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Benefits of Sleep Extension on Performances During Total Sleep Deprivation (BankingSleep)

NCT02352272 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2015-02-02

No results posted yet for this study

Summary

Objectives: investigate the effects of 6 nights of sleep extension on physical and cognitive performances before, during total sleep deprivation (39 hours continuous awaking) and after a subsequent recovery sleep.

Design: Subjects participated in two experimental conditions (randomized cross-over design): extended sleep (10-h in bed, EXT) and habitual sleep (8-h in bed, HAB). In each condition, subjects performed two consecutive phases: (1) six nights of either EXT or HAB (2) three experiments days in-laboratory:baseline (BASE), sleep deprivation (TSD) and after 10 h of recovery sleep(REC). Performance tests were administered every 3 hours over the 3-d in laboratory.

Setting: This cross-over and randomized study was conducted under standardized laboratory conditions with continuous polysomnographic recording Participants: 14 healthy men (age range: 26-37 years) participated in the study.

Interventions: EXT vs. HAB sleep durations prior to total sleep deprivation (39 hr continuous awaking).

Conditions

  • Sleep Deprivation

Interventions

OTHER

Total Sleep deprivation

Subject are submitted to 39 hours of continuous awaking in laboratory and a recovery night

Sponsors & Collaborators

  • Institut de Recherche Biomedicale des Armees

    lead OTHER_GOV

Principal Investigators

  • Damien LEGER, MD, PhD · Sleep center, Hotel Dieu Paris

  • Mounir CHENNAOUI, PhD · Institut de Recherche Biomedicale des Armees

  • Fabien SAUVET, MD, PhD · Institut de Recherche Biomedicale des Armees

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2014-09-30
Completion
2014-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02352272 on ClinicalTrials.gov