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NightWare and Cardiovascular Health in Veterans With PTSD

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 12 months later Sep 30, 2026 → Sep 30, 2027
See other at-risk trials from VA Office of Research and Development

Record History

  1. Notable Primary completion pushed from Sep 30, 2026 to Sep 30, 2027 Completion pushed from Dec 31, 2026 to Dec 31, 2027 Show 1 more changeShow less
    • Completion pushed from Dec 31, 2026 to Dec 31, 2027
  2. Minor Eligibility criteria expanded, about 23 words Site contact updated Show 1 more changeShow less
    • Site contact updated
  3. Notable Trial status: Not Yet Recruiting to Recruiting Completion date: Sep 30, 2026 to Dec 31, 2026 · Start date changed from estimate of Sep 1, 2025 to Sep 10, 2025 · Site details revisedv8 Show 3 more changesShow less
    • Completion date: Sep 30, 2026 to Dec 31, 2026
    • Start date changed from estimate of Sep 1, 2025 to Sep 10, 2025
    • Site details revised
  4. Notable Start date: Jul 28, 2025 to Sep 1, 2025v7
  5. Notable Start date: Apr 21, 2025 to Jul 28, 2025v6
Show 4 earlier versionsHide 4 earlier versions
  1. Notable Start date: Feb 17, 2025 to Apr 21, 2025v5
  2. Notable Start date: Jan 1, 2025 to Feb 17, 2025v4
  3. Minor Re-verified, no change to tracked fieldsv3
  4. Notable Start date: Oct 1, 2024 to Jan 1, 2025 Site details revisedv2 Show 1 more changeShow less
    • Site details revised
  1. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
The purpose of this study is to learn more about the effectiveness of a prescription wrist-wearable device called NightWare (NW) on improving sleep in Veterans with nightmares related to posttraumatic stress disorder (PTSD). The investigators also want to learn whether it improves cardiovascular health among this population.
Trial Details
NCT Number NCT06419959
Lead Sponsor VA Office of Research and Development
Conditions Post-traumatic Stress Disorder (PTSD), Cardiovascular Diseases, Autonomic Dysfunction, Vascular Stiffness, Nightmare, Endothelial Dysfunction, Veteran
Enrollment 125 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov