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Interest of Cardiac Coherence in the Prevention of Chronic Post-traumatic Stress Disorder: Pilot Study

Study acronym: COHEPS-P
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Primary completion date: May 2024 to May 2027
    • Study completion date: Aug 2024 to May 2027
    v7
  2. Notable Primary completion date: Mar 2023 to May 2024
    • Study completion date: Jul 2023 to Aug 2024
    v6
  3. Notable Primary completion date: Sep 2021 to Mar 2023
    • Study completion date: Oct 2021 to Jul 2023
    v5
  4. Notable Trial status: Not Yet Recruiting to Recruitingv4 Show 4 more changesShow less
    • Primary completion date: Aug 2021 to Sep 2021
    • Study completion date: Aug 2021 to Oct 2021
    • Start date changed from estimate of Jun 2021 to Jul 19, 2021
    • Site details revised
  5. Notable Start date: Mar 2021 to Jun 2021
    • Secondary endpoints: 17 to 11
    v3
  6. Minor Secondary endpoints: details revised at 1 of 17 entriesv2
  7. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
ThThe aim of this study is to determinate the potential benefits of a respiratory training program (cardiac coherence, CC) in patients suffering from acute stress disorder, after a potentially traumatic event. Using this method is supposed to prevent the onset of chronic post traumatic stress disorder after 3 months. This pilot study will help to determinate the need of developing this kind of complementary and alternative program, and will also provide knowledge about the feasibiility and acceptability of this program for the patients.
Trial Details
NCT Number NCT04701723
Lead Sponsor Centre Hospitalier Universitaire de la Réunion
Conditions
(from sponsor)
Post-traumatic Stress Disorder
Related terms Stress Disorders, Post-Traumatic
Enrollment 44 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov