Cardiac Rehab Referral Nudges
1 other identifier
observational
7,000
1 country
1
Brief Summary
Investigators will evaluate the effectiveness of two different EHR-embedded nudges to improve referral to cardiac rehabilitation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 19, 2026
CompletedFirst Posted
Study publicly available on registry
May 26, 2026
CompletedStudy Start
First participant enrolled
June 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 15, 2026
May 26, 2026
May 1, 2026
3 months
May 19, 2026
May 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Percentage of patients eligible for cardiac rehab referral who are referred for cardiac rehab
Baseline
Secondary Outcomes (1)
Percentage of patients who attend cardiac rehab
Day 1
Study Arms (2)
EHR Nudges
Two electronic health record (EHR)-embedded nudges will be deployed: 1) an auto pended bot order for cardiac rehab referral, 2) an EHR-embedded alert prompting cardiac rehab referral.
Usual Care
Participants in the control group will not receive the auto pended bot order or the alert.
Interventions
Two types of nudges: 1) an auto pended bot order for cardiac rehab referral, 2) an EHR-embedded alert prompting cardiac rehab referral
Eligibility Criteria
Patients seen by a cardiology provider in the ambulatory setting.
You may qualify if:
- Age of at least 18 years
- History of Coronary Artery Bypass Grafting (CABG), Percutaneous Coronary Intervention (PCI), or valve repair/replacement in the past year
You may not qualify if:
- Hospice
- Active home health
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
NYU Langone Health
New York, New York, 10016, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Amrita Mukhopadhyay
NYU Langone Health
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 19, 2026
First Posted
May 26, 2026
Study Start
June 15, 2026
Primary Completion (Estimated)
September 15, 2026
Study Completion (Estimated)
December 15, 2026
Last Updated
May 26, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
This is a quality improvement (QI) project and individual participant data (IPD) will not be shared with other researchers.