Who is eligible for clinical trial NCT07693699?

Participants must meet protocol criteria for Hypertension. Confirm exact inclusion and exclusion requirements with the study coordinator.

Does clinical trial NCT07693699 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2026-08-10

Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care (NCT07693699)

🟢 Recruiting Observational / Diagnostic 🧠 Behavioral & Psychological Program Sponsor: Wake Forest University Health Sciences

🩺 Plain-English Summary (8th-Grade Level)

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?

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (4 items) and avoid the listed exclusions (6 items).

Location: Advocate Medical Group Chicago (Southeast) — Chicago, Illinois

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

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.

Usually NOT eligible if any of the following apply:

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.

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (6 Sites)

Advocate Medical Group Chicago (Southeast) — Chicago, Illinois
Advocate Medical Group Chicago (Imani Village) — Chicago, Illinois
Advocate Medical Group Beverly — Chicago, Illinois
Advocate Medical Group Merrionette Park — Merrionette Park, Illinois
Advocate Medical Group Oak Lawn (FP) — Oak Lawn, Illinois
Advocate Medical Group Oak Lawn (IM) — Oak Lawn, Illinois

💰 Cost, Insurance & Patient Rights

100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

🏛️ View Official NIH Record ↗