The PCORnet Blood Pressure Home Monitoring Study

NACompletedINTERVENTIONAL
Enrollment

2,238

Participants

Timeline

Start Date

August 15, 2019

Primary Completion Date

October 23, 2021

Study Completion Date

October 23, 2021

Conditions
Hypertension
Interventions
DEVICE

Smartphone-linked HBPM and associated app

Participants in the Smartphone-linked arm of the study will receive an Omron 786N Home Blood Pressure Monitor (HBPM) that can be linked to the Omron Connect app via Bluetooth. They will also receive instructions about how to use their device and download the app and will be provided with publicly available guidelines for HBPM. Participants will be instructed to use their device and app to take readings which they can track over time and share with their provider using the app.

DEVICE

Standard HBPM

Participants in the Standard arm of the study will receive an Omron 785N Home Blood Pressure Monitor (HBPM), instructions about how to use their device and publicly available guidelines for HBPM. They will be instructed to use their device to take readings which they can track over time and share with their provider.

Trial Locations (4)

32610

University of Florida Health, Gainesville

55902

Mayo Clinic, Rochester

70112

University Medical Center, New Orleans

94143

University of California, San Francisco, San Francisco

All Listed Sponsors
collaborator

Patient-Centered Outcomes Research Institute

OTHER

lead

University of California, San Francisco

OTHER

NCT03796689 - The PCORnet Blood Pressure Home Monitoring Study | Biotech Hunter | Biotech Hunter