Status:
COMPLETED
The PCORnet Blood Pressure Home Monitoring Study
Lead Sponsor:
University of California, San Francisco
Collaborating Sponsors:
Patient-Centered Outcomes Research Institute
Conditions:
Hypertension
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The PCORnet Blood Pressure Home Monitoring (BP HOME) Study is a patient-level randomized controlled trial that will compare the effectiveness of home blood pressure monitoring (HPBM) with versus witho...
Detailed Description
We have designed a patient-level randomized controlled trial that will compare the effectiveness of Smartphone-linked versus standard HBPM for helping patients with uncontrolled hypertension achieve a...
Eligibility Criteria
Inclusion
- Age ≥ 18 years
- At least one ambulatory visit in one of the participating study sites during the past year
- SBP \> 145 mmHg at most recent clinic visit (may be treated with BP meds already or not)
- A self-reported commitment to "work on lowering your blood pressure by 10 points or more to reduce your risk of heart attack and stroke"
- Owns a Smartphone (Android or iOS)
- Willing to receive text messages from the study
- Can read/write English well enough to use English-based Smartphone apps and fill out online surveys in English
Exclusion
- Has an arm circumference \<22 cm or \>42 cm
- Owns a functioning HPBM and has used it in the last 3 months
Key Trial Info
Start Date :
August 15 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 23 2021
Estimated Enrollment :
2238 Patients enrolled
Trial Details
Trial ID
NCT03796689
Start Date
August 15 2019
End Date
October 23 2021
Last Update
November 16 2022
Active Locations (4)
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1
University of California, San Francisco
San Francisco, California, United States, 94143
2
University of Florida Health
Gainesville, Florida, United States, 32610
3
University Medical Center
New Orleans, Louisiana, United States, 70112
4
Mayo Clinic
Rochester, Minnesota, United States, 55902