A program to improve cardiovascular health in Black men
Black Impact: The Mechanisms Underlying Psychosocial Stress Reduction in a Cardiovascular Health Intervention
NA · Ohio State University · NCT06055036
This study tests a 24-week program designed to help Black men improve their heart health through exercise, education, and support from health coaches.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 340 (estimated) |
| Ages | 18 Years and up |
| Sex | Male |
| Sponsor | Ohio State University (other) |
| Locations | 1 site (Columbus, Ohio) |
| Trial ID | NCT06055036 on ClinicalTrials.gov |
What this trial studies
This intervention focuses on enhancing cardiovascular health among Black men by addressing psychosocial stress and promoting lifestyle changes. The Black Impact program is a 24-week initiative that includes weekly physical activity sessions, health education, and support from health coaches and community health workers. The program targets individuals with less-than-ideal cardiovascular health metrics, aiming to improve their overall health outcomes through community engagement and structured activities.
Who should consider this trial
Good fit: Ideal candidates for this program are Black men aged 18 and older with suboptimal cardiovascular health scores.
Not a fit: Patients who have healthcare provider-imposed limitations on physical activity may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could significantly improve cardiovascular health and life expectancy for Black men.
How similar studies have performed: While there is limited literature on similar interventions specifically for Black men, preliminary pilot testing has shown promising feasibility and acceptability.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * The inclusion criteria are: 1) Black men (self-report); 2) adult age 18 years or older; 3) Life's Essential 8 total average score \< 80; 4) English speaking; and 5) lives in Metropolitan Columbus, Ohio. Exclusion Criteria: * healthcare provider-imposed limitations on physical activity.
Where this trial is running
Columbus, Ohio
- The Ohio State University — Columbus, Ohio, United States (RECRUITING)
Study contacts
- Principal investigator: Joshua Joseph, MD — Ohio State University
- Study coordinator: Sean Matambo
- Email: Sean.Matambo@osumc.edu
- Phone: 773-683-9241
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.
Conditions: Cardiometabolic Syndrome, Physical Inactivity, Hypertension, Type 2 Diabetes, PreDiabetes, Obesity, Cardiovascular Diseases, Smoking