Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Examining the heart health of adults with trauma

Official title: The Effects of a Cognitive Behavioral Healthy Lifestyle Intervention for Cardiovascular Risk Reduction in Posttraumatic Stress Disorder

Run by Nova Southeastern University · NCT05700201 · Data updated 2026-11-12

This study tests if a healthy lifestyle program can improve heart health in adults with PTSD by helping them overcome challenges like stress and sleep problems.

More Posttraumatic Stress Disorder trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment216 (estimated)
SponsorNova Southeastern University
Academic / other
Locations1 site (Fort Lauderdale, Florida)
StatusRecruiting
StartedApril 21, 2023
Main results expectedAugust 31, 2026
Study endsAugust 31, 2026
Registry record updatedAugust 6, 2026
Trial IDNCT05700201 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older who exhibit PTSD symptoms and have identified cardiovascular risks.

Probably not a fit

Patients who are unable to engage in low to moderate physical activity, such as walking, will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project investigates the effects of a healthy lifestyle intervention on cardiovascular health in adults suffering from posttraumatic stress disorder (PTSD). The study aims to address the elevated cardiovascular disease (CVD) risks associated with PTSD by implementing a tailored intervention that promotes healthy behaviors. Participants will be assessed over a one-year period to evaluate changes in health behaviors, cardiovascular risks, and CVD markers. The intervention specifically targets barriers to healthy living that are unique to individuals with PTSD, such as sleep disruptions and stress responses.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce cardiovascular risks in patients with PTSD, improving their overall health outcomes.

How similar studies have gone: While there is considerable evidence linking PTSD to cardiovascular risks, this specific approach to risk reduction through lifestyle intervention is relatively novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* PTSD symptoms
* overweight OR less than 30 min. of moderate physical activity 5 times per week

Exclusion Criteria:

* cannot exercise at a low-moderate level (walking)

Where it's running

  • College of Psychology, Nova Southeastern University
    Fort Lauderdale, Florida, United States
    Recruiting

Study contacts

  • Principal investigator: Jeffrey Kibler, PhD — Nova Southeastern University
  • Study coordinator: Shay Murphy
  • Email: whs.nsu@gmail.com
  • Phone: 954-262-5942

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.