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NCT05309473 · ClinicalTrials.gov registry record · NA
Acoustic Stimulation During Restricted Sleep After Sleep Deprivation
A NA study of Sleep Deprivation and Sleep Restriction, sponsored by Walter Reed Army Institute of Research (WRAIR).
- Recruiting
- Registry status
- NA
- Development phase
- 44
- Enrollment target
- 1
- Study location
NCT05309473: Recruiting NA study of Sleep Deprivation and Sleep Restriction, sponsored by Walter Reed Army Institute of Research (WRAIR).
NCT05309473 is a NA study of Sleep Deprivation and Sleep Restriction that is actively recruiting participants, run by Walter Reed Army Institute of Research (WRAIR). The registered enrollment target is 44 participants, below the 90-participant average among 34 other Sleep Deprivation trials with a reported enrollment target (51% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05309473, a NA study of Sleep Deprivation and Sleep Restriction, is actively recruiting participants, sponsored by Walter Reed Army Institute of Research (WRAIR).
- RECRUITING
- Registry status
- NA
- Development phase
- 44 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
Performed at approximately 75 minutes intervals throughout the sleep deprivation and recovery days
Conditions Studied
Interventions
- DEVICE Philips SmartSleep Acoustic Stimulation Device
- DEVICE Sham (no Acoustic Stimulation)
Study Locations (1)
Maryland
- Walter Reed Army Institute of Research - Silver Spring
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2022-03-14 |
| Est. Completion | 2026-10 |
| Phase | NA |
What NCT05309473 shows while recruiting
NCT05309473 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 90-participant average among 34 other Sleep Deprivation trials with a reported enrollment target (51% lower).
The record links to 5 conditions, with Sleep Deprivation appearing as the primary indexed condition, and to 2 interventions - of which Philips SmartSleep Acoustic Stimulation Device is the first listed.
NCT05309473 reports a single indexed study location in Maryland.
Frequently Asked Questions
What is clinical trial NCT05309473 about?
NCT05309473 is a clinical study titled "Acoustic Stimulation During Restricted Sleep After Sleep Deprivation". 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.
What is the current status of trial NCT05309473?
This trial is currently recruiting. It is a NA study. The enrollment target is 44 participants. The study started on 2022-03-14. Estimated completion is 2026-10.
What conditions does trial NCT05309473 study?
This clinical trial studies the following conditions: Sleep Deprivation, Sleep Restriction, Acoustic Stimulation, Alertness, Performance.
What interventions are being tested in trial NCT05309473?
The interventions under investigation include: Philips SmartSleep Acoustic Stimulation Device (DEVICE), Sham (no Acoustic Stimulation) (DEVICE).
Who is sponsoring clinical trial NCT05309473?
This trial is sponsored by Walter Reed Army Institute of Research (WRAIR), which has 12 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05309473 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Sleep Deprivation
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05309473's enrollment target sits among peer trials
44 24th of 34 higher than 10 of 34 other Sleep Deprivation trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Sleep Deprivation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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