Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care
NCT07693699
This study is recruiting at 6 US sites in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
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?
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Hypertension
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Wake Forest University Health Sciences
- Last updated on ClinicalTrials.gov
- August 12, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Illinois · 6
- Advocate Medical Group Beverly · Chicago, IL
- Advocate Medical Group Chicago (Imani Village) · Chicago, IL
- Advocate Medical Group Chicago (Southeast) · Chicago, IL
- Advocate Medical Group Merrionette Park · Merrionette Park, IL
- Advocate Medical Group Oak Lawn (FP) · Oak Lawn, IL
- Advocate Medical Group Oak Lawn (IM) · Oak Lawn, IL
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.