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Multi-Center Project: Building Electronic Tools To Enhance and Reinforce CArdiovascular REcommendations - Heart Failure

Multi-Center Project: BETTER CARE - HF (Building Electronic Tools To Enhance and Reinforce CArdiovascular REcommendations - Heart Failure)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06457152
Acronym
BETTER CARE-HF
Enrollment
1136
Registered
2024-06-13
Start date
2025-04-04
Completion date
2026-03-29
Last updated
2026-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

This study will test an automated, electronic health record (EHR-)embedded alert to improve prescribing of guideline-directed medical therapy for patients with heart failure and reduced ejection fraction (HFrEF). The investigators have previously tested and implemented this alert at NYU Langone Health (NYULH), and will now test and implement this alert across three other health systems.

Interventions

OTHEREHR-Emedded Alert

For patients randomized to the intervention group, an automated, EHR-embedded alert will be visible in the patient's chart that promotes appropriate medical therapy for patients with HFrEF.

Sponsors

NYU Langone Health
Lead SponsorOTHER
Massachusetts General Hospital
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
OhioHealth
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patient with an encounter visit at participating cardiology practice during the study period * Patient with EF of less than or equal to 40% on most recent echocardiogram at the time of visit * Patient ages 18-90

Exclusion criteria

* Pregnancy * Ventricular assist device * Hospice * Cardiac amyloid * Medication-specific exclusion for MRA: most recent systolic blood pressure less than 105 mm Hg, most recent potassium \< 5.1, any potassium \> 5.5, most recent glomerular filtration rate \< 30 (using MDRD equation), or a documented MRA allergy.

Design outcomes

Primary

MeasureTime frameDescription
Number of Patients with a Prescription for Mineralocorticoid Antagonists (MRA)Up to Day 30Measured at the prescription encounter level using patient EHR data.

Secondary

MeasureTime frameDescription
Number of Patients with a Prescription for Beta-Blocker (BB)Up to Day 30Measured at the prescription encounter level using patient EHR data.
Number of Patients with a Prescription for ACE-I/ARB/ARNIUp to Month 36Prescription for angiotensin converting enzyme-inhibitors/angiotensin receptor blockers/angiotensin receptor neprilysin inhibitors (ACE-I/ARB/ARNI) measured at the prescription encounter level using patient EHR data.
Number of Patients with a Prescription for Sodium-Glucose Cotransporter-2 Inhibitor (SGLT2i)Up to Month 36Measured at the prescription encounter level using patient EHR data.
Number of Patients with HyperkalemiaUp to Month 36Measured using patient EHR data.
Number of Patients who are HospitalizedUp to Month 36Measured using patient EHR data.
Number of Patients who are Hospitalized for Heart Failure (HF)Up to Month 36Measured using patient EHR data.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAmrita Mukhopadhyay

NYU Langone Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 18, 2026