NCT05452733

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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 17, 2022

Completed
24 days until next milestone

First Posted

Study publicly available on registry

July 11, 2022

Completed
9 months until next milestone

Study Start

First participant enrolled

March 31, 2023

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 29, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 29, 2025

Completed
Last Updated

January 12, 2026

Status Verified

January 1, 2026

Enrollment Period

2.4 years

First QC Date

June 17, 2022

Last Update Submit

January 8, 2026

Conditions

Keywords

sleepwalkingsleepmemory consolidationreactivationdreamtargeted memory reactivation

Outcome Measures

Primary Outcomes (1)

  • Behavioral reaction

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

    2 days

Secondary Outcomes (3)

  • Evaluation of targeted memory reactivation (TMR) success in sleepwalkers by movements test

    2 days

  • Quantification of movements exhibited during sleep

    2 days

  • Determination of the link between dream and sensory cues

    2 days

Study Arms (2)

Sleepwalking patient

EXPERIMENTAL
Behavioral: differences of behavior between sleepwalking and non sleepwalking patient

Non sleepwalking patient

ACTIVE COMPARATOR
Behavioral: differences of behavior between sleepwalking and non sleepwalking patient

Interventions

movement registry done by camera when low intensity sound are send to patient during sleep.

Non sleepwalking patientSleepwalking patient

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Age between 18-35 y.o
  • Written consent
  • Affiliated to social security
  • Sleepwalking (group patients only)

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service des Pathologies du Sommeil, Hôpital Pitié-Salpétrière

Paris, Paris, 75013, France

Location

MeSH Terms

Conditions

Somnambulism

Condition Hierarchy (Ancestors)

Sleep Arousal DisordersParasomniasSleep Wake DisordersNervous System DiseasesMental Disorders

Study Officials

  • Isabelle Arnulf, MD PhD

    APHP

    PRINCIPAL INVESTIGATOR
  • Delphine Oudiette, PhD

    Institut National de la Santé Et de la Recherche Médicale, France

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 17, 2022

First Posted

July 11, 2022

Study Start

March 31, 2023

Primary Completion

August 29, 2025

Study Completion

August 29, 2025

Last Updated

January 12, 2026

Record last verified: 2026-01

Locations