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Team-Based Home Blood Pressure Monitoring

Identifying Successful Strategies for Implementing Team-Based Home Blood Pressure Monitoring in Primary Care

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05488795
Acronym
TB-HBPM
Enrollment
5760
Registered
2022-08-05
Start date
2022-10-01
Completion date
2026-08-31
Last updated
2026-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Blood Pressure, Hypertension

Keywords

Home blood pressure monitoring, Hypertension control, Primary Care Teams, Implementation Research, Health Equity, Clinical Trial

Brief summary

The overall goal of this study is to identify and rigorously evaluate strategies for implementing and sustaining team-based home blood pressure monitoring (TB-HBPM) within primary care. The TB-HBPM intervention is a multifaceted program involving patient transmission of blood readings to EHR and clinical decision support. Implementation strategies include group-based education on hypertension measurement, target blood pressure goals, drug and lifestyle management, referral to community resources, and team training designed to optimize the coordination of hypertension care, and monthly audit and feedback reports to teams and clinicians. Hypertension control rates are suboptimal in many primary care practices with persistent racial disparities in control. Team-based home blood pressure monitoring (TB-HPBM) involving patient transmission of their home blood pressure readings in real-time to their clinical team has been shown to improve blood pressure control. There is an urgent need to implement TB-HBPM into practice. The overall objective of this research is to assess implementation strategies that mitigate barriers and leverage facilitators to TB-HBHM on hypertension control and disparities between Black and White patients. The study team and investigators will use mixed methods to assess the process and generate knowledge to facilitate broader uptake of TB-HBPM.

Detailed description

Aim 2: Deploy theorized implementation strategies using a type-2 hybrid stepped-wedge randomized cluster trial The department of family medicine will roll out the clinical intervention (TBHBPM). To improve rigor in evaluation, the study biostatistician will use computer-generated numbers to randomly assign each of the eight suites to when they will begin the intervention during one of three wedges (Figure 1). The study team and investigators will randomize two suites in the first wedge and three each to the second and third wedge. Aim 3: Assess the impact of implementation strategies using specific metrics based on RE-AIM Aim 4: Test theoretical assumptions underlying the implementation strategies

Interventions

BEHAVIORALTeam-Based Home Blood Pressure Monitoring

Implementation of best practices for hypertension control using a practice wide team-based home blood pressure monitoring intervention

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
University of Rochester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Stepped Wedge Cluster Randomized Design. Each practice suite represents a cluster. All eight suites begin in the control group and then cross over (one-way) to the intervention group at one of three randomly assigned time periods, ensuring that all suites eventually receive implementation of TB-HBPM.

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

ELIGIBILITY CRITERIA Clinicians and Staff Eligibility Criteria Practice employees (practice leaders, administrators, clinicians, or staff) that work with hypertensive patients during the study period (scheduling appointments, coordinating care, measuring blood pressure, responding to questions, and/or treating their blood pressure) Patient Inclusion Criteria * Current HFM patient 18-85 years of age with hypertension diagnosis * Diagnosis of hypertension based on ICD-10 codes of I10-I14 * at least one HFM health visit and hypertension diagnosis beginning no later than 7/1/2021. Patient

Exclusion criteria

* Not current patient in the participating practices * Diagnosis of dementia, end-stage renal disease, and/or in hospice * Currently pregnant

Design outcomes

Primary

MeasureTime frameDescription
Blood pressure controlUp to 48 months participationChange in percent of participants whose BP is controlled (defined as \<140/90 mm Hg) among all eligible patients diagnosed with hypertension based on the last BP reading during the control period and the last BP reading during the follow-up period.

Secondary

MeasureTime frameDescription
Blood pressure control by race and ethnicityUp to 48 months participationChange in percent of participants with blood pressure controlled defined as \<140/90 mm Hg by race/ethnicity: among eligible Non-Hispanic White patients, non-Hispanic Black patients, and Hispanic patients.
Blood pressure control by insuranceUp to 48 months participationChange in percent of participants with blood pressure controlled defined as \<140/90 mm Hg by insurance (Commercial, Medicaid, Medicare, Other and None)
Participation in Home Blood Pressure Monitoring (HBPM)Beginning of the intervention for the relevant wedge up to 48 months participationPercentage of participants eligible for home blood pressure monitoring (HBPM) who agree to participate in HBPM based on EHR documentation
Transmission of home blood pressure readingsFirst three months following each participant's enrollment in HBPMPercentage of participants who participate in HPBM who transmit a least 10 BP readings per month
Chronic disease self-management capacity (QICA)Pre-intervention and six months post-interventionChange in Quality Improvement Capacity Assessment QICA scores, scale range 20-200 with higher indicating better outcomes.
Sustained blood pressure controlBeginning with the 6-month intervention period and up to 48 months participationChange in percent of participants with blood pressure in control (\<140/90 mm Hg) post-intervention
Cost AnalysisUp to 48 months participationMarginal changes in net revenue (marginal billing and bonus revenue) and marginal changes in costs related to time for training, staffing costs, and BP monitor

Other

MeasureTime frameDescription
Clinician mean blood pressure (BP) goal (mm Hg) for patientsUp to 48 months participationWe will calculate the mean BP goal for each clinician based on the specified BP goal listed in EHR smartphrase for each of the clinician's patients. The mean goal is calculated by the sum of all systolic (SBP) and diastolic BP (DBP) goals divided by the number of patients with goals for each participating clinician. A reasonable range of mean BP goals are: SBP: 120-150 mm Hg and DBP: 80-100 mm Hg for different clinicians
Anti-hypertensive medication intensificationUp to 48 months participationFrequency of anti-hypertensive medication intensification (e.g., the number of additions/deletions of anti-hypertensive medication and/or number of changes in dose of anti-hypertensive medication)
The percentage of participants who are managed by a clinical pharmacistUp to 48 months participationThe percentage of HBPM participants who are managed by a clinical pharmacist based on EHR data
Team functionUp to 48 months participationChange in team function score based on the score on the TEAMS Tool scale at pre-intervention and post-intervention periods for that wedge. Scale range 14-70 with higher scores indicating better outcomes.
Exploratory outcomes- LDL control levelsUp to 48 months participationChange in LDL-cholesterol level (mg/dl) based on lipid blood testing in the EHR over 48 months.
Exploratory outcomes- Smoking statusUp to 48 months participationChange in percent of current smokers among eligible participants based on EHR documentation over 48 months.
Exploratory outcomes- Hypertension-related Emergency department visitsUp to 48 months participationChange in emergency department visits (number) involving a primary diagnosis of hypertension diagnosis among eligible patients recorded on the emergency department discharge summary from the EHR over 48 months.
Exploratory outcomes- Hypertension-related HospitalizationsUp to 48 months participationChange in hospitalization (number) involving a primary diagnosis of hypertension diagnosis among eligible patients recorded on the hospital discharge summary from the EHR over 48 months.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026