Lucid dreaming: a state of consciousness with features of both waking and non-lucid dreaming
Open accessAbstract
STUDY OBJECTIVES: The goal of the study was to seek physiological correlates of lucid dreaming. Lucid dreaming is a dissociated state with aspects of waking and dreaming combined in a way so as to suggest a specific alteration in brain physiology for which we now present preliminary but intriguing evidence. We show that the unusual combination of hallucinatory dream activity and wake-like reflective awareness and agentive control experienced in lucid dreams is paralleled by significant changes in electrophysiology. DESIGN: 19-channel EEG was recorded on up to 5 nights for each participant. Lucid episodes occurred as a result of pre-sleep autosuggestion. SETTING: Sleep laboratory of the Neurological Clinic, Frankfurt University. PARTICIPANTS: Six student volunteers who had been trained to become lucid and to signal lucidity through a pattern of horizontal eye movements. MEASUREMENTS AND RESULTS: Results show lucid dreaming to have REM-like power in frequency bands delta and theta, and higher-than-REM activity in the gamma band, the between-states-difference peaking around 40 Hz. Power in the 40 Hz band is strongest in the frontal and frontolateral region. Overall coherence levels are similar in waking and lucid dreaming and significantly higher than in REM sleep, throughout the entire frequency spectrum analyzed. Regarding specific frequency bands, waking is characterized by high coherence in alpha, and lucid dreaming by increased delta and theta band coherence. In lucid dreaming, coherence is largest in frontolateral and frontal areas. CONCLUSIONS: Our data show that lucid dreaming constitutes a hybrid state of consciousness with definable and measurable differences from waking and from REM sleep, particularly in frontal areas.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Lucid dreaming is associated with further increased gamma activity and coherence in the dorsolateral prefrontal cortex relative to REM sleep, approaching waking levels.
“Lucid dreaming is associated with further increased gamma activity and coherence in the dorsolateral prefrontal cortex relative to REM sleep, approaching levels consistent with waking (Voss et al., 2009).”
From Conscious Processing and the Global Neuronal Workspace Hypothesis (2020) · cites this paper as Voss et al., 2009
The Abstract reports higher-than-REM gamma activity in lucid dreaming, strongest in frontal and frontolateral regions, and overall coherence similar to waking and higher than REM. But the regional differences section says the EEG data cannot test whether the dorsolateral prefrontal cortex is reactivated, and it does not establish a gamma-specific coherence increase there. (LLM, conf=0.91)
Experimental — accuracy not yet measuredBecause lucid dreaming is considered a hybrid of REM sleep and waking, studies showing a causal role for the prefrontal cortex in lucid dreaming support a role for the prefrontal cortex in waking consciousness.
“Given that lucid dreaming is considered a hybrid of REM sleep and waking (Voss et al., 2009), studies demonstrating a causal role for the prefrontal cortex in lucid dreaming thus also support a role for the prefrontal cortex in waking consciousness.”
From Conscious Processing and the Global Neuronal Workspace Hypothesis (2020) · cites this paper as Voss et al., 2009
Emergence of the observing self is associated with frontal lobe activation.
“Emergence of the observing self is associated with frontal lobe activation (Voss et al., 2009), a fact that accords well with executive functions attributed to this region.”
From Virtual reality and consciousness inference in dreaming (2014) · cites this paper as Voss et al., 2009
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Rechtschaffen, A. (1968) · Medical Entomology and Zoology · Cited by 11,772 · see citing works
A new method for off-line removal of ocular artifact
Gratton, G., Coles, M. G. H., & Donchin, E. (1983) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(83)90135-9 · Cited by 5,055 · see citing works
The brainweb: phase synchronization and large-scale integration
Varela, F., Lachaux, J.-P., Rodriguez, E., & Martinerie, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35067550 · Cited by 4,761 · see citing works
Nunez, P. L., & Srinivasan, R. (2006) · doi:10.1093/acprof:oso/9780195050387.001.0001 · Cited by 2,531 · see citing works
Electric Fields of the Brain: The Neurophysics of EEG
Nunez, P. L., & Harth, E. M. (1982) · Physics Today · doi:10.1063/1.2915137 · Cited by 2,257 · see citing works
Conscious, preconscious, and subliminal processing: a testable taxonomy
Dehaene, S., Changeux, J.-P., Naccache, L., Sackur, J., & Sergent, C. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.03.007 · Cited by 2,067 · see citing works
Perception's shadow: long-distance synchronization of human brain activity
Rodriguez, E., George, N., Lachaux, J.-P., Martinerie, J., Renault, B., & Varela, F. J. (1999) · Nature · doi:10.1038/17120 · Cited by 1,915 · see citing works
Electric Fields of the Brain: The Neurophysics of EEG
Fermaglich, J. (1982) · JAMA · doi:10.1001/jama.1982.03320380071046 · Cited by 1,557 · see citing works
Nunez, P. L., Srinivasan, R., Westdorp, A. F., Wijesinghe, R. S., Tucker, D. M., Silberstein, R. B., & Cadusch, P. J. (1997) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/s0013-4694(97)00066-7 · Cited by 1,230 · see citing works
Functional neuroanatomy of human rapid-eye-movement sleep and dreaming
Maquet, P., Péters, J.-M., Aerts, J., Delfiore, G., Degueldre, C., Luxen, A., & Franck, G. (1996) · Nature · doi:10.1038/383163a0 · Cited by 1,168 · see citing works
Fries, P., Nikolić, D., & Singer, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.05.005 · Cited by 1,044 · see citing works
An on-line transformation of EEG scalp potentials into orthogonal source derivations
Hjorth, B. (1975) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(75)90056-5 · Cited by 1,014 · see citing works
Dreaming and the brain: toward a cognitive neuroscience of conscious states
Hobson, J. A., Pace-Schott, E. F., & Stickgold, R. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00003976 · Cited by 985 · see citing works
Coherence of gamma-band EEG activity as a basis for associative learning
Miltner, W. H. R., Braun, C., Arnold, M., Witte, H., & Taub, E. (1999) · Nature · doi:10.1038/17126 · Cited by 798 · see citing works
Transient induced gamma-band response in EEG as a manifestation of miniature saccades
Yuval-Greenberg, S., Tomer, O., Keren, A. S., Nelken, I., & Deouell, L. Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.027 · Cited by 776 · see citing works
Synchronization of neural activity across cortical areas correlates with conscious perception
Melloni, L., Molina, C., Pena, M., Torres, D., Singer, W., & Rodriguez, E. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4623-06.2007 · Cited by 716 · see citing works
The prefrontal cortex in sleep
Muzur, A., Pace-Schott, E. F., & Hobson, J. A. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)01992-7 · Cited by 571 · see citing works
Srinivasan, R., Winter, W., Ding, J., & Nunez, P. L. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.06.026 · Cited by 538 · see citing works
Whitham, E. M., Pope, K. J., Fitzgibbon, S. P., Lewis, T., Clark, C. R., Loveless, S., Broberg, M., Wallace, A., DeLosAngeles, D., Lillie, P., et al. (2007) · Clinical Neurophysiology · doi:10.1016/j.clinph.2007.04.027 · Cited by 524 · see citing works
Forebrain activation in REM sleep: an FDG PET study
Nofzinger, E. A., Mintun, M. A., Wiseman, M., Kupfer, D. J., & Moore, R. Y. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00807-x · Cited by 501 · see citing works
Consciousness and the Binding Problem
SINGER, W. (2001) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2001.tb05712.x · Cited by 367 · see citing works
EEG coherency II: experimental comparisons of multiple measures
Nunez, P. L., Silberstein, R. B., Shi, Z., Carpenter, M. R., Srinivasan, R., Tucker, D. M., Doran, S. M., Cadusch, P. J., & Wijesinghe, R. S. (1999) · Clinical Neurophysiology · doi:10.1016/s1388-2457(98)00043-1 · Cited by 316 · see citing works
Kayser, J., & Tenke, C. E. (2005) · Clinical Neurophysiology · doi:10.1016/j.clinph.2005.08.033 · Cited by 292 · see citing works
Thinking activates EMG in scalp electrical recordings
Whitham, E. M., Lewis, T. W., Pope, K. J., Fitzgibbon, S. P., Clark, C. R., Loveless, S., DeLosAngeles, D., Wallace, A. K., Broberg, M., & Willoughby, J. O. (2008) · Clinical Neurophysiology · doi:10.1016/j.clinph.2008.01.024 · Cited by 167 · see citing works
Singer, W. (1999) · Nature · doi:10.1038/17021 · Cited by 162 · see citing works
Gamma EEG dynamics in neocortex and hippocampus during human wakefulness and sleep
Cantero, J. L., Atienza, M., Madsen, J. R., & Stickgold, R. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.03.014 · Cited by 143 · see citing works
Winter, W., Nunez, P. L., Ding, J., & Srinivasan, R. (2007) · Statistics in Medicine · doi:10.1002/sim.2978 · Cited by 121 · see citing works
Lucid dreaming: Physiological correlates of consciousness during Rem sleep
LaBerge, S. P., Levitan, L., & Dement, W. C. (1986) · The Journal of mind and behavior · Cited by 100 · see citing works
Trujillo, L. T., Peterson, M. A., Kaszniak, A. W., & Allen, J. J. B. (2004) · Clinical Neurophysiology · doi:10.1016/j.clinph.2004.07.025 · Cited by 98 · see citing works
Methods to improve spatial resolution of EEG
Nunez, P. L. (1988) · Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society · doi:10.1109/iembs.1988.95290 · Cited by 84 · see citing works
Psychophysiological correlates of lucid dreaming.
Holzinger, B., LaBerge, S. P., & Levitan, L. (2006) · Dreaming · doi:10.1037/1053-0797.16.2.88 · Cited by 70 · see citing works
Wider than the sky : a revolutionary view of consciousness
Edelman, G. M. (2005) · Penguin Books · Cited by 55 · see citing works
Lagerlund, T. D., Sharbrough, F. W., Busacker, N. E., et al. (1995) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(95)00025-t · Cited by 39 · see citing works
Rhinal–hippocampal EEG coherence is reduced during human sleep
Fell, J., Staedtgen, M., Burr, W., Kockelmann, E., Helmstaedter, C., Schaller, C., Elger, C. E., & Fernández, G. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02934.x · Cited by 38 · see citing works
Directional tuning of the human presaccadic spike potential
Weinstein, J. M., Balaban, C. D., & VerHoeve, J. N. (1991) · Brain Research · doi:10.1016/0006-8993(91)90034-s · Cited by 23 · see citing works
Arnold-Forster, M. (1921) · Cited by 17 · see citing works
[Two treatises on Greek mythology].
Borkenau, F. (1957) · PubMed · Cited by 10 · see citing works
Finally some one: Reflections on Thomas Metzinger's Being No One
Hobson, A. J. (2005) · Cited by 2 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 3
- [27]27. Nunez PL, Srinivasan R, Westdorp AF, et al. EEG coherence I: 10. statistics, reference electrode, volume conduction, Laplacians, cortical imaging, and interpretation at multiple scales. Electroen- ceph Clin Neurophysiol 1997;103:499-515.
- [28]28. Nunez PL, Silberstein RB, Shi ZP, et al. EEG coherence II: ex- 11. perimental comparisons of multiple measures. Clin Neurophysiol 1999;110:469-86.
- [33]33. Hjorth B. Online transformation of EEG scalp potentials into or- 16. thogonal source derivations. Electroenceph Clin Neurophysiol 1975;39:526-30.
Cited by
Sorted by citations
Conscious Processing and the Global Neuronal Workspace Hypothesis
Mashour, G. A., Roelfsema, P., Changeux, J.-P., & Dehaene, S. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.026 · Cited by 1,164 · see citing works
“Given that lucid dreaming is considered a hybrid of REM sleep and waking (Voss et al., 2009), studies demonstrating a causal role for the PFC in lucid dreaming thus also support a role for the PFC in waking consciousness.”
BackgroundThe neural correlates of dreaming
Siclari, F., Baird, B., Perogamvros, L., Bernardi, G., LaRocque, J. J., Riedner, B., Boly, M., Postle, B. R., & Tononi, G. (2017) · Nature Neuroscience · doi:10.1038/nn.4545 · Cited by 712 · see citing works
REM sleep and dreaming: towards a theory of protoconsciousness
Hobson, J. A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2716 · Cited by 625 · see citing works
Unresponsiveness ≠ unconsciousness
Sanders, R. D., Tononi, G., Laureys, S., Sleigh, J. W., & Warner, D. S. (2012) · Anesthesiology · doi:10.1097/aln.0b013e318249d0a7 · Cited by 474 · see citing works
Induction of self awareness in dreams through frontal low current stimulation of gamma activity
Voss, U., Holzmann, R., Hobson, A., Paulus, W., Koppehele-Gossel, J., Klimke, A., & Nitsche, M. A. (2014) · Nature Neuroscience · doi:10.1038/nn.3719 · Cited by 340 · see citing works
Self-citationConsciousness in humans and non-human animals: recent advances and future directions
Boly, M., Seth, A. K., Wilke, M., Ingmundson, P., Baars, B., Laureys, S., Edelman, D. B., & Tsuchiya, N. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00625 · Cited by 291 · see citing works
Dresler, M., Wehrle, R., Spoormaker, V. I., Koch, S. P., Holsboer, F., Steiger, A., Obrig, H., Sämann, P. G., & Czisch, M. (2012) · Sleep · doi:10.5665/sleep.1974 · Cited by 271 · see citing works
Sleep disturbance as a universal risk factor for relapse in addictions to psychoactive substances
Brower, K. J., & Perron, B. E. (2010) · Medical Hypotheses · doi:10.1016/j.mehy.2009.10.020 · Cited by 226 · see citing works
Virtual reality and consciousness inference in dreaming
Hobson, J. A., Hong, C. C.-H., & Friston, K. J. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.01133 · Cited by 197 · see citing works
“Emergence of the observing self is associated with frontal lobe activation (Voss et al., 2009), a fact that accords well with executive functions attributed to this region.”
BackgroundMarshall, L., Kirov, R., Brade, J., Mölle, M., & Born, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016905 · Cited by 188 · see citing works
The cognitive neuroscience of lucid dreaming
Baird, B., Mota-Rolim, S. A., & Dresler, M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.03.008 · Cited by 192 · see citing works
Cognitive and emotional processes during dreaming: a neuroimaging view
Desseilles, M., Dang-Vu, T. T., Sterpenich, V., & Schwartz, S. (2011) · Consciousness and Cognition · doi:10.1016/j.concog.2010.10.005 · Cited by 182 · see citing works
Dreamed movement elicits activation in the sensorimotor cortex
Dresler, M., Koch, S. P., Wehrle, R., Spoormaker, V. I., Holsboer, F., Steiger, A., Sämann, P. G., Obrig, H., & Czisch, M. (2011) · Current Biology · doi:10.1016/j.cub.2011.09.029 · Cited by 168 · see citing works
The vigilant sleeper: neural mechanisms of sensory (de)coupling during sleep
Andrillon, T., & Kouider, S. (2020) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.12.002 · Cited by 133 · see citing works
Dodet, P., Chavez, M., Leu-Semenescu, S., Golmard, J.-L., & Arnulf, I. (2015) · SLEEP · doi:10.5665/sleep.4516 · Cited by 118 · see citing works
Acute biphasic effects of ayahuasca.
Schenberg, E. E., Alexandre, J. F. M., Filev, R., Cravo, A. M., Sato, J. R., Muthukumaraswamy, S. D., Yonamine, M., Waguespack, M., Lomnicka, I., Barker, S. A., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0137202 · Cited by 111 · see citing works
Dreams and nightmares in healthy adults and in patients with sleep and neurological disorders
Siclari, F., Valli, K., & Arnulf, I. (2020) · The Lancet Neurology · doi:10.1016/s1474-4422(20)30275-1 · Cited by 98 · see citing works
Dreams and Psychedelics: Neurophenomenological Comparison and Therapeutic Implications
Kraehenmann, R. (2017) · Current Neuropharmacology · doi:10.2174/1573413713666170619092629 · Cited by 92 · see citing works
Testing the involvement of the prefrontal cortex in lucid dreaming: a tDCS study
Stumbrys, T., Erlacher, D., & Schredl, M. (2013) · Consciousness and Cognition · doi:10.1016/j.concog.2013.08.005 · Cited by 85 · see citing works
Lucid dreaming: an age-dependent brain dissociation.
VOSS, U., FRENZEL, C., KOPPEHELE‐GOSSEL, J., & HOBSON, A. (2012) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2012.01022.x · Cited by 76 · see citing works
Self-citationDenis, D., & Poerio, G. L. (2017) · Journal of Sleep Research · doi:10.1111/jsr.12441 · Cited by 70 · see citing works
Dreaming as a story-telling instinct
Pace-Schott, E. F. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00159 · Cited by 69 · see citing works
Does metarepresentation make human mental time travel unique?
Redshaw, J. (2014) · WIREs Cognitive Science · doi:10.1002/wcs.1308 · Cited by 68 · see citing works
Cipolli, C., Ferrara, M., De Gennaro, L., & Plazzi, G. (2017) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2016.07.005 · Cited by 67 · see citing works
Studies with lucid dreaming as add-on therapy to Gestalt therapy
Holzinger, B., Klösch, G., & Saletu, B. (2015) · Acta Neurologica Scandinavica · doi:10.1111/ane.12362 · Cited by 61 · see citing works
Coherent neocortical 40‐Hz oscillations are not present during <scp>REM</scp> sleep
Castro, S., Falconi, A., Chase, M. H., & Torterolo, P. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12143 · Cited by 54 · see citing works
Increased lucid dreaming frequency in narcolepsy
Rak, M., Beitinger, P., Steiger, A., Schredl, M., & Dresler, M. (2015) · SLEEP · doi:10.5665/sleep.4676 · Cited by 58 · see citing works
Relationships between sleep paralysis and sleep quality: current insights
Denis, D. (2018) · Nature and Science of Sleep · doi:10.2147/nss.s158600 · Cited by 59 · see citing works
Türker, B., Musat, E. M., Chabani, E., Fonteix-Galet, A., Maranci, J.-B., Wattiez, N., Pouget, P., Sitt, J., Naccache, L., Arnulf, I., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01449-7 · Cited by 57 · see citing works
Volitional components of consciousness vary across wakefulness, dreaming and lucid dreaming
Dresler, M., Eibl, L., Fischer, C. F. J., Wehrle, R., Spoormaker, V. I., Steiger, A., Czisch, M., & Pawlowski, M. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00987 · Cited by 52 · see citing works
Alpha reactivity to first names differs in subjects with high and low dream recall frequency
Ruby, P., Blochet, C., Eichenlaub, J.-B., Bertrand, O., Morlet, D., & Bidet-Caulet, A. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00419 · Cited by 44 · see citing works
Lucid dreaming occurs in activated rapid eye movement sleep, not a mixture of sleep and wakefulness
Baird, B., Tononi, G., & LaBerge, S. (2022) · Sleep · doi:10.1093/sleep/zsab294 · Cited by 41 · see citing works
Sleep Paralysis in Brazilian Folklore and Other Cultures: A Brief Review
de Sá, J. F. R., & Mota-Rolim, S. A. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.01294 · Cited by 39 · see citing works
Why Does Rem Sleep Occur? A Wake-Up Hypothesis1
Klemm, W. R. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00073 · Cited by 27 · see citing works
Siclari, F., & Tononi, G. (2016) · The Neurology of Conciousness · doi:10.1016/b978-0-12-800948-2.00007-8 · Cited by 27 · see citing works
A beautiful loop: An active inference theory of consciousness.
Laukkonen, R., Friston, K., & Chandaria, S. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106296 · Cited by 22 · see citing works
“A growing evidence base suggests that active inference is, or at least could be, what the brain and body are doing (Walsh et al., 2020; Hohwy, 2013).”
Llewellyn, S. (2016) · Consciousness and Cognition · doi:10.1016/j.concog.2016.09.018 · Cited by 17 · see citing works
Ableidinger, S., & Holzinger, B. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12103437 · Cited by 13 · see citing works
To what extent do neurobiological sleep-waking processes support psychoanalysis?
Gottesmann, C. (2010) · International review of neurobiology · doi:10.1016/s0074-7742(10)92012-6 · Cited by 5 · see citing works
- Authors
- Voss, U., Holzmann, R., Tuin, I., & Hobson, A. J.
- Affiliations
- Goethe University Frankfurt (DE)
- GSI Helmholtz Centre for Heavy Ion Research (DE)
- Johannes Gutenberg University Mainz (DE)
- Beth Israel Deaconess Medical Center (US)
- Corresponding author
- Voss, Ursula
- Venue
- Sleep
- Publisher
- Oxford University Press (OUP)
- Published
- 2009-09
- Volume
- 32
- Issue
- 9
- Pages
- 1191-1200
- ISSN
- 0161-8105 (ISSN-L)
- 1550-9109
- PMC
- PMC2737577
- OpenAlex
- W1693689577
- Cited by
- 445
- References
- 38
- Citations by year
- 2026: 15 · 2025: 39 · 2024: 20 · 2023: 23 · 2022: 33 · 2021: 28 · 2020: 34 · 2019: 23 · 2018: 27 · 2017: 26 · 2016: 30 · 2015: 30 · 2014: 30 · 2013: 31 · 2012: 16
- FWCI
- 9.03
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- SLEEP (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Social Sciences › Psychology › Social Psychology › Paranormal Experiences and Beliefs
- Keywords
- lucid dreaming, REM sleep, EEG coherence, EEG spectral power, gamma band, delta band, theta band, frontal lobe activity, alpha band
- MeSH terms
- Awareness, Brain, Brain Mapping, Consciousness, Dreams, Electroencephalography, Female, Germany, Humans, Male, Sleep, REM, Students, Time Factors, Wakefulness, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review