SleepDance: Toward a Real-time Access to Sleepers' Mental Content

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05452733
Collaborator
Institut National de la Santé Et de la Recherche Médicale, France (Other)
200
1
2
24
8.3

Study Details

Study Description

Brief Summary

Sleep is crucial for global cognitive functioning, but its exact functions and mechanisms are still poorly understood. Cognitive studies of sleep typically rely on linking electrophysiological changes measured during sleep with behavioral and neural changes collected in tasks performed during wakefulness. What concomitantly happens in the mind of sleeping subjects is often ignored, certainly because it is virtually inaccessible. Yet, major advances in the understanding of human behaviors have resulted from an integrated approach that combines both neural and cognitive measures of their ongoing mental processes. The goal of this study is to provide real-time measures of the cognitive processes occurring within sleep.

To prompt real-time access to the sleeping mind, investigators will use auditory stimulation in people with unique sleep peculiarities: sleepwalkers whose overt behaviours may enable to objectively visualize ongoing cognitive processes during non-REM (NREM) sleep.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: differences of behavior between sleepwalking and non sleepwalking patient
N/A

Detailed Description

Investigators aim to offer a quantifiable, real-time measure of memory processing during NREM sleep by using memory-related cues to influence which behaviours sleepwalkers will exhibit. Because sleepwalking is characterized by complex behaviors emerging from NREM sleep, it could provide an observable window into mental activity in NREM sleep. While neuronal memory reactivations have largely been demonstrated in sleeping rodents, evidence for the existence of such reactivations in humans is at best indirect. Here, investigators will use targeted memory reactivation (TMR), a tool that allows to control which individual memories are reactivated on a trial by trial basis. TMR consists in associating sensory cues with a specific learning, then re-applying these cues during subsequent sleep to trigger the reactivation of the corresponding learning. Sleepwalkers will be trained on a modified version of the serial reaction time task: sleepwalkers will perform as fast and accurately as possible a sequence of gestures in response to auditory cues. Investigators goals are to: i) show that playing the auditory cues during NREM sleep triggers a behavioral replay of the learned 'choreography' in sleepwalkers, ii) quantify, with a gesture recognition algorithm, how the sleep gestures differ from the wake ones (speed, accuracy, sequence fidelity), and

  1. test whether this evoked replay is accompanied by a congruent dream.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Toward a Real-time Access to Sleepers' Mental Content
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Sep 30, 2024
Anticipated Study Completion Date :
Sep 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Sleepwalking patient

Behavioral: differences of behavior between sleepwalking and non sleepwalking patient
movement registry done by camera when low intensity sound are send to patient during sleep.

Active Comparator: Non sleepwalking patient

Behavioral: differences of behavior between sleepwalking and non sleepwalking patient
movement registry done by camera when low intensity sound are send to patient during sleep.

Outcome Measures

Primary Outcome Measures

  1. Behavioral reaction [2 days]

    number of behavioral reactivations of the motor sequence following the auditory cues during sleep

Secondary Outcome Measures

  1. Evaluation of targeted memory reactivation (TMR) success in sleepwalkers by movements test [2 days]

    test whether performance is better for movements that have been cued during sleep (vs. uncued ones) in sleepwalkers

  2. Quantification of movements exhibited during sleep [2 days]

    The quantification of movement will be evaluated by combinaison of the reaction time, speed and precision of movements exhibited by sleepwalkers during sleep vs. wakefulness

  3. Determination of the link between dream and sensory cues [2 days]

    Comparison between the number of dreams related to the motor sequence on the 2nd night (after TMR) vs. during the 1st one.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age between 18-35 y.o

  • Written consent

  • Affiliated to social security

  • Sleepwalking (group patients only)

Exclusion Criteria:
  • Psychiatric or neurologic disorder

  • Sleep disorder except sleepwalking for the patient group

  • Surdity

  • Pain or physical disability affecting the upper limbs

  • Consumption of drugs altering sleep structure

  • Subjects under legal protection

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service des Pathologies du Sommeil, Hôpital Pitié-Salpétrière Paris France 75013

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris
  • Institut National de la Santé Et de la Recherche Médicale, France

Investigators

  • Principal Investigator: Isabelle Arnulf, MD PhD, APHP
  • Study Director: Delphine Oudiette, PhD, Institut National de la Santé Et de la Recherche Médicale, France

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT05452733
Other Study ID Numbers:
  • APHP XX
First Posted:
Jul 11, 2022
Last Update Posted:
Jul 11, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 11, 2022