Mindfulness training for high blood pressure in Black women
Telephone-based Mindfulness Training to Reduce Blood Pressure in Black Women With Hypertension in the Jackson Heart Study
This study is testing if a mindfulness training program can lower high blood pressure more effectively than a support group for Black women over six months.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 300 (estimated) |
| Ages | 18 Years to 99 Years |
| Sex | Female |
| Sponsor | NYU Langone Health Academic / other |
| Locations | 1 site (Jackson, Mississippi) |
| Trial ID | NCT06511479 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of two different programs aimed at reducing high blood pressure in Black women: a mindfulness training program called MIND-BP and a support group called BOOST. Both programs are conducted via Zoom and focus on helping participants manage stress and improve emotional regulation. The primary goal is to determine if the MIND-BP program results in greater reductions in systolic blood pressure compared to the BOOST program over a six-month period. Participants will be women involved in the Jackson Heart Study who meet specific eligibility criteria.
Who should consider this trial
Good fit: Ideal candidates for this study are Black women with high blood pressure who are participants in the Jackson Heart Study.
Not a fit: Patients who are currently pregnant, have severe depressive symptoms, or are participating in another trial may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a new, effective approach to managing hypertension in Black women through mindfulness techniques.
How similar studies have performed: Previous studies have shown that mindfulness programs can effectively lower blood pressure, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female participant in Jackson Heart Study * Willing to be randomized and comply with all aspects of protocol * Willing to be audio-recorded during group sessions. Exclusion Criteria: * Positive cognitive screen (MMSE \<19) * Severe depressive symptoms (CES-D ≥16) * Pregnant or planning to become pregnant in the next 6 months * Current participation in another trial * Arm circumference \>45 cm and \<22 cm
Where this trial is running
Jackson, Mississippi
- University of Mississippi Medical Center — Jackson, Mississippi, United States (Recruiting)
Study contacts
- Principal investigator: Tanya Spruill, PhD — NYU Langone Health
- Study coordinator: Tanya Spruill, PhD
- Email: Tanya.spruill@nyulangone.org
- Phone: 646-923-0626
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.