Randomized Controlled Trial of Alert-Based Computerized Decision Support for Patients With Peripheral Artery Disease Not Prescribed Lipid-Lowering Therapy
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Brigham and Women's Hospital
- Study ID
- NCT06300450
- Status
- Recruiting
Conditions
- Dyslipidemias
- Peripheral Artery Disease
- Peripheral Vascular Diseases
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Computer Alert — BEHAVIORALOn-screen alert-based decision support raising awareness of need for lipid-lowering therapy in patients with peripheral artery disease
Study Details
This single-center, 400-patient, randomized controlled trial assesses the impact of a patient- and provider-facing EPIC Best Practice Advisory (BPA; alert-based computerized decision support tool) to increase guideline-directed utilization of statin and statin-alternative oral LDL-C lowering therapies in patients with PAD who are not being prescribed LDL-C-lowering therapy.
Key Dates
- Start date
- Mar 1, 2023
- Status verified
- Sep 2025
- Primary completion
- Feb 28, 2026
- Completion
- Jul 30, 2026
Study Design
- Enrollment
- 400 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: AlertAlert-based CDS will consist of an on-screen electronic alert that will notify the clinician that the patient has an indication for LDL-C-lowering therapy but is not prescribed any. The clinician will have the opportunity to proceed to an order template through which appropriate lipid-lowering can be prescribed. The clinician could also elect to learn more about current evidence-based recommendations for LDL-C lowering in the PAD population. Finally, the clinician could elect to proceed without ordering oral LDL-C-lowering therapy or reading evidence-based recommendations for LDL-C lowering but would have to provide a rationale for not doing so.
- No Intervention: No AlertNo on-screen notification will be issued to the clinician
Primary Outcome Measure
Frequency of prescription of oral LDL-C-lowering therapy [ Time Frame: 90 days ]
Central Contacts
- Gregory Piazza6177326984
- Candrika D Kharaini6177326984cdkhairani@@bwh.harvard.edu
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Brigham and Women's Hospital | Boston | Massachusetts | 02115 | Gregory Piazza, MD, MS (PRINCIPAL_INVESTIGATOR) Samuel Goldhaber, MD (SUB_INVESTIGATOR) Ron Blankstein, MD (SUB_INVESTIGATOR) Jorge Plutzky, MD (SUB_INVESTIGATOR) |
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