Optimizing PPI prescribing with EHR decision support

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The initiative implements alternative order-panel configurations in UCLA's CareConnect EHR, including indication-based default durations and active physician-choice prompts, to influence PPI prescribing workflows. Changes are embedded in routine practice so clinicians retain full authority to modify prescriptions. The study compares prescribing patterns across the different EHR configurations to see if defaults change behavior while monitoring for safety and workflow impact. Eligible participants are UCLA primary care physicians with at least 25% clinical full-time equivalency.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* UCLA Health primary care physicians who have a clinical full-time equivalency of at least 25%.

Exclusion Criteria:

* Physicians with a clinical full-time equivalency of less than 25%

Where it's running

• UCLA Health System
  Los Angeles, California, United States Recruiting

Study contacts

• Study coordinator: Katelyn Clinical Research Coordinator
• Email: katenguyen@mednet.ucla.edu
• Phone: 310-267-5250

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.