Messaging to Providers About Treatment of Heart Failure at Inova
This study is looking at whether a special alert in the electronic health record (EHR) can help doctors prescribe the right medications for patients with heart failure with reduced ejection fraction (HFrEF). HFrEF means your heart's main pumping chamber doesn't squeeze as well as it should. The alert will pop up for doctors when they open your medical record, reminding them about guideline-recommended heart failure medications you might not be taking. The goal is to see if this alert leads to more patients receiving these important medications within 30 days. You could be eligible if you are over 18, have HFrEF (left ventricular ejection fraction ≤40%), and are seen by a cardiologist at an Inova clinic or hospital. The study status is currently unclear.
- Study design
- This is a randomized, single-blind study involving approximately 5000 participants. Some doctors will receive the electronic health record alert, while others will provide usual care.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will measure the use of guideline-directed medical therapy (GDMT) 30 days after randomization.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
PRagmatic Trial Of Messaging to Providers About Treatment of Heart Failure at Inova
At a glance
Conditions
NCT05433220
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Inova Health System
Falls Church, Virginiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Mitchell Psotka, MD, PhD · PRINCIPAL_INVESTIGATOR · Inova Health Care Services
Who to contact
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Inclusion
Exclusion
What this trial measures
- Increased use of GDMT in patients with Heart Failure with Reduced Ejection Fraction30 days after randomization
The primary outcome for the trial will be the proportion of patients with HFrEF who have an increase in the number of prescribed evidence-based therapies for HFrEF (beta-blockers, ACE-I/ARB/ARNI, MRA, SGLT2i) 30 days after randomization.