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Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care

Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care: A Pragmatic Randomized Controlled Trial

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* Age 18 years or older.
* Diagnosed hypertension documented prior to the index clinic visit.
* Scheduled for and attends an in-person visit with a participating clinician at a study clinic.
* Elevated BP (blood pressure) documented in Epic during rooming or the clinic visit before study enrollment, defined as systolic BP \>=140 mmHg or diastolic BP \>=90 mmHg.

Exclusion Criteria:

* Visit is canceled, rescheduled, or the patient does not attend the visit.
* Patient already has a usable home BP cuff provide through insurance within the past 5 years.
* Patient declines assistance obtaining a BP cuff.
* Patient declines submitting cuff order to insurance.
* Patient unable to participate for operational reasons.

About the study

The goal of this study is to identify what cuff delivery and BP log return modality most effectively achieve successful delivery of a self-measured blood pressure (SMBP) intervention in routine care, among adult primary care patients with uncontrolled hypertension?

What is being tested

• In-Clinic Cuff Delivery - Enhanced Return Conversation (behavioral)
• In-Clinic Cuff Delivery - Written Instructions (behavioral)
• Mail Order Cuff Delivery - Enhanced Return Conversation (behavioral)
• Mail Order Cuff Delivery - Written Instructions (behavioral)

Sponsor: Wake Forest University Health Sciences · Participants: 150 · Started: Jul 30, 2026

Contact the study team

• Rasha Khatib, PhD · Phone: 7086843691

Official record on ClinicalTrials.gov — NCT07693699

Locations in the U.S.

Conditions

• High Blood Pressure

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.