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 type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | Wake Forest University Health Sciences Academic / other |
| Locations | 6 sites (Chicago, Illinois and 5 other locations) |
| Status | Recruiting |
| Started | July 30, 2026 |
| Main results expected | October 20, 2026 |
| Study ends | November 20, 2026 |
| Registry record updated | August 12, 2026 |
| Trial ID | NCT07693699 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
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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
- Principal investigator: Rasha Khatib, PhD — Advocate Health
- Study coordinator: Rasha Khatib, PhD
- Email: Rasha.Alkhatib@aah.org
- Phone: 7086843691
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.