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

January 27, 2015 updated by: Fabien SAUVET, Institut de Recherche Biomedicale des Armees

Benefits of Sleep Extension on Cognitive and Physical Performances During Baseline, Total Sleep Deprivation and Recovery (BankingSleep)

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).

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Many human endeavors require high-level cognitive performance situations (e.g., health care, military operations, space flight) along the whole nycthemera (i.e. the 24-h cycle).

It has long been established that both acute total sleep deprivation (TSD) and chronic sleep restriction impair ability to maintain wakefulness, increase subjective sleepiness and sleep propensity, and most critically reduce various aspects of cognitive performance. In studies conducted in both laboratory setting and different professional situations inducing insufficient sleep, the most consistently and dramatically impacted cognitive capacities were sustained attention and alertness. This degradation of cognitive performance after a period of sleep deprivation is linked to an increase of sleep pressure, e.g. a reduction in the latency to sleep onset or increase of number of involuntary micro sleeps.

To identify countermeasures to deleterious effects of sleep deprivation is critical in many professional areas.

Management of wake/sleep cycle appears to have an important impact of alertness during sleep deprivation (e.g. sleep habits or physical activity, see the review. Recently, Rupp and coll. (2012) reported that one week of sleep extension realized before one week of sleep restriction (3 h/night) influence the rate of degradation of cognitive performance and alertness during this period and the subsequent recovery period. In other words, they proposed that sleep can be "banked" before a period of sleep loss and may help sustain performance and alertness. With a different experimental paradigm (i.e. without subsequent sleep deprivation), studies have shown that sleep extension (realized over different periods of time) may improve physical performance, attentional performance, or mood. The fact of increasing total sleep time over a period of time represents an attractive non-pharmacological countermeasure to limit the deleterious effects on performance induced by sleep privation. However, there is no study with cross-over and randomized design to assess effect on relatively short period (6 nights) of sleep extension on performance before, during total sleep deprivation and recovery. Moreover, there is no direct measurement of sleep pressure as continuous EEG monitoring to quantify micro sleep episode during period of sleep deprivation and effect of sleep extension on physical performance is not known.

Hence, the aim of this study was to assess the effects of 6 nights of sleep extension (EXT) on physical and cognitive performances, alertness and homeostatic sleep pressure before, during total sleep deprivation and the subsequent recovery day.

The investigators hypothesized that EXT would: i) partly prevents the physical and cognitive performances degradation-induced by total sleep deprivation ii) decreases the sleep pressure before, during and after total sleep deprivation and iii) improves the recovery speed of physical and cognitive performances.

Study Type

Interventional

Enrollment (Actual)

14

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Paris, France, 75003
        • Hotel Dieu Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • healthy subject
  • voluntary

Exclusion Criteria:

  • an average of > 9 h and < 6 h sleep per night
  • a difference > 45 min between week night and weekend night
  • sleep debt
  • sleep disorders
  • medication
  • alcool or toxic consumption
  • up to 300 mg caffeine per day consumption
  • neurologic, cardiovascular, metabolic, pulmonary psychiatric disease or disorder

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Sleep extension
Subject spend 10 hours Time in bed per day during 6 nights. This period is follow by a total sleep deprivation intervention (i.e. 39 hours awaking) in laboratory.
Subject are submitted to 39 hours of continuous awaking in laboratory and a recovery night
Other Names:
  • TSD
SHAM_COMPARATOR: Habitual sleep
Subject respect their habitual Time in bed during 6 nights. This period is follow by a total sleep deprivation intervention (i.e. 39 hours awaking) in laboratory.
Subject are submitted to 39 hours of continuous awaking in laboratory and a recovery night
Other Names:
  • TSD

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of errors during PVT (n)
Time Frame: Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery
number of errors (<100ms or > 500ms) during a10 min Psychomotor Vigilance test (PVT)
Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
median speed during PVT (s-1)
Time Frame: Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery
median speed response during a10 min Psychomotor Vigilance test (PVT)
Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery
number of micro sleep (n)
Time Frame: Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery
number of micro sleep (> 5 sec) per hour during baseline, TSD and recovery
Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery
Sleep latency (min)
Time Frame: Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery
Sleep latency during multiple sleep latency test (MSLT)
Every 3 hours, up to 24 hours of baseline, total sleep deprivation (TSD), and recovery
Muscular force (dyn)
Time Frame: At 10:00 on D1 (Baseline), D2 (TSD) and D3 (Recovery)
Muscular force developed by the subject
At 10:00 on D1 (Baseline), D2 (TSD) and D3 (Recovery)
Response to Trans Magnetic Stimulation (%)
Time Frame: At 10:00 on D1 (Baseline), D2 (TSD) and D3 (Recovery)
Effect of trans magnetic stimulation on Muscular force developed by the subject
At 10:00 on D1 (Baseline), D2 (TSD) and D3 (Recovery)
Polysomnographic classification (N1, N2, N3, REM)
Time Frame: night during DA (Baseline) and D3 (Recovery)
Evaluation of the duration of each sleep stages during the night before and after TSD
night during DA (Baseline) and D3 (Recovery)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Damien LEGER, MD, PhD, Sleep center, Hotel Dieu Paris
  • Study Director: Mounir CHENNAOUI, PhD, Institut de Recherche Biomédicale des Armées

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (ACTUAL)

September 1, 2014

Study Completion (ACTUAL)

December 1, 2014

Study Registration Dates

First Submitted

January 19, 2015

First Submitted That Met QC Criteria

January 27, 2015

First Posted (ESTIMATE)

February 2, 2015

Study Record Updates

Last Update Posted (ESTIMATE)

February 2, 2015

Last Update Submitted That Met QC Criteria

January 27, 2015

Last Verified

January 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • 14ca703op1
  • 2013-A01403-42 (OTHER: ANSM ID RCB)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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