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Improving Hypertension Management Through Preference List Defaults

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Geisinger Health

Status

Not yet enrolling

Conditions

Quality Improvement
Hypertension
Choice Behavior
Clinical Decision Support

Treatments

Behavioral: Revising preference list by adding "(PREFERRED)" to combination medication names

Study type

Interventional

Funder types

Other

Identifiers

NCT07298694
2025-0593

Details and patient eligibility

About

This study aims to evaluate whether modifying the EPIC preference list to display combination blood pressure (BP) medications at the top and/or adding "(PREFERRED)" to the beginning of the medication listing increases prescribing of these medications. Combination BP medications are aligned with value-based care guidelines and may improve patient adherence and reduce pill burden. Currently, these medications may be under-prescribed in part due to their low visibility in the EPIC prescribing interface.

Full description

In this study, 50 primary care clinics at Geisinger will be randomized to a re-ordered preference list with combination BP medications at the top and/or adding "(PREFERRED)" to the beginning of the medication listing, or to have no change to the preference list.

This intervention works by adding a special character ( i.e., "(" ) to the beginning of a medication name in EPIC, which moves it to the top of the preference list. However, this only works when the provider searches for the first medication in a combination medication. For example, if a provider in the intervention group searches for "Amlodipine," the combination "(PREFERRED) Amlodipine-Benazepril" will appear at the top of the preference list.

However, a special character is NOT prioritized in the preference list when the second medication in a combination medication name is searched. For example, if the provider searches "Benazepril," the combination "(PREFERRED) Amlodipine-Benazepril" will be shown after single-class Benazepril prescriptions. The "(PREFERRED)" prefix will still be shown, which may encourage prescribing even without the medication listed first.

The study will employ a three-level hierarchical design, clustering patients within providers and providers within clinics. The study will run for 3 months or until enrollment reaches 12,150 unique patients, whichever comes second.

Clinic randomization will be stratified by variables that may affect response to the intervention including: clinic type (community medicine, senior medicine, internal medicine, FQHC), baseline prescribing rate for combination medications (<8%, 8%-13%, >13%), and number of providers (1-4, 5-9, 10-29, 30+).

One exception to the above stratification is internal medicine, where there are only two clinics. These are also the only two clinics with 30+ providers, but baseline combination medication prescribing rates fall in different stratification categories. These two clinics will be kept in the same stratum because they are still similar in culture, procedures, and size.

Stratified randomization was simulated 1000 times. Because strata are randomized independently and some strata include uneven numbers of clinics, overall assignment of the 50 clinics to treatment and control was uneven (e.g., 26 in treatment and 24 in control) on 709 of the 1000 iterations. To ensure a balance in clinic allocation to study arms, one of the 291 evenly randomized iterations will be randomly selected for implementation in the study.

Enrollment

12,150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Order placed for a medication starting with any of the following: "amlodipine", "benazepril", "valsartan", "lisinopril", "hctz", "hydrochlorothiazide", "hydro", "losartan"
  • The order is placed at an in-person, virtual (telemed), telephone, or nurse encounter in a clinic included in the study
  • Patient is age 18+
  • Order is placed in the clinician's primary clinic

Exclusion Criterion:

- Order was placed by a clinical leader who was aware of the study

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

12,150 participants in 2 patient groups

Revised Preference List
Experimental group
Description:
"(PREFERRED)" will be added to the beginning of the preference list for selected BP medications, which will frequently cause these medications to be listed first.
Treatment:
Behavioral: Revising preference list by adding "(PREFERRED)" to combination medication names
No Change to the Preference List
No Intervention group
Description:
Clinics will retain the usual EHR preference list order, with no changes to the default medication display.

Trial contacts and locations

0

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Central trial contact

Sasha C Brietzke, PhD; Gail M Rosenbaum, PhD

Data sourced from clinicaltrials.gov

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