Your session is about to expire
← Back to Search
Best Practice Alert (BPA) for Heart Failure (BETTER CARE-HF Trial)
N/A
Waitlist Available
Led By Amrita Mukhopadhyay, MD
Research Sponsored by NYU Langone Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, 1 year
Awards & highlights
BETTER CARE-HF Trial Summary
This trial will compare the effectiveness of two targeted clinical decision support intervention tools (best practice alert and automated in-basket massage) to inform providers when a patient with heart failure and reduce ejection fraction is not on appropriate medical therapy, as compared to usual care.
Eligible Conditions
- Heart Failure
BETTER CARE-HF Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, 1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Percentage of patients prescribed MRA
Secondary outcome measures
Incidence of provider engagement with each alert type
BETTER CARE-HF Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: In-Basket Message groupExperimental Treatment1 Intervention
Providers will receive a monthly in-basket messages linking to a list of patients who have been seen in the past 2 months or will be seen in the upcoming month with HFrEF who are not on MRA (and who do not have contraindication to MRA). This list will display each patient's current hFrEF therapies, EF, blood pressure, potassium, glomerular filtration rate, date of last visit, and date of next visit. From the list, providers can access the patient's chart, order medications, and document communication with the patient.
Group II: Best Practice Alert groupExperimental Treatment1 Intervention
Providers will receive a BPA at the time of visit for patients with HFrEF who are not on MRA (and who do not have contraindication to MRA). This alert will display the patient's current HFrEF therapies, EF, blood pressure, potassium, and glomerular filtration rate. The alert will give access to an outpatient heart failure order set, and also provide links to the most recent guidelines.
Group III: Control groupActive Control1 Intervention
Patients who will receive the current standard practice of care (no BPA or in-basket message)
Find a Location
Who is running the clinical trial?
NYU Langone HealthLead Sponsor
1,368 Previous Clinical Trials
837,515 Total Patients Enrolled
15 Trials studying Heart Failure
10,767 Patients Enrolled for Heart Failure
Amrita Mukhopadhyay, MDPrincipal InvestigatorNYU Langone Health
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger