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Clinical Trials/NCT04028557
NCT04028557
Completed
N/A

Development and Validation of an Integrated Implementation Model for Clinical Decision Support for Heart Failure Prescribing

University of Colorado, Denver1 site in 1 country118 target enrollmentJune 24, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Decision Support Systems, Clinical
Sponsor
University of Colorado, Denver
Enrollment
118
Locations
1
Primary Endpoint
Change in prescription of Beta blocker (BB)
Status
Completed
Last Updated
3 years ago

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.

Registry
clinicaltrials.gov
Start Date
June 24, 2019
End Date
September 23, 2019
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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)

Study Sites (1)

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