Trial Radar AI | ||
|---|---|---|
De klinische studie NCT07408206 voor angst is rekruterend. Bekijk de kaartweergave van de Klinische Studies Radar en de AI-ontdekkingstools voor alle details. Of stel hier een vraag. | ||
Eén studie komt overeen met de filtercriteria
Kaartweergave
Sleep, Dreaming, and Virtual Reality for Mental Health Vroege fase 1 70 Gerandomiseerd Virtueel
Informatie over klinische studies is voornamelijk in het Engels beschikbaar. Trial Radar AI kan echter helpen! Klik op 'Leg studie uit' om de informatie over de studie te bekijken en te bespreken in de taal van uw keuze.
De klinische studie NCT07408206 onderzoekt behandeling bij angst. Deze Vroege fase 1 interventioneel-studie heeft de status rekruterend. Het doel is om 70 deelnemers te includeren vanaf 15 januari 2026. De studie wordt geleid door Northwestern-universiteit en de voltooiing is gepland op 31 december 2027. Laatste update op ClinicalTrials.gov: 18 februari 2026.
Beknopte samenvatting
People spend approximately one-third of their lives asleep, yet sleep is often underused as an opportunity to support psychological well-being. Contemplative traditions, including Tibetan Dream Yoga, have developed practices that use waking imagination and lucid dreaming to explore perception, awareness, and habitual patterns of thinking. Recent advances in sleep monitoring, dream communication, and lucid dream induc...Toon meer
Uitgebreide beschrijving
Dream Yoga is a contemplative practice with a documented history spanning more than a millennium, described in traditional manuals as a set of waking and sleep-based exercises intended to cultivate insight, perceptual flexibility, and altered self-referential processing. These practices include the intentional induction of lucid dreaming, in which individuals become aware that they are dreaming and may exert varying ...Toon meer
Officiële titel
Transformative Benefits of Contemplative Sleep Practices and a Novel Pathway to Deliver Benefits to the General Public
Aandoeningen
angstAndere studie-ID's
- STU00222189-MOD0004
NCT-ID
Startdatum (Werkelijk)
2026-01-15
Laatste update geplaatst
2026-02-18
Verwachte einddatum
2027-12-31
Inschrijving (Geschat)
70
Studietype
Interventioneel
FASE
Vroege fase 1
Status
Rekruterend
Trefwoorden
lucid dreaming
dream yoga
contemplative practices
meditation
mind-body interventions
dream yoga
contemplative practices
meditation
mind-body interventions
Primaire doel
Behandeling
Toewijzing
Gerandomiseerd
Interventiemodel
Parallel
Blindering
Dubbelblind
Armen / Interventies
| Deelnemersgroep/Studiearm | Interventie/Behandeling |
|---|---|
ExperimenteelDream Yoga Inspired Intervention This customized contemplative training will guide participants in exploring techniques used in Tibetan Dream Yoga. Strategies in Tibetan Dream-Yoga manuals are thus transferred to a modern context and adapted as a group intervention. Goals will be set for dreaming that include gaining a degree of volitional influence over the dream. Wearable devices will be used to present cues during sleep both to provoke lucidity a...Toon meer | Dream Yoga Inspired Intervention This customized contemplative training will guide participants in exploring techniques used in Tibetan Dream Yoga. Strategies in Tibetan manuals are thus transferred to a modern context and adapted as a group intervention. Goals will be set for dreaming that include gaining lucidity, a degree of volitional influence over the dream. Participants will be instructed on how to work with their dream-world self-concept, wh...Toon meer |
Actieve comparatorSleep Health Enhancement program A modified version of the Health Enhancement Program (HEP), which was developed as an active control condition for mindfulness-based interventions, with a particular focus on sleep hygiene. It controls for several non-specific factors such as expectations of positive change, group support, behavioural activation, facilitator attention, at-home practice, treatment duration, and format (MacCoon et al., 2012; Rosenkranz...Toon meer | Sleep Health Enhancement Program (SHEP) The control group will receive a modified version of the Health Enhancement Program (HEP), which was developed as an active control condition for mindfulness-based interventions, with a particular focus on sleep hygiene and dream journaling. It controls for several non-specific factors such as expectations of positive change, group support, behavioural activation, facilitator attention, at-home practice, treatment du...Toon meer |
Primaire uitkomst
Secundaire uitkomst
| Uitkomstmaat | Beschrijving van de uitkomstmaat | Tijdsbestek |
|---|---|---|
Changes in frontal midline theta | The intervention will preferentially increase frontal midline theta during a short period of breath meditation (one recording session before and one after the intervention); EEG power band-passed at 4-10 Hz will be quantified and related to findings on self-referential processing (Nondual Awareness Dimensional Assessment) | Baseline to 8 weeks |
Changes in Sleep Architecture | Sleep architecture will be compared with regard to time spent in each sleep stage, microarousals, slow-wave power, sleep spindles, and coupling between slow waves and spindles. Spectral power differences in different sleep stages. | Baseline and 8 weeks |
| Uitkomstmaat | Beschrijving van de uitkomstmaat | Tijdsbestek |
|---|---|---|
Changes in Lucid Dreaming Frequency | Lucidity will be assessed with a composite of questionnaires at week 1 and measuring changes at week 8 and using self-reports of lucid dreams recorded in daily dream journals and/or nightly reports during the 7-week intervention.Additionally participants will fill tge Self-report Questionnaires: 1. Lucid Dreaming Skills Questionnaire (LUSK) 2. Lucid Dream Control-Specific Experiences (LDC-SE) | Baseline to 8 weeks |
Changes in Cognitive Flexibility - Cognitive Flexibility Scale | Several facets of cognitive flexibility will be measured with the Cognitive Flexibility Scale | Baseline to 8 weeks |
Changes in Cognitive Flexibility - Probabilistic Reversal | Several facets of cognitive flexibility will be measured with several standard neuropsychological tests such as the Probabilistic Reversal Learning. | Baseline to 8 weeks |
Changes in Cognitive Flexibility - Stroop Test | Several facets of cognitive flexibility will be measured with standard neuropsychological tests such as the Stroop color-word test, Emotional Stroop. | Baseline to 8 weeks |
Deelname-assistent
Geschiktheidscriteria
Leeftijd van deelnemers
Volwassene, Oudere volwassene
Minimumleeftijd
18 Years
Geslachten die in aanmerking komen voor de studie
Allen
Accepteert gezonde vrijwilligers
Ja
- Individuals interested in participating will be screened for eligibility through a Qualtrics survey, a Score between 5-21 points in GAD-7.
Healthy, English-speaking adults (at least 18 years old) with high dream recall (at least 1/week).
We will exclude people who self-report any of the following:
- history of an established meditative practice
- psychological or psychiatric disorders (other than mild anxiety)
- sleep disorders, nightshift work in the past month, extreme chronotype or irregular sleeping pattern
- use of recreational drugs in the past month
- history of asthma, seizures or heart problems
- unwillingness to wear headband during sleep
Verantwoordelijke instantie
Ken Paller, Hoofdonderzoeker, Professor, Northwestern University
Centraal Contactpersoon
Contact: S. Gabriela Torres Platas, Ph.D., (847) 491-3741, [email protected]
2 Studielocaties in 1 landen
Illinois
Northwestern University, Evanston, Illinois, 60208, United States
Susan Florczak, Contact, 847-491-3741, [email protected]
Rekruterend
Virginia
Contemplative Sciences Center, Charlottesville, Virginia, 22903-2628, United States
Michael Sheehy, Ph.D, Contact, (434) 982-6057, [email protected]
Contact, [email protected]
S. Gabriela Torres Platas, Ph.D., Hoofdonderzoeker
Rekruterend