Clin2
NCT07021014Possibly a fitNot yet recruiting

NightWare device for heart health in women with PTSD

Post Traumatic Stress DisorderCardiovascular DiseasesAutonomic DysfunctionVascular StiffnessNightmareEndothelial DysfunctionKidney DiseasesRenal Dysfunction

Part of Brain & nervous system, Heart & circulation, Kidney & urinary, Mental health, Women’s health & pregnancy clinical trials.

This study tests a watch-like device called NightWare that helps reduce nightmares in women with PTSD to see if it also improves heart health. Participants will use the device at night, and researchers will check blood vessel function and other heart-related measures.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
36 people
Ages
22 years to 40 years
Study type
Interventional

Who can take part

  • You are a woman (studies are for women with and without PTSD).
  • If you have PTSD, you must have experienced trauma, have nightmares that bother you, and have poor sleep quality.
  • You are generally healthy — no unstable medical conditions like uncontrolled high blood pressure, active heart disease, or cancer.
  • You are not taking certain medications (like blood pressure, cholesterol, or weight-loss drugs) and are willing to stop vitamins or supplements 2 weeks before the study.
  • You are not pregnant, breastfeeding, or less than 12 months after giving birth.
  • You have access to wireless internet and two power outlets near your bed (needed for the device).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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