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

Primary Purpose

Memory Reactivation, Memory Consolidation, Sleepwalking

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
differences of behavior between sleepwalking and non sleepwalking patient
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Memory Reactivation focused on measuring sleepwalking, sleep, memory consolidation, reactivation, dream, targeted memory reactivation

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Service des Pathologies du Sommeil, Hôpital Pitié-SalpétrièreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sleepwalking patient

Non sleepwalking patient

Arm Description

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Evaluation of targeted memory reactivation (TMR) success in sleepwalkers by movements test
test whether performance is better for movements that have been cued during sleep (vs. uncued ones) in sleepwalkers
Quantification of movements exhibited during sleep
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
Determination of the link between dream and sensory cues
Comparison between the number of dreams related to the motor sequence on the 2nd night (after TMR) vs. during the 1st one.

Full Information

First Posted
June 17, 2022
Last Updated
May 5, 2023
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France
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1. Study Identification

Unique Protocol Identification Number
NCT05452733
Brief Title
Toward a Real-time Access to Sleepers' Mental Content
Acronym
SleepDance
Official Title
Toward a Real-time Access to Sleepers' Mental Content
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 31, 2023 (Actual)
Primary Completion Date
March 30, 2025 (Anticipated)
Study Completion Date
March 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. 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.
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 iii) test whether this evoked replay is accompanied by a congruent dream.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Memory Reactivation, Memory Consolidation, Sleepwalking
Keywords
sleepwalking, sleep, memory consolidation, reactivation, dream, targeted memory reactivation

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sleepwalking patient
Arm Type
Experimental
Arm Title
Non sleepwalking patient
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
differences of behavior between sleepwalking and non sleepwalking patient
Intervention Description
movement registry done by camera when low intensity sound are send to patient during sleep.
Primary Outcome Measure Information:
Title
Behavioral reaction
Description
number of behavioral reactivations of the motor sequence following the auditory cues during sleep
Time Frame
2 days
Secondary Outcome Measure Information:
Title
Evaluation of targeted memory reactivation (TMR) success in sleepwalkers by movements test
Description
test whether performance is better for movements that have been cued during sleep (vs. uncued ones) in sleepwalkers
Time Frame
2 days
Title
Quantification of movements exhibited during sleep
Description
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
Time Frame
2 days
Title
Determination of the link between dream and sensory cues
Description
Comparison between the number of dreams related to the motor sequence on the 2nd night (after TMR) vs. during the 1st one.
Time Frame
2 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Isabelle Arnulf, MD PhD
Phone
01 42 16 77 04
Email
Isabelle.arnulf@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Delphine Oudiette, PhD
Phone
01 42 16 77 16
Email
delphine.oudiette-ext@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isabelle Arnulf, MD PhD
Organizational Affiliation
APHP
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Delphine Oudiette, PhD
Organizational Affiliation
Institut National de la Santé Et de la Recherche Médicale, France
Official's Role
Study Director
Facility Information:
Facility Name
Service des Pathologies du Sommeil, Hôpital Pitié-Salpétrière
City
Paris
ZIP/Postal Code
75013
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Isabelle Arnulf, MD, PhD
Phone
01 42 16 77 04
Email
Isabelle.arnulf@aphp.fr
First Name & Middle Initial & Last Name & Degree
Delphine Oudiette, PhD
Phone
01 42 16 77 16
Email
delphine.oudiette-ext@aphp.fr

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Toward a Real-time Access to Sleepers' Mental Content

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