Clinical trial Recruiting at 6 sites Interventional Ages 18 and up

Optimizing how patients get blood pressure cuffs and how they log readings in primary care

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

Run by Wake Forest University Health Sciences · NCT07693699 · Data updated 2026-11-12

We’re testing the best way to provide a standard, validated blood pressure cuff and the easiest way for patients to log their readings in routine primary care among adults with uncontrolled hypertension.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment150 (estimated)
SponsorWake Forest University Health Sciences
Academic / other
Locations6 sites (Chicago, Illinois and 5 other locations)
StatusRecruiting
StartedJuly 30, 2026
Main results expectedOctober 20, 2026
Study endsNovember 20, 2026
Registry record updatedAugust 12, 2026
Trial IDNCT07693699 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults with diagnosed hypertension who have an upcoming in-person visit at a participating clinic and lack a usable home cuff obtained through insurance in the past five years.

Probably not a fit

Patients who already have a usable home cuff or those who do not attend the in-person visit may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study tests four delivery and instruction approaches to support self-measured blood pressure in primary care. Participants are adults with diagnosed hypertension who have elevated readings and are attending in-person visits at participating clinics. The trial compares mail-order versus in-clinic cuff delivery, each with either enhanced return conversation or written instructions for cuff use and BP logging. The aim is to identify scalable methods for cuff access and training that can be integrated into routine care without relying on research funds for devices.

Why it matters

Potential benefit: If successful, the study could provide scalable, sustainable ways for health systems to equip patients with cuffs and improve SMBP adoption.

How similar studies have gone: Previous pilots show SMBP uptake can improve in underserved settings, but this study tests scalable, real-world delivery methods.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Advocate Medical Group Chicago (Southeast)
    Chicago, Illinois, United States
    Recruiting
  • Advocate Medical Group Chicago (Imani Village)
    Chicago, Illinois, United States
    Recruiting
  • Advocate Medical Group Beverly
    Chicago, Illinois, United States
    Recruiting
  • Advocate Medical Group Merrionette Park
    Merrionette Park, Illinois, United States
    Recruiting
  • Advocate Medical Group Oak Lawn (FP)
    Oak Lawn, Illinois, United States
    Recruiting
  • Advocate Medical Group Oak Lawn (IM)
    Oak Lawn, Illinois, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.