Evaluation of an EMR-Based Clinical Decision Support Tool for the Implementation of Guideline-Directed Therapies for Prevention of Heart Failure Among High-Risk Patients With Type 2 Diabetes

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Type 2 diabetes mellitus (T2DM) is an independent risk factor for heart failure (HF) and is associated with significant morbidity and mortality. Recent therapeutic advances in pharmacotherapies, such as sodium-glucose cotransporter-2 inhibitors (SGLT2i), have shown to be beneficial in preventing HF among patients with T2DM. However, despite widely available risk prediction and stratification tools and evidence-based practice guidelines, SGLT-2i medications are under-prescribed in the United States. The proposed study is a pragmatic, single-center, randomized trial to test the feasibility and effectiveness of a clinical decision support (CDS) tool to alert providers and improve HF risk stratification in patients with T2DM.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: No
View:

• Providers in a General Internal Medicine outpatient clinic encounter

• Providers in a subspecialty Internal Medicine outpatient clinic encounter

• Providers in family medicine outpatient clinic encounter

Locations
United States
Texas
University of Texas Southwestern Medical Center
Recruiting
Dallas
Contact Information
Primary
Ambarish Pandey, MD, MSCS
Ambarish.Pandey@UTSouthwestern.edu
214-645-2101
Time Frame
Start Date: March 25, 2021
Estimated Completion Date: October 2022
Participants
Target number of participants: 1500
Treatments
Experimental: Electronic Alert
Each provider in the alert group will receive an on-screen notification regarding the patient's increased risk of HF in diabetes and the lack of an active order for SGLT2i therapy.
No Intervention: No Alert
The CDS will not issue an on-screen alert.
Sponsors
Leads: University of Texas Southwestern Medical Center

This content was sourced from clinicaltrials.gov

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