RECRUITING

Blood Pressure Lowering Strategies to Eliminate Hypertension Disparities (BLESSED)

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

The burden of hypertension and related cardiovascular diseases, stroke, and end-stage kidney disease is disproportionately high in Black populations, especially in the South. The Blood Pressure Lowering Strategies to Eliminate Hypertension Disparities (BLESSED) cluster randomized trial aims to test the effectiveness, implementation, and sustainability of a community health worker (CHW)-led multifaceted intervention compared to enhanced usual care for hypertension control in Black communities. In the BLESSED trial, the investigators plan to recruit 1,176 adults with hypertension (approximately 28 per church) from 42 predominantly Black churches in the Greater New Orleans area. The multifaceted intervention will last for 18 months, followed by a post-intervention follow-up visit at 24 months. The BLESSED trial aims to generate evidence regarding the effectiveness, implementation, and sustainability of this CHW-led church-based multifaceted intervention in eliminating hypertension disparities in the United States (US) general population.

Official Title

Blood Pressure Lowering Strategies to Eliminate Hypertension Disparities

Quick Facts

Study Start:2023-11-01
Study Completion:2027-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06133322

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Men or women aged ≥18 years
  2. 2. Community members associated with the participating churches (church members and their families and friends)
  3. 3. Systolic blood pressure ≥130 mmHg or diastolic blood pressure ≥80 mm Hg
  4. 4. Willing and able to participate in the intervention.
  5. 5. Willing and able to sign written informed consent.
  1. 1. Prior hospitalization in the last 3 months for chronic heart failure or heart attack
  2. 2. Current diagnosis of cancer requiring chemotherapy or radiation therapy
  3. 3. Stage-5 chronic kidney disease requiring chronic dialysis or transplant
  4. 4. Pregnant or planning to become pregnant in the next 18 months
  5. 5. Planning to move out of the Greater New Orleans area during the next year

Contacts and Locations

Study Locations (Sites)

Tulane University
New Orleans, Louisiana, 70112
United States

Collaborators and Investigators

Sponsor: Tulane University

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 Date2023-11-01
Study Completion Date2027-06-30

Study Record Updates

Study Start Date2023-11-01
Study Completion Date2027-06-30

Terms related to this study

Keywords Provided by Researchers

  • church-based
  • Black
  • African American
  • Community-based Intervention
  • health disparities
  • cardiovascular disease prevention

Additional Relevant MeSH Terms

  • Hypertension