NightWare and Cardiovascular Health in Veterans With PTSD
NCT06419959
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
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.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Post-traumatic Stress Disorder (PTSD)
- Cardiovascular Diseases
- Autonomic Dysfunction
- Vascular Stiffness
- Nightmare
- Endothelial Dysfunction
- Veteran
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 22 to 88 years
- Sex
- All
- Healthy volunteers
- Accepted
- Sponsor
- VA Office of Research and Development
- Last updated on ClinicalTrials.gov
- October 8, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Colorado · 1
- Rocky Mountain Regional VA Medical Center, Aurora, CO · Aurora, CO
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.