Acoustic Stimulation During Restricted Sleep After Sleep Deprivation
Slow-wave Sleep Enhancement Using Acoustic Stimulation to Facilitate Performance Recovery During Restricted Sleep After Sleep Deprivation
Walter Reed Army Institute of Research (WRAIR)
44 participants
Mar 14, 2022
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to determine if brief sounds or tones presented within a restricted period of recovery sleep after a period of sleep deprivation will enhance restorative properties and improve performance during a subsequent period of wakefulness.
Eligibility
Inclusion Criteria2
- Healthy men and non-pregnant, non-lactating women 18 to 39 years of age (inclusive)
- Must demonstrate adequate comprehension of the protocol, by achieving a score of at least 80% correct on a short multiple-choice quiz. Individuals who fail to achieve a passing score on the initial quiz will be given one opportunity to retest after a review of protocol information. Individuals who fail the comprehension assessment for the second time will be disqualified.
Exclusion Criteria11
- You must have learned English as your first language
- You must have a body mass index (BMI) below 30 (this is a mathematical calculation of your height and weight)
- You must not have current or a history of sleeping problems (for example, insomnia or sleep apnea), or symptoms that indicate a potential sleep disorder
- You must get an average of 6-9 hours of sleep per night and maintain a normal sleep/wake schedule
- You must not drink excessive amounts of caffeine, alcohol, or smoke cigarettes regularly
- You must not be on certain medications (determined on a case by case basis)
- You must test negative for illicit drugs
- Women must not be pregnant or nursing
- You must not be participating in another ongoing clinical trial
- You must have a social security number or tax identification number in order to be paid for screening and participation in the study
- You cannot have a history of the following conditions: Cardiovascular disease, a neurologic disorder, pulmonary disease requiring inhaler use, kidney disease or kidney abnormalities, liver disease of liver abnormalities, a history of psychiatric disorder requiring hospitalization or medication within the last two years or for a continuous period of more than 6 months in the last ten years
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Interventions
Prior to bedtime on the first two recovery nights, a Philips SmartSleep device will be applied to the head of each subject. Subjects will receive acoustic stimulation during the four hours of sleep.
Prior to bedtime on the first two recovery nights, a Philips SmartSleep device will be applied to the head of each subject. Subjects will receive Sham (no acoustic stimulation) during the four hours of sleep.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05309473