NCT04028557CompletedNot Applicable
Development and Validation of an Integrated Implementation Model for Clinical Decision Support for Heart Failure Prescribing
University of Colorado, Denver2 sites in 1 country118 target enrollmentStarted: June 24, 2019Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 118
- Locations
- 2
- Primary Endpoint
- Change in prescription of Beta blocker (BB)
Study Overview
Brief Summary
The objective of this proposal is to compare clinical outcomes, implementation metrics (i.e., patient reach and clinician adoption), and clinician preferences of two designs (customized vs. commercial) of a clinical decision support (CDS). Beta blocker prescribing for patients with heart failure will be used as a test case. The best practices in CDS design, including the user-centered design will be incorporated into the customized CDS and compared to a commercially-available CDS in the electronic health record using a cluster randomized trial.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Health Services Research
- Masking
- Single (Care Provider)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Prescribing primary care clinicians at University of Colorado Health (UCHealth) who provide care for patients with heart failure and reduced ejection fraction
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Change in prescription of Beta blocker (BB)
Time Frame: 6 months post CDS implementation
Number of prescriptions of an evidence based BB during a primary care office visit.
Secondary Outcomes
- Factors Influencing Clinician Adoption of the CDS per Qualitative Interviews(6 months post CDS implementation)
- Clinician Adoption(6 months post CDS implementation)
- Patient Reach(6 months post CDS implementation)
Investigators
Study Sites (2)
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