ClinicalTrials.Veeva

Menu

Personalizing Intervention to Reduce Clinical Inertia in the Treatment of Hypertension

Mass General Brigham logo

Mass General Brigham

Status

Completed

Conditions

Hypertension

Treatments

Behavioral: Audit and Feedback
Behavioral: Pharmacist E-Detailing

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04603560
2020P002897
P30AG064199 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This is a three-arm pragmatic randomized controlled trial to test two interventions targeting clinical inertia in hypertension compared to control, followed by predictive modeling to identify factors that are associated with intervention responsiveness. Study investigators will use EHR data to identify providers of patients whose hypertension treatment was not intensified. Primary care physicians will then be randomized to one of three arms: pharmacist e-detailing, provider dashboards, or no intervention (control). After the intervention, the investigators will conduct virtual interviews with select providers from each arm. A predictive modeling approach will then be used to identify patient and provider characteristics that are associated with inertia and with responsiveness to each intervention.

Full description

We propose a pragmatic randomized controlled trial to test two interventions targeting clinical inertia in hypertension compared to control, followed by predictive modeling to identify factors that are associated with intervention responsiveness.

For Aim 1, we will use Electronic Health Record (EHR) data to identify physicians of patients whose hypertension treatment was not intensified despite their having persistently elevated blood pressure. We will then randomize primary care physicians to on of three arms: academic e-detailing, social norming, or no intervention (control).

For Aim 2, we will conduct interviews with select physicians from each arm. We will then identify patient and physician characteristics that are associated with inertia and with responsiveness to each intervention.

Enrollment

511 patients

Sex

All

Ages

18 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Provider Inclusion Criteria:

  • Primary care physician
  • Practicing in primary care at Massachusetts General Hospital
  • Caring for at least 2 patients: (1) aged 18-79, (2) for whom the recent BP history in the last 18 months is above goal, (3) whose most recent BP at an outpatient visit was above goal, and (4) who did not have their hypertension treatment regimens intensified (dose increase, new medication, or medication exchange) at or since that time. The BP goal will be <140/90 for all patients. To accommodate changes in care delivery that occurred during the COVID surge, outpatient visits will include in-office and virtual visits that had vitals recorded in the EHR the same day.

Provider Exclusion Criteria:

  • fewer than 100 patients on their primary care panel
  • practice less than one session per week

Patient Inclusion Criteria:

  • had a blood pressure greater than 140/90 mmHg at 2+ PCP visits in the past 12 months
  • treatment was not intensified at any of these visits

Patient Exclusion Criteria:

  • excluded from the hypertension registry
  • currently pregnant or post-partum 6 months
  • receiving hospice care

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

511 participants in 3 patient groups

Audit and Feedback
Experimental group
Description:
A report of the provider's hypertension control rates compared to benchmark will be displayed using principles of social norming. We will present that provider's hypertension control rates compared to the 90th percentile of their peers.
Treatment:
Behavioral: Audit and Feedback
Pharmacist E-Detailing
Experimental group
Description:
A pharmacist will review the chart in advance and provide a personalized recommendation for how to intensify the specific patient's antihypertensive regimen based on current guidelines. For example, they might recommend adding an additional medication based on the patient's comorbid conditions and could suggest a starting dose and timeframe for dose escalation.
Treatment:
Behavioral: Pharmacist E-Detailing
Control
No Intervention group
Description:
No intervention will be provided to physicians in the control arm.

Trial documents
2

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems