Actively Recruiting

Phase Not Applicable
Age: 21Years - 85Years
All Genders
ID06527794

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

Age: 21Years - 85Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

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

Long-term Monitoring

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

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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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