NightWare Therapeutic Platform for improving Cardiovascular Health in Adults With Nightmares Associated with PTSD

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Description

We are recruiting individuals who experience PTSD-associated nightmares to participate in a research study to help us understand if improving sleep quality, by reducing the impact of nightmares can improve cardiovascular health.

Main Procedures Involved: Sleep monitoring and nightmare intervention, assessment of bone mineral density and body composition, ultrasound of blood vessels, cognitive and psychological assessments, blood draw

Duration of Participation: The whole study will span approximately 12-15 weeks.

Details
Age

Adult

Eligibility

1) Experience repetitive nightmares 2) Men and women age 22 years or older 3) No uncontrolled high blood pressure 4) Non-smoking 5) No history of cancer, diabetes, or cardiovascular/heart disease 6) No use of hormone therapy currently or in the last 6 months

Type of Study

Outcomes Research

Principal Investigator
Photograph of Kerrie Moreau,  PhD

Kerrie Moreau, PhD

Study ID

Protocol Number: 21-5027

More information available at ClinicalTrials.gov: NCT05365607

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