Implementing a Home Blood Pressure Monitoring Program in Primary Care
NCT ID: NCT05885997
Last Updated: 2025-04-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
23928 participants
INTERVENTIONAL
2023-11-01
2026-11-01
Brief Summary
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Detailed Description
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While there is strong evidence for Supported HBPM from pragmatic randomized controlled trials (RCTs), the evidence has been generated from the subgroup of patients and clinicians who volunteered to participate in trials, and the sample sizes have been in the hundreds of patients. There remains a gap in assessing the effectiveness of a scaled-up HBPM program that seeks to maximize the enrollment of primary care patients with uncontrolled hypertension.
Accordingly, in partnership with health system leaders at New York-Presbyterian Hospital (NYP), Columbia University Irving Medical Center, and Weill Cornell Medicine, the study investigator leveraged a system-wide investment in telemedicine to develop a telemonitoring-enabled Supported HBPM program. The Supported HBPM program consists of two options for obtaining electronic health record (EHR)-integrated home BP data. The low resource intensity option is designed for patients that can obtain valid home BP devices and are comfortable using the patient portal. It includes digital support to prompt patients to track their home BP readings in the patient portal using their own BP devices with automated triage support for extreme readings. The high resource intensity option is designed for patients that need additional support with HBPM. It involves navigator support with obtaining and using loaned home BP devices that wirelessly transmit data into the EHR and nursing support to triage extreme readings. Both programs can be ordered by clinicians in the EHR and both provide clinicians with weekly summaries of home BP readings with average home BP already calculated.
The study investigator concurrently followed a theory-driven process (the Behavior Change Wheel) to develop an implementation strategy aimed at increasing uptake of the Supported HBPM program. The study investigator now plans to implement and evaluate the Supported HBPM program across practices in the NYP, Weill Cornell Medicine, and ColumbiaDoctors primary care network which is comprised of a socioeconomically diverse patient population.
The study will evaluate the program by conducting a parallel-group cluster randomized trial in which 15 practices will be matched and then randomly assigned to early implementation of the Supported HBPM program (intervention) versus usual care with delayed implementation (i.e., wait-list control). Data will be retrospectively collected from a 12 month period before implementation (pre-implementation periods) as well as from a 12 month period after implementation (post-implementation period) to assess outcomes.
If successful, this project will provide a roadmap for widely implementing an EHR-integrated Supported HBPM program, and will accelerate a change in the paradigm of hypertension management from the office to the home.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Intervention Clinics, Pre-Implementation Period
Usual care
Usual care
Usual care
Intervention Clinics, Post-Implementation Period
Access to Supported HBPM program plus a multifaceted implementation strategy designed to increase uptake of the program by primary care patients with uncontrolled hypertension
Supported HBPM program plus multifaceted implementation strategy
Supported HBPM Program:
* Patients are loaned a wireless home BP device or use their own device
* Navigator or app support for onboarding and engaging patients in HBPM
* Nursing or app support for monitoring and triaging home BP data for extreme readings
* EHR integration of order for program and home BP data, with weekly feedback of home BP results to clinicians within the EHR
Multifaceted implementation strategy:
* Clinician education about the benefits of the program as well as training in how to refer and manage patients who are enrolled
* Prompts and reminders to increase clinician referrals
* Instructional materials for patients and clinicians
* Problem-solving meetings to tailor implementation for individual practices
Control Clinics, Pre-Implementation Period
Usual care
Usual care
Usual care
Control Clinics, Post-Implementation Period
Usual care
Usual care
Usual care
Interventions
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Usual care
Usual care
Supported HBPM program plus multifaceted implementation strategy
Supported HBPM Program:
* Patients are loaned a wireless home BP device or use their own device
* Navigator or app support for onboarding and engaging patients in HBPM
* Nursing or app support for monitoring and triaging home BP data for extreme readings
* EHR integration of order for program and home BP data, with weekly feedback of home BP results to clinicians within the EHR
Multifaceted implementation strategy:
* Clinician education about the benefits of the program as well as training in how to refer and manage patients who are enrolled
* Prompts and reminders to increase clinician referrals
* Instructional materials for patients and clinicians
* Problem-solving meetings to tailor implementation for individual practices
Eligibility Criteria
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Inclusion Criteria
* At least one completed primary care office visit during relevant 6-month pre implementation or post-implementation study time period
* Age 18-85 years old
* Primary care practice that provides care to adult patients affiliated with New York Presbyterian's Ambulatory Care Network, ColumbiaDoctors, or Weill Cornell Medicine, including practices that specialize in HIV medicine
Exclusion Criteria
* Pregnancy during measurement period (as per ICD-10 codes)
* Stage 5 or end-stage kidney disease (as per ICD-10 codes)
* Terminal illness/in hospice care (as per ICD-10 codes)
Practice-level
* Medical director declines participation in the trial
* Site for pilot testing the supported HBPM program or its implementation strategy
18 Years
85 Years
ALL
No
Sponsors
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Weill Medical College of Cornell University
OTHER
New York Presbyterian Hospital
OTHER
National Heart, Lung, and Blood Institute (NHLBI)
NIH
Columbia University
OTHER
Responsible Party
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Ian Kronish
Associate Professor of Medicine at CUIMC, Associate Director of the Center for Behavioral Cardiovascular Health
Principal Investigators
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Ian Kronish, MD
Role: PRINCIPAL_INVESTIGATOR
Columbia University
Locations
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Columbia University Irving Medical Center
New York, New York, United States
Weill Medical College of Cornell University
New York, New York, United States
Countries
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Other Identifiers
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AAAS5544
Identifier Type: -
Identifier Source: org_study_id
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