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Implementing a Home Blood Pressure Monitoring Program in Primary Care (MonitorBP)

Primary Purpose

Hypertension

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Supported HBPM program plus multifaceted implementation strategy
Usual care
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Hypertension focused on measuring home blood pressure monitoring, remote patient monitoring, self-measured blood pressure monitoring, implementation science

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Patient-level Inclusion Criteria: Hypertension (as per International Statistical Classification of Diseases and Related Health Problems (ICD)-10 codes) 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 Exclusion Criteria: Advanced dementia or other measure of frailty (as per ICD-10 codes) 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) Do not reside in New York State Practice-level Inclusion Criteria: 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: Medical director declines participation in the trial Site for pilot testing the supported HBPM program or its implementation strategy

Sites / Locations

  • Columbia University Irving Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Other

Other

Arm Label

Intervention Clinics, Pre-Implementation Period

Intervention Clinics, Post-Implementation Period

Control Clinics, Pre-Implementation Period

Control Clinics, Post-Implementation Period

Arm Description

Usual care

Access to supported HBPM program plus a multifaceted implementation strategy designed to increase uptake of the program by primary care patients with uncontrolled hypertension

Usual care

Usual care

Outcomes

Primary Outcome Measures

Change in patient's office systolic blood pressure (SBP)
Change in patient's office systolic blood pressure (SBP) from index visit to last visit during the subsequent 12 months, among patients with uncontrolled hypertension at the index visit

Secondary Outcome Measures

Office diastolic blood pressure (DBP)
Change in patient's office diastolic blood pressure (DBP) from index visit to last visit during the subsequent 12 months, among patients with uncontrolled hypertension at the index visit
Change in patient's antihypertensive medication regimen intensity
Change in patient's antihypertensive medication regimen intensity as calculated by the Therapeutic Intensity Score from index visit to last visit during the subsequent 12 months, among patients with uncontrolled hypertension at the index visit
Antihypertensive medication adherence
Proportion of days covered by antihypertensive medications during the last 6 months of the 12-month follow-up period, among patients with uncontrolled hypertension at the index visit. Antihypertensive medication adherence will be calculated for each prescribed class of medication and then averaged across all classes.
Uncontrolled hypertension
Percentage of patients whose last office BP during the 12-month follow-up period was SBP>= 140 mmHg or DBP >= 90 mmHg, among all eligible patients

Full Information

First Posted
May 23, 2023
Last Updated
August 28, 2023
Sponsor
Columbia University
Collaborators
Weill Medical College of Cornell University, New York Presbyterian Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05885997
Brief Title
Implementing a Home Blood Pressure Monitoring Program in Primary Care
Acronym
MonitorBP
Official Title
Implementing a Home Blood Pressure Monitoring Program to Improve Hypertension Control in a Primary Care Network: the MonitorBP Cluster Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 1, 2023 (Anticipated)
Primary Completion Date
November 1, 2025 (Anticipated)
Study Completion Date
November 1, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
Weill Medical College of Cornell University, New York Presbyterian Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this research is to determine whether a theory-informed implementation strategy is successful at increasing the uptake of a supported home blood pressure monitoring (HBPM) program comprised of navigator support and wireless home BP monitoring as well as to determine the effectiveness of this evidence-based practice when implemented across multiple practices serving a diverse patient population.
Detailed Description
Hypertension guidelines now strongly recommend that patients with hypertension monitor their blood pressure (BP) at home (i.e., home BP monitoring; HBPM) as an approach to improving BP control so long as HBPM is conducted with clinical support (i.e., supported HBPM). Yet, few health systems have systematically implemented HBPM programs, and less than 20% of hypertensive patients routinely measure their BP at home, resulting in a gap in the translation of evidence-based recommendations into practice. 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 HBPM program with navigator and nursing support. 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 wireless, 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 a supported, wireless home BP device, electronic health record (EHR)-integrated HBPM program, and will accelerate a change in the paradigm of hypertension management from the office to the home.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
home blood pressure monitoring, remote patient monitoring, self-measured blood pressure monitoring, implementation science

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Data analysts will be blinded to group assignment when analyzing electronic health record data to determine the effectiveness of the program.
Allocation
Randomized
Enrollment
16000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention Clinics, Pre-Implementation Period
Arm Type
Experimental
Arm Description
Usual care
Arm Title
Intervention Clinics, Post-Implementation Period
Arm Type
Experimental
Arm Description
Access to supported HBPM program plus a multifaceted implementation strategy designed to increase uptake of the program by primary care patients with uncontrolled hypertension
Arm Title
Control Clinics, Pre-Implementation Period
Arm Type
Other
Arm Description
Usual care
Arm Title
Control Clinics, Post-Implementation Period
Arm Type
Other
Arm Description
Usual care
Intervention Type
Behavioral
Intervention Name(s)
Supported HBPM program plus multifaceted implementation strategy
Intervention Description
Supported HBPM Progam: Wireless home BP devices Navigator support for onboarding and engaging patients in HBPM Nursing support for monitoring home BP data for extreme readings Multifaceted implementation strategy: EHR integration of HBPM order and data 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 Problem-solving meetings to tailor implementation for individual practices
Intervention Type
Other
Intervention Name(s)
Usual care
Intervention Description
Usual care
Primary Outcome Measure Information:
Title
Change in patient's office systolic blood pressure (SBP)
Description
Change in patient's office systolic blood pressure (SBP) from index visit to last visit during the subsequent 12 months, among patients with uncontrolled hypertension at the index visit
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Office diastolic blood pressure (DBP)
Description
Change in patient's office diastolic blood pressure (DBP) from index visit to last visit during the subsequent 12 months, among patients with uncontrolled hypertension at the index visit
Time Frame
12 months
Title
Change in patient's antihypertensive medication regimen intensity
Description
Change in patient's antihypertensive medication regimen intensity as calculated by the Therapeutic Intensity Score from index visit to last visit during the subsequent 12 months, among patients with uncontrolled hypertension at the index visit
Time Frame
12 months
Title
Antihypertensive medication adherence
Description
Proportion of days covered by antihypertensive medications during the last 6 months of the 12-month follow-up period, among patients with uncontrolled hypertension at the index visit. Antihypertensive medication adherence will be calculated for each prescribed class of medication and then averaged across all classes.
Time Frame
12 months
Title
Uncontrolled hypertension
Description
Percentage of patients whose last office BP during the 12-month follow-up period was SBP>= 140 mmHg or DBP >= 90 mmHg, among all eligible patients
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Patient-level Inclusion Criteria: Hypertension (as per International Statistical Classification of Diseases and Related Health Problems (ICD)-10 codes) 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 Exclusion Criteria: Advanced dementia or other measure of frailty (as per ICD-10 codes) 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) Do not reside in New York State Practice-level Inclusion Criteria: 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: Medical director declines participation in the trial Site for pilot testing the supported HBPM program or its implementation strategy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maria-Jose Lopez-Sanchez, MPH
Phone
212-342-1335
Email
ml4419@cumc.columbia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ian Kronish, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Irving Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
A de-identified data archive that contains raw study data will be posted on an open science platform.
IPD Sharing Time Frame
After completion of major study activities.
IPD Sharing Access Criteria
Access to the data archive will be provided upon request

Learn more about this trial

Implementing a Home Blood Pressure Monitoring Program in Primary Care

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