Actively Recruiting
Remote Hypertension Tracking, Help, and Management to Reduce Disparities in Black Patients
Led by Wake Forest University Health Sciences · Updated on 2026-06-02
864
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
W
Wake Forest University Health Sciences
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating two different ways to manage hypertension in Black patients who have uncontrolled blood pressure. The study compares home blood pressure telemonitoring supported by a pharmacist and a community health worker with usual clinic-based care that includes a home blood pressure monitor and routine provider care. This pragmatic trial aims to reduce disparities in blood pressure control among Black patients. Participants will be randomly assigned to one of two groups. One group will receive remote blood pressure monitoring with medication management by a centralized team led by a pharmacist, plus social support, lifestyle education, and community resource connections provided by a community health worker. The other group will receive enhanced usual care, including training for providers on guideline-based therapy, a standardized education packet, and a home blood pressure monitor for regular measurements. During the study, patients will have their blood pressure and health outcomes monitored at baseline, 6 months, 12 months, 18 months, and 24 months. Various surveys will assess self-management skills, medication adherence, and patient care experiences. Researchers will measure the percentage of patients achieving blood pressure control, defined as a systolic blood pressure below 130 mmHg at 12 months, along with other health utilization data. The study will continue through September 2028.
CONDITIONS
Brief Title
Remote Hypertension Management for Black Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Self-identify as Black or African American
- Diagnosed with hypertension
- Aged 21 to 85 years
- Uncontrolled blood pressure defined by recent systolic blood pressure readings of 140 mmHg or higher as specified
- Receiving primary care at a participating clinic
- Able to speak English
You will not qualify if you...
- Currently pregnant or planning pregnancy during the study period
- Living in a long-term care facility, hospice, or having a terminal illness with less than 1 year life expectancy
- Estimated Glomerular Filtration Rate less than 30 ml/min or on dialysis (patients with functioning kidney transplant are eligible)
- Unable to provide informed consent or participate in study procedures
- Currently participating in another blood pressure management program
- Planning to move out of the area within the next 12 months
- Hispanic ethnicity
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 24 months
Participants receive either home blood pressure telemonitoring with remote medication management and social support, or enhanced usual care with education materials and a home blood pressure monitor.
Baseline visit and follow-up visits at Month 6, Month 12, and Month 18
Duration - Up to 24 months
Participants are monitored for health outcomes and healthcare utilization following treatment.
Follow-up visit at Month 24
Trial Site Locations
Total: 1 location
1
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States, 27157
Actively Recruiting
Research Team
Y
Yhenneko J. Taylor, PhD
A
Asha Ganesan
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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