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Transcranial Electrical Stimulation (TES) at Slow Oscillation (SO) Frequency During NREM Sleep

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date: Jun 2023 to Jun 2027
    • Study completion date: Jul 2023 to Dec 2027
    v10
  2. Primary completion date: Jun 2021 to Jun 2023
    • Study completion date: Jul 2022 to Jul 2023
    v9
  3. Primary completion date: Jun 2020 to Jun 2021
    • Study completion date: Jul 2021 to Jul 2022
    v8
  4. Primary completion date: Jun 2019 to Jun 2020
    • Study completion date: Jul 2019 to Jul 2021
    v7
  5. Primary completion date: Jun 2018 to Jun 2019
    • Site contact updated
    v6
Show 4 earlier versionsHide 4 earlier versions
  1. Primary completion date: Jun 2017 to Jun 2018
    • Study completion date: Jul 2017 to Jul 2019
    v5
  2. Eligibility criteria shortened, about 16 wordsv4
  3. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date: May 2017 to Oct 27, 2016
    v3
  4. Secondary endpoints: details revised at 1 of 6 entriesv2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to determine if the enhancement of electroencephalographic (EEG) slow-wave activity using transcranial electrical stimulation (TES) at Slow Oscillation (SO) frequency, during a restricted period of nocturnal sleep, enhances the restorative properties of that period of sleep and improves performance during a subsequent period of sleep deprivation.
Trial Details
NCT Number NCT02945501
Lead Sponsor U.S. Army Medical Research and Development Command
Collaborators: Walter Reed Army Institute of Research (WRAIR)
Conditions
(from sponsor)		 Sleep Deprivation, Mental Competency
Related terms Sleep Deprivation
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov