Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care
Public ClinicalTrials.gov record NCT07693699. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care: A Pragmatic Randomized Controlled Trial
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
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?
Study identification
- NCT ID
- NCT07693699
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 150 participants
Conditions and interventions
Conditions
Interventions
- 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
Behavioral
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jul 29, 2026
- Primary completion
- Oct 19, 2026
- Completion
- Nov 19, 2026
- Last update posted
- Aug 11, 2026
2026
United States locations
- U.S. sites
- 6
- U.S. states
- 1
- U.S. cities
- 3
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Advocate Medical Group Chicago (Southeast) | Chicago | Illinois | 60617 | Recruiting |
| Advocate Medical Group Chicago (Imani Village) | Chicago | Illinois | 60619 | Recruiting |
| Advocate Medical Group Beverly | Chicago | Illinois | 60643 | Recruiting |
| Advocate Medical Group Merrionette Park | Merrionette Park | Illinois | 60803 | Recruiting |
| Advocate Medical Group Oak Lawn (FP) | Oak Lawn | Illinois | 60453 | Recruiting |
| Advocate Medical Group Oak Lawn (IM) | Oak Lawn | Illinois | 60453 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT07693699, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 11, 2026 · Synced Sep 6, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT07693699 live on ClinicalTrials.gov.