Examining the heart health of adults with trauma
The Effects of a Cognitive Behavioral Healthy Lifestyle Intervention for Cardiovascular Risk Reduction in Posttraumatic Stress Disorder
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.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 216 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Nova Southeastern University Academic / other |
| Locations | 1 site (Fort Lauderdale, Florida) |
| Trial ID | NCT05700201 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who exhibit PTSD symptoms and have identified cardiovascular risks.
Not a fit: Patients who are unable to engage in low to moderate physical activity, such as walking, will not benefit from this study.
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 performed: 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.
Eligibility criteria
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 this trial is running
Fort Lauderdale, Florida
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.