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N/A N=2,211 Randomized Triple-blind Supportive Care

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

Heart Failure · Heart Failure With Reduced Ejection Fraction

Enrolled (actual)
2,211
Serious AEs
0.0%
Results posted
Oct 2024
Primary outcome: Primary: Number of Participants Prescribed Mineralocorticoid Receptor Antagonists (MRA) During Study — 224; 127; 75 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Best Practice Alert (BPA) (Other); In-Basket Message (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
NYU Langone Health
Primary completion
Oct 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Prescribed Mineralocorticoid Receptor Antagonists (MRA) During Study
224; 127; 75
SECONDARY
Number of Participants Prescribed to Beta-blocker (BB), Angiotensin Converting Enzyme (ACE) Inhibitor, Angiotensin Receptor Blocker (ARB), or Angiotensin Receptor/Neprilysin Inhibitor (ARNI) During Study
87; 94; 85

Summary

Building Electronic Tools To Enhance and Reinforce CArdiovascular REcommendations - Heart Failure (BETTER CARE-HF) is a pragmatic, cluster-randomized, three-arm intervention trial that will compare the effectiveness of two targeted clinical decision support (CDS) intervention tools (best practice alert (BPA) and automated in-basket massage) to inform providers when a patient with heart failure and reduce ejection fraction (HFrEF) is not on appropriate medical therapy, as compared to usual care.

Eligibility Criteria

Inclusion Criteria

  • Cardiologist visit
  • Transthoracic echocardiogram with the most recent EF >= 40%

Exclusion Criteria

  • Hypotension: SBP 5.1, or any K >5.5
  • Renal dysfunction: eGFR < 30
  • Ventricular assist device
  • Hospice care
  • Cardiac amyloid
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05275920). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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