Actively Recruiting
Optimizing Heart Failure Therapies Among Patients With Limited Access in Denver
Led by Denver Health and Hospital Authority · Updated on 2026-02-27
40
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
Sponsors
D
Denver Health and Hospital Authority
Lead Sponsor
C
Colorado Clinical & Translational Sciences Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
Numerous pharmacotherapies have been proven to reduce mortality and hospitalization rates for heart failure with reduced ejection fraction (HFrEF) patients. However, these are underutilized clinically, preventing realization of proven benefits. Simplified patient education tools and multidisciplinary teams including pharmacists have been used to improve medication optimization but in predominantly private payer groups. This study will translate these evidence-based interventions to patients with limited access to care. In this randomized, prospective study, patients with HFrEF at a local hospital dedicated to care for participants with limited access will receive either pharmacist-directed medication adjustment visits with patient education materials or standard of care. This study will assess the hypothesis that the implementation of the intervention is feasible in this population, as demonstrated by the number of visits and proportion of visits with medication adjustments. Further, medication dosing in each arm will be evaluated via the Kansas City Medication Optimization (KCMO) score, which will average the percentage of maximal doses of appropriate HFrEF medication classes a patient is on. The change in KCMO scores over the course of the pilot in the two arms will then be compared to assess the hypothesis that the intervention will better increase patients' KCMO scores than the standard of care. The findings of this study will help address knowledge gaps in the care of patients not well represented previously in the literature. This proposal addresses the translational science roadblock of recruitment and engagement of participants with limited access to care.
CONDITIONS
Official Title
Optimizing Heart Failure Therapies Among Patients With Limited Access in Denver
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 63; 18 years
- Diagnosis of HFrEF (EF 64; 40%)
- Receiving care within DHHA system
You will not qualify if you...
- Estimated glomerular filtration rate (eGFR) < 25 mL/min/1.73 m8 or receiving dialysis
- Cirrhosis
- Inability to consent
- Non-English or non-Spanish speaking
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Denver Health and Hospital Authority
Denver, Colorado, United States, 80220
Actively Recruiting
Research Team
R
Ryan C Martin, MD, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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