratory references in dreams: Methodological problem
and/or evidence for the continuity hypothesis of dreaming? International
Journal of Dream Research, 1, 3–6.
Schredl, M. (2008d). Personality correlates of flying dreams. Imagination,
Cognition and Personality, 27, 129–137.
Schredl, M. (2008e). Spontaneously reported colors in dreams: Correlations with
attitude towards creativity, personality and memory. Sleep and Hypnosis, 10,
54–60.
Schredl, M. (2008f). Traum. München: Reinhardt/UTB.
Schredl, M. (2009a). Effect of dreams on daytime mood: The effects of gender
and personality. Sleep and Hypnosis, 11, 51–57.
Schredl, M. (2009b). Home dream recall in children and young adults.
International Journal of Dream Research, 2, 58–59.
Schredl, M. (2009c). Nightmare frequency in patients with primary insomnia.
International Journal of Dream Research, 2, 85–88.
210 REFERENCES
Schredl, M., & Doll, E. (1997). Autogenic training and dream recall. Perceptual
and Motor Skills, 84, 1305–1306.
Schredl, M., & Doll, E. (1998). Emotions in diary dreams. Consciousness and
Cognition, 7, 634–646.
Schredl, M., & Engelhardt, H. (2001). Dreaming and psychopathology: Dream
recall and dream content of psychiatric inpatients. Sleep and Hypnosis, 3, 44–54.
Schredl, M., & Erlacher, D. (2003). The problem of dream content analysis valid-
ity as shown by a bizarreness scale. Sleep and Hypnosis, 5, 129–135.
Schredl, M., & Erlacher, D. (2004). Lucid dreaming frequency and personality.
Personality and Individual Differences, 37, 1463–1473.
Schredl, M., & Erlacher, D. (2007). Self-reported effects of dreams on waking-life
creativity: An empirical study. Journal of Psychology, 141, 35–46.
Schredl, M., & Erlacher, D. (2008). Relationship between waking sport activities,
reading and dream content in sport and psychology students. Journal of
Psychology, 142, 267–275.
Schredl, M., & Erlacher, D. (2010). Is sleep-dependent memory consolidation of
a visuo-motor task related to dream content? International Journal of Dream
Research, 3, 74–79.
Schredl, M., & Erlacher, D. (2011). Frequency of lucid dreaming in a representa-
tive German sample. Perceptual and Motor Skills, 111, 60–64.
Schredl, M., & Fulda, S. (2005a). Dream recall and sleep duration: State or trait
factor. Perceptual and Motor Skills, 101, 613–616.
Schredl, M., & Fulda, S. (2005b). Reliability and stability of dream recall fre-
quency. Dreaming, 15, 240–244.
Schredl, M., & Göritz, A. S. (2014). Umgang mit Alpträumen in der
Allgemeinbevölkerung: Eine Online-Studie. [Coping with nightmares in the
general population: An online study]. Psychotherapie, Psychosomatik und
Medizinische Psychologie, 64(5), 192–196.
Schredl, M., & Göritz, A. S. (2015). Changes in dream recall frequency, night-
mare frequency, and lucid dream frequency over a 3-year period. Dreaming,
25(2), 81–87.
Schredl, M., & Göritz, A. S. (2017). Dream recall frequency, attitude toward
dreams, and the Big Five personality factors. Dreaming, 27(1), 49–58.
Schredl, M., & Göritz, A. S. (2018). Nightmare themes: An online study of most
recent nightmares and childhood nightmares. Journal of Clinical Sleep
Medicine, 14(3), 465–471.
Schredl, M., & Hofmann, F. (2003). Continuity between waking activities and
dream activities. Consciousness and Cognition, 12, 298–308.
Schredl, M., & Keller, K. (2008–2009). Dream content in a representative German
sample: Gender differences and the effects of other socio-demographic vari-
ables. Imagination, Cognition and Personality, 28, 37–48.
212 REFERENCES
Schredl, M., & Montasser, A. (1996). Dream recall: State or trait variable? Part II:
State factors, investigations, and final conclusions. Imagination, Cognition and
Personality, 16, 231–261.
Schredl, M., & Montasser, A. (1999). Dreaming and eating disorders. Sleep and
Hypnosis, 1, 225–231.
Schredl, M., & Noveski, A. (2017). Lucid dreaming: A diary study. Imagination,
Cognition and Personality. [Link]
Schredl, M., & Pallmer, R. (1998). Geschlechtsunterschiede in Angstträumen von
SchülerInnen. Praxis der Kinderpsychologie und Kinderpsychiatrie, 47, 463–476.
Schredl, M., & Piel, E. (2003). Gender differences in dream recall frequency: Data
from four representative German samples. Personality and Individual
Differences, 35, 1185–1189.
Schredl, M., & Piel, E. (2004). War-related dream themes in Germany from 1956
to 2000. Journal of Sleep Research Supplement, 13(1), 658.
Schredl, M., & Piel, E. (2005). Gender differences in dreaming: Are they stable
over time? Personality and Individual Differences, 39, 309–316.
Schredl, M., & Piel, E. (2006). War-related dream themes in Germany from 1956
to 2000. Political Psychology, 27, 299–307.
Schredl, M., & Reinhard, I. (2008a). Dream recall, dream length and sleep dura-
tion: State or trait factor. Perceptual and Motor Skills, 106, 633–636.
Schredl, M., & Reinhard, I. (2008b). Gender differences in dream recall: A meta-
analysis. Journal of Sleep Research, 17, 125–131.
Schredl, M., & Reinhard, I. (2009–2010). The continuity between waking mood
and dream emotions: Direct and second-order effects. Imagination, Cognition
and Personality, 29, 271–282.
Schredl, M., & Reinhard, I. (2011). Gender differences in nightmare frequency: A
meta-analysis. Sleep Medicine Reviews, 15, 115–121.
Schredl, M., & Reinhard, I. (2012). Frequency of a romantic partner in a dream
series. Dreaming, 22(4), 223–229.
Schredl, M., & Schawinski, J. A. (2010). Frequency of dream sharing: The effects
of gender and personality. American Journal of Psychology, 123, 93–101.
Schredl, M., & Schmitt, J. (2009). Dream recall frequency and nightmare fre-
quency in patients with sleep disordered breathing. Somnologie, 13, 12–17.
Schredl, M., Kleinferchner, P., & Gell, T. (1996a). Dreaming and personality:
Thick vs. thin boundaries. Dreaming, 6, 219–223.
Schredl, M., Schröder, A., & Löw, H. (1996b). Traumerleben von älteren
Menschen – Teil 2: Empirische Studie und Diskussion. Zeitschrift für
Gerontopsychologie und -psychiatrie, 9, 43–53.
Schredl, M., Jochum, S., & Souguenet, S. (1997). Dream recall, visual memory,
and absorption in imaginings. Personality and Individual Differences, 22,
291–292.
REFERENCES
213
Schredl, M., Sahin, V., & Schäfer, G. (1998a). Gender differences in dreams: Do
they reflect gender differences in waking life? Personality and Individual
Differences, 25, 433–442.
Schredl, M., Schäfer, G., Weber, B., & Heuser, I. (1998b). Dreaming and insom-
nia: Dream recall and dream content of patients with insomnia. Journal of Sleep
Research, 7, 191–198.
Schredl, M., Dombrowe, C., Bozzer, A., & Morlock, M. (1999a). Do subliminal
stimuli affect dream content? Methodological issues and empirical data. Sleep
and Hypnosis, 1, 181–185.
Schredl, M., Kraft-Schneider, B., Kröger, H., & Heuser, I. (1999b). Dream con-
tent of patients with sleep apnea. Somnologie, 3, 319–323.
Schredl, M., Schäfer, G., Hofmann, F., & Jacob, S. (1999c). Dream content and
personality: Thick vs. thin boundaries. Dreaming, 9, 257–263.
Schredl, M., Bohusch, C., Kahl, J., Mader, A., & Somesan, A. (2000). The use of
dreams in psychotherapy: A survey of psychotherapists in private practice.
Journal of Psychotherapy Practice and Research, 9, 81–87.
Schredl, M., Kronenberg, G., Nonell, P., & Heuser, I. (2001). Dream recall,
nightmare frequency, and nocturnal panic attacks in patients with panic disor-
der: Their relationship to nocturnal panic attacks. Journal of Nervous and
Mental Disease, 189, 559–562.
Schredl, M., Brenner, C., & Faul, C. (2002). Positive attitude toward dreams:
Reliability and stability of a ten-item scale. North American Journal of Psychology,
4, 343–346.
Schredl, M., Ciric, P., Bishop, A., Gölitz, E., & Buschtöns, D. (2003a). Content
analysis of German students’ dreams: Comparison to American findings.
Dreaming, 13, 237–243.
Schredl, M., Landgraf, C., & Zeiler, O. (2003b). Nightmare frequency, nightmare
distress and neuroticism. North American Journal of Psychology, 5, 345–350.
Schredl, M., Wittmann, L., Ciric, P., & Götz, S. (2003c). Factors of home dream
recall: A structural equation model. Journal of Sleep Research, 12, 133–141.
Schredl, M., Burchert, N., & Grabatin, Y. (2004a). The effect of training on inter-
rater reliability in dream content analysis. Sleep and Hypnosis, 6, 139–144.
Schredl, M., Schwenger, C., & Dehe, A. (2004b). Gender differences in dreams:
A matching study. Counseling and Clinical Psychology Journal, 1, 61–67.
Schredl, M., Schmitt, J., Hein, G., Schmoll, T., Eller, S., & Haaf, J. (2006).
Nightmares and oxygen desaturations: Is sleep apnea related to heightened
nightmare frequency? Sleep and Breathing, 10, 203–209.
Schredl, M., Fuchedzhieva, A., Hämig, H., & Schindele, V. (2008). Do we think
dreams are in black and white due to memory problems? Dreaming, 18,
175–180.
Schredl, M., Atanasova, D., Hörmann, K., Maurer, J. T., Hummel, T., & Stuck,
B. A. (2009a). Information processing during sleep: The effect of olfactory
214 REFERENCES
stimuli on dream content and dream emotions. Journal of Sleep Research, 18,
285–290.
Schredl, M., Bocklage, A., Engelhardt, J., & Mingebach, T. (2009b). Psychological
boundaries, dream recall, and nightmare frequency: A new Boundary
Personality Questionnaire (BPQ). International Journal of Dream Research, 2,
12–19.
Schredl, M., Desch, S., Röming, F., & Spachmann, A. (2009c). Erotic dreams and
their relationship to waking-life sexuality. Sexologies, 18, 38–43.
Schredl, M., Hebel, M. E., Klütsch, R. C., & Liehe, L. J. (2009d). The role of
mood congruency memory effects in dream recall: A pilot study. Dreaming, 19,
113–118.
Schredl, M., Riemann, D., & Berger, M. (2009e). The effect of trimipramine on
dream recall and dream emotions in depressive outpatients. Psychiatry Research,
167, 279–286.
Schredl, M., Becker, K., & Feldman, E. (2010a). Predicting the dreamer’s gender
from a single dream report: A matching study in a non-student sample.
International Journal of Dream Research, 3, 130–133.
Schredl, M., Lahl, O., & Göritz, A. S. (2010b). Gender, sex role orientation, and
dream recall frequency. Dreaming, 20, 19–24.
Schredl, M., Paul, F., Lahl, O., & Göritz, A. S. (2010–2011). Gender differences
in dream content: Related to biological sex or sex role orientation? Imagination,
Cognition, and Personality, 30, 171–183.
Schredl, M., Binder, R., Feldmann, S., Göder, R., Hoppe, J., Schmitt, J.,
Schweitzer, M., Specht, M., & Steinig, J. (2012a). Dreaming in patients with
sleep disorders: A multicenter study. Somnologie, 16, 32–42.
Schredl, M., Paul, F., Reinhard, I., Ebner-Priemer, U. W., Schmahl, C., & Bohus,
M. (2012b). Sleep and dreaming in patients with borderline personality disor-
der: A polysomnographic study. Psychiatry Research, 200, 430–436.
Schredl, M., Brennecke, J., & Reinhard, I. (2013a). Does training increase NREM
dream recall? A pilot study. International Journal of Dream Research, 6, 54–58.
Schredl, M., Kim, E., Labudek, S., Schädler, A., & Göritz, A. S. (2013b). Gender,
sex role orientation, and dreaming. Dreaming, 23(4), 277–286.
Schredl, M., Berres, S., Klingauf, A., Schellhaas, S., & Göritz, A. S. (2014a). The
Mannheim Dream questionnaire (MADRE): Retest reliability, age and gender
effects. International Journal of Dream Research, 7, 141–147.
Schredl, M., Hoffmann, L., Sommer, J. U., & Stuck, B. A. (2014b). Olfactory
stimulation during sleep can reactivate odor-associated images. Chemosensory
Perception, 7, 140–146.
Schredl, M., Buscher, A., Haaß, C., Scheuermann, M., & Uhrig, K. (2015a).
Gender differences in dream socialisation in children and adolescents.
International Journal of Adolescence and Youth, 20, 61–68.
REFERENCES
215
Schredl, M., Kim, E., Labudek, S., Schädler, A., & Göritz, A. S. (2015b). Factors
affecting the gender difference in dream sharing frequency. Imagination,
Cognition and Personality, 34(3), 306–316.
Schredl, M., Henley-Einion, J., & Blagrove, M. (2016a). Lucid dreaming and
personality in children/adolescents and adults: The UK library study.
International Journal of Dream Research, 9, 75–78.
Schredl, M., Stumbrys, T., & Erlacher, D. (2016b). Dream recall, nightmare fre-
quency, and spirituality. Dreaming, 26(1), 1–9.
Schredl, M., Kälberer, A., Zacharowski, K., & Zimmermann, M. (2017). Pain
dreams and dream emotions in patients with chronic back pain and healthy
controls. Open Pain Journal, 10, 65–72.
Schwitzgebel, E. (2002). Why did we think we dreamed in black and white?
Studies in History and Philosophy of Science, 33, 649–660.
Seda, G., Sanchez-Ortuno, M. M., Welsh, C. H., Halbower, A. C., & Edinger,
J. D. (2015). Comparative meta-analysis of prazosin and imagery rehearsal
therapy for nightmare frequency, sleep quality, and posttraumatic stress. Journal
of Clinical Sleep Medicine, 11(1), 11–22.
Selterman, D., Apetroaia, A., & Waters, E. (2012). Script-like attachment repre-
sentations in dreams containing current romantic partners. Attachment &
Human Development, 14(5), 501–515.
Shimizu, A., & Inoue, T. (1986). Dreamed speech and speech muscle activity.
Psychophysiology, 23, 210–214.
Siclari, F., Baird, B., Perogamvros, L., Bernardi, G., LaRocque, J. J., Riedner, B.,
Boly, M., Postle, B. R., & Tononi, G. (2017). The neural correlates of dream-
ing. Nature Neuroscience, 20, 872–878.
Siegel, J. M. (2017). Rapid eye movement sleep. In M. Kryger, T. Roth, & W. C.
Dement (Eds.), Principles and practice of sleep medicine (6th ed., pp. 78–95).
Philadelphia: Elsevier.
Sikka, P., Feilhauer, D., Valli, K., & Revonsuo, A. (2017). How you measure is
what you get: Differences in self- and external ratings of emotional experiences
in home dreams. American Journal of Psychology, 130(3), 367–384.
Sikka, P., Revonsuo, A., Sandman, N., Tuominen, J., & Valli, K. (2018). Dream
emotions: A comparison of home dream reports with laboratory early and late
REM dream reports. Journal of Sleep Research, 27, 206–214.
Silber, M. H., St. Louis, E. K., & Boeve, B. F. (2017). Rapid eye movement sleep
parasomnias. In M. Kryger, T. Roth, & W. C. Dement (Eds.), Principles and
practice of sleep medicine (6th ed., pp. 993–1001). Philadelphia: Elsevier.
Skancke, J., Holsen, I., & Schredl, M. (2014). Continuity between waking life and
dreams of psychiatric patients: A review and discussion of the implications for
dream research. International Journal of Dream Research, 7, 39–53.
Snyder, F. (1970). The phenomenology of dreaming. In L. Madow & L. H. Snow
(Eds.), The psychodynamic implications of the physiological studies on dreams
(pp. 124–151). Springfield: Charles C. Thomas.
216 REFERENCES
Strauch, I., & Meier, B. (1996). In search of dreams: Results of experimental dream
research. Albany: State University of New York Press.
Strelen, J. O. (2005). Akustisch evozierte Potentiale bei luziden Träumen – eine
Untersuchung über diskriminierendes Wahrnehmen und selektives Beantworten
von Tönen in REM-Schlaf, Dissertation, Mainz.
Stumbrys, T. (2011). Lucid dreaming: Discontinuity or continuity in conscious-
ness? International Journal of Dream Research, 4, 93–97.
Stumbrys, T., & Erlacher, D. (2014). The science of lucid dream induction. In
R. Hurd & K. Bulkeley (Eds.), Lucid dreaming: New perspectives on conscious-
ness in sleep, Science, psychology, and education (Vol. 1, pp. 77–102). Santa
Barbara: Praeger.
Stumbrys, T., & Erlacher, D. (2016a). Applications of lucid dreams and their
effects on the mood upon awakening. International Journal of Dream Research,
9(2), 146–150.
Stumbrys, T., & Erlacher, D. (2016b). Mindfulness and lucid dream frequency
predicts the ability to control lucid dreams. Imagination, Cognition and
Personality, 36(3), 229–239.
Stumbrys, T., Erlacher, D., Schädlich, M., & Schredl, M. (2012). Induction of
lucid dreams: A systematic review of evidence. Consciousness and Cognition,
21(3), 1456–1475.
Stumbrys, T., Erlacher, D., & Schredl, M. (2013a). Reliability and stability of
lucid dream and nightmare frequency scales. International Journal of Dream
Research, 6, 123–126.
Stumbrys, T., Erlacher, D., & Schredl, M. (2013b). Testing the involvement of
the prefrontal cortex in lucid dreaming: A tDCS study. Consciousness and
Cognition, 22(4), 1214–1222.
Stumbrys, T., Erlacher, D., Johnson, M., & Schredl, M. (2014). The phenome-
nology of lucid dreaming: An online survey. American Journal of Psychology,
127(2), 191–204.
Stumbrys, T., Erlacher, D., & Malinowski, P. (2015). Meta-awareness during day
and night: The relationship between mindfulness and lucid dreaming.
Imagination, Cognition and Personality, 34(4), 415–433.
Stumbrys, T., Erlacher, D., & Schredl, M. (2016). Effectiveness of motor practice
in lucid dreams: A comparison with physical and mental practice. Journal of
Sports Sciences, 34(1), 27–34.
Swart, M. L., van Schagen, A. M., Lancee, J., & van den Bout, J. (2013).
Prevalence of nightmare disorder in psychiatric outpatients. Psychotherapy and
Psychosomatics, 82(4), 267–268.
Takeuchi, T., Ogilvie, R. D., Ferrelli, A. V., Murphy, T. I., & Belicki, K. (2001).
The dream property scale: An exploratory English version. Consciousness and
Cognition, 10, 341–355.
218 REFERENCES
Valipour, A., Lothaller, H., Rauscher, H., Zwick, H., Burghuber, O. C., & Lavie,
P. (2007). Gender-related differences in symptoms of patients with suspected
breathing disorders in sleep: A clinical population study using the sleep disor-
ders questionnaire. Sleep, 30, 306–313.
Vallat, R., Meunier, D., Nicolas, A., & Ruby, P. (2017a). Sleep inertia and func-
tional connectivity between brain regions at awakening: An EEG-fMRI study.
International Journal of Dream Research, 10(Suppl 1), S59.
Vallat, R., Lajnef, T., Eichenlaub, J.-B., Berthomier, C., Jerbi, K., Morlet, D., &
Ruby, P. M. (2017b). Increased evoked potentials to arousing auditory stimuli
during sleep: Implication for the understanding of dream recall. Frontiers in
Human Neuroscience, 11, 132. [Link]
Vallat, R., Meunier, D., Nicolas, A., & Ruby, P. (2017c). Sleep inertia and func-
tional connectivity between brain regions at awakening: An EEG-fMRI study.
International Journal of Dream Research, 10(Suppl 1), S59.
Valli, K., Frauscher, B., Gschliesser, V., Wolf, E., Falkenstetter, T., Schönwald,
S. V., Ehrmann, L., Zangerl, A., Marti, I., Boesch, S. M., Revonsuo, A., Poewe,
W., & Högl, B. (2012). Can observers link dream content to behaviours in
rapid eye movement sleep behaviour disorder? A cross-sectional experimental
pilot study. Journal of Sleep Research, 21, 21–29. [Link]
j.1365-2869.2011.00938.x.
Van den Bulck, J., Çetin, Y., Terzi, Ö., & Bushman, B. J. (2016). Violence, sex,
and dreams: Violent and sexual media content infiltrate our dreams at night.
Dreaming, 26(4), 271–279.
Van Eeden, F. (1913). A study of dreams. Proceedings of the Society for Psychical
Research, 26, 431–461.
van Rijn, E., Eichenlaub, J. B., Lewis, P. A., Walker, M. P., Gaskell, M. G.,
Malinowski, J. E., & Blagrove, M. (2015). The dream-lag effect: Selective pro-
cessing of personally significant events during Rapid Eye Movement sleep, but
not during Slow Wave Sleep. Neurobiology of Learning and Memory, 122,
98–109.
van Schagen, A. M., Lancee, J., Spoormaker, V. I., & van den Bout, J. (2016).
Long-term treatment effects of imagery rehearsal therapy for nightmares in a
population with diverse psychiatric disorders. International Journal of Dream
Research, 9, 67–70.
van Schagen, A. M., Lancee, J., Swart, M., Spoormaker, V., & van den Bout,
J. (2017). Nightmare disorder, psychopathology levels, and coping in a diverse
psychiatric sample. Journal of Clinical Psychology, 73(1), 65–75.
Verdone, P. (1965). Temporal reference of manifest dream content. Perceptual
and Motor Skills, 20, 1253–1268.
Vogelsang, L., Anold, S., Schormann, J., Wübbelmann, S., & Schredl, M. (2016).
The continuity between waking-life musical activities and music dreams.
Dreaming, 26(2), 132–141.
220 REFERENCES
Voss, U., Holzmann, R., Tuin, I., & Hobson, J. A. (2009). Lucid dreaming: A
state of consciousness with features of both waking and non-lucid dreaming.
Sleep, 32, 1191–1200.
Voss, U., Tuin, I., Schermelleh-Engel, K., & Hobson, J. A. (2011). Waking and
dreaming: Related but structurally independent. Dream reports of congenitally
paraplegic and deaf-mute persons. Consciousness and Cognition, 20(3),
673–687.
Voss, U., Schemelleh-Engel, K., Windt, J. M., Frenzel, C., & Hobson, A. (2013).
Measuring consciousness in dreams: The lucidity and consciousness in dreams
scale. Consciousness and Cognition, 22, 8–21.
Voss, U., Holzmann, R., Hobson, A., Paulus, W., Koppehele-Gossel, J., Klimke,
A., & Nitsche, M. A. (2014). Induction of self awareness in dreams through
frontal low current stimulation of gamma activity. Nature Neuroscience, 17(6),
810–812.
Walker, M. P. (2005). A refined model of sleep and the time course of memory
formation. Behavioral and Brain Sciences, 28, 51–64.
Wamsley, E. J. (2014). Dreaming and offline memory consolidation. Current
Neurology and Neuroscience Reports, 14(3), 1–7.
Wamsley, E. J., Tucker, M., Payne, J. D., Benavides, J. A., & Stickgold, R. (2010).
Dreaming of a learning task is associated with enhanced sleep-dependent mem-
ory consolidation. Current Biology, 20, 850–855.
Wamsley, E. J., Donjacour, C. E. H. M., Scammell, T. E., Lammers, G. J., &
Stickgold, R. (2014). Delusional confusion of dreaming and reality in narco-
lepsy. Sleep: Journal of Sleep and Sleep Disorders Research, 37(2), 419–422.
Wangyal Rinpoche, T. (1998). The Tibetan yogas of dream and sleep. Ithaca: Snow
Lion.
Waterman, D. (1991). Aging and memory for dreams. Perceptual and Motor Skills,
73, 355–365.
Watson, D. (2001). Dissociations of the night: Individual differences in sleep-
related experiences and their relation to dissociation and schizotypy. Journal of
Abnormal Psychology, 110, 526–535.
Watson, D. (2003). To dream, perchance to remember: Individual differences in
dream recall. Personality and Individual Differences, 34, 1271–1286.
Wegner, D. M., Wenzlaff, R. M., & Kozak, M. (2004). Dream rebound: The
return of suppressed thoughts in dreams. Psychological Science, 15, 232–236.
Weisz, R., & Foulkes, D. (1970). Home and laboratory dreams collected under
uniform sampling conditions. Psychophysiology, 6, 588–596.
Weizsäcker, V. v. (1937). Über Träume bei sogenannter endogener Magersucht.
Deutsche Medizinsche Wochenschrift, 63, 253–257, 294–229.
Whitman, R. M., Kramer, M., & Baldridge, B. J. (1963). Which dream does the
patient tell? Archives of General Psychiatry, 8, 277–282.
REFERENCES
221
B D
Bizarreness, 67 Daydreaming, 6
Body-mind interaction, 105 Day-residue effect, 78
Brain activation, 115 Depressive disorders, 126
Dream
aggressors, 91
C definition, 1
Color in dreams, 70 deprivation, 2
Complementary hypothesis, 72 diaries, 37
Content analytic scales, 44 emotions, 52, 68
Contentless reports, 11 lag effect, 78
Continuity manual, 46
emotional, 83 questionnaire (MADRE), 67
emotional valence, 79–81 sharing, 65
formal aspects, 84 Dream content analysis, 35
hypothesis, 71, 123 statistical analyses, 53–55
self-reflective awareness, 84 Dream experiences
thematic, 82 duration, 106
M
F Meaningful stimuli, 88
Functional state-shift model, 14 Mental disorders, 123
Function(s) of REM sleep, 176 Mind wandering, 6
Mnemonic Induction of Lucid Dreams
(MILD), 165
G Mood regulation, 178
Gender differences, 89 Most recent dream approach, 36
dream recall, 18
Global rating scales, 45
N
Narcolepsy, 135
H Neuroimaging studies, 116
Hall and Van de Castle coding Nightmare
system, 46 content, 151–152
Hallucinations, 2 definition, 147
INDEX
225
S W
Salience hypothesis, 13 Wake-up-back-to-bed technique, 166
Scanning hypothesis, 109 Waking-life creativity, 66
Schizophrenia, 128 White dreaming, 11
Schredl dream manual, 47 World simulation, 2