RECRUITING

Acoustic Stimulation During Restricted Sleep After Sleep Deprivation

Conditions

Sleep Deprivation Sleep Restriction Acoustic Stimulation Performance Alertness

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Slow-wave Sleep Enhancement Using Acoustic Stimulation to Facilitate Performance Recovery During Restricted Sleep After Sleep Deprivation

Quick Facts

Study Start:2022-03-14

Study Completion:2026-10

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05309473

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.

Ages Eligible for Study:18 Years to 39 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT

Inclusion Criteria	Exclusion Criteria
* 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.	* 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

Inclusion Criteria

Exclusion Criteria

* 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.

* 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

Contacts and Locations

Study Contact

John D Hughes, MD

CONTACT

301-319-3214

john.d.hughes4.ctr@mail.mil

Study Locations (Sites)

Walter Reed Army Institute of Research

Silver Spring, Maryland, 20910

United States

Collaborators and Investigators

Sponsor: Walter Reed Army Institute of Research (WRAIR)

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 Registration Dates

Study Start Date2022-03-14

Study Completion Date2026-10

Study Record Updates

Study Start Date2022-03-14

Study Completion Date2026-10

Terms related to this study

Additional Relevant MeSH Terms

Sleep Deprivation
Sleep Restriction
Acoustic Stimulation
Performance
Alertness