RECRUITING

Jackson Heart Study Women's Hypertension Study

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

High blood pressure is a powerful risk factor for heart disease. Black women are more likely to have high blood pressure than white women or Hispanic women. Even when they are aware they have high blood pressure, many people struggle to keep their blood pressure controlled. Research shows a connection between life stress and high blood pressure and heart disease outcomes. Mindfulness training programs can help people regulate their emotions and cope with stress. Research shows that mindfulness programs can also lower blood pressure. This study will compare two programs: MIND-BP, a Zoom-based mindfulness training group; and BOOST, a Zoom-based support group. The aims of the study are to test if the MIND-BP program leads to greater reductions in blood pressure, stress and depressive symptoms than the BOOST program in Black women with high blood pressure who are participating in the Jackson Heart Study. The primary outcome measure is 6-month change in systolic blood pressure. The secondary outcome measures are 6-month changes in perceived stress and depressive symptoms.

Official Title

Telephone-based Mindfulness Training to Reduce Blood Pressure in Black Women With Hypertension in the Jackson Heart Study

Quick Facts

Study Start:2024-11-18
Study Completion:2027-05-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06511479

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Female participant in Jackson Heart Study
  2. * Willing to be randomized and comply with all aspects of protocol
  3. * Willing to be audio-recorded during group sessions.
  1. * Positive cognitive screen (MMSE \<19)
  2. * Severe depressive symptoms (CES-D ≥16)
  3. * Pregnant or planning to become pregnant in the next 6 months
  4. * Current participation in another trial
  5. * Arm circumference \>45 cm and \<22 cm

Contacts and Locations

Study Contact

Tanya Spruill, PhD
CONTACT
646-923-0626
Tanya.spruill@nyulangone.org

Principal Investigator

Tanya Spruill, PhD
PRINCIPAL_INVESTIGATOR
NYU Langone Health

Study Locations (Sites)

University of Mississippi Medical Center
Jackson, Mississippi, 39216
United States

Collaborators and Investigators

Sponsor: NYU Langone Health

  • Tanya Spruill, PhD, PRINCIPAL_INVESTIGATOR, NYU Langone Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11-18
Study Completion Date2027-05-30

Study Record Updates

Study Start Date2024-11-18
Study Completion Date2027-05-30

Terms related to this study

Additional Relevant MeSH Terms

  • Hypertension