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Acoustic Stimulation During Restricted Sleep After Sleep Deprivation

NCT05309473 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2024-04-23

No results posted yet for this 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.

Conditions

  • Sleep Deprivation
  • Sleep Restriction
  • Acoustic Stimulation
  • Performance
  • Alertness

Interventions

DEVICE

Philips SmartSleep Acoustic Stimulation Device

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.

DEVICE

Sham (no Acoustic Stimulation)

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.

Sponsors & Collaborators

  • Philips Healthcare

    collaborator INDUSTRY

  • Walter Reed Army Institute of Research (WRAIR)

    lead FED

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-14
Primary Completion
2025-10-31
Completion
2026-10-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT05309473 on ClinicalTrials.gov