Actively Recruiting
PACT Involvement in Cardiology Patients
Led by The Hospital for Sick Children · Updated on 2026-04-23
1000
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this trial is to determine the effectiveness of a machine-learning (ML) model predicting a serious cardiac event within the next three months, when compared pre- versus post-deployment, in pediatric cardiac inpatients. The main questions it aims to answer are whether deployment of the ML model: 1. Increases PACT consultation within the next three months among admissions without PACT involvement in the previous 100 days 2. Increases PACT consultation or visit within the next three months among those who experience a serious cardiac event during this period 3. Decreases time to PACT consultation or visit among those seen by PACT during this period 4. Decreases the incidence of death in the intensive care unit (ICU) 5. Increases documentation of goals of care High-risk cardiology patients will be identified by an ML model each morning. If the patient has been seen by the PACT team within the past year, the update will go to the PACT team members. If the patient hasn't been seen by the PACT team, the email will be sent to the cardiology physician in charge of the patient. This physician will decide whether a PACT consultation is necessary based on their clinical judgment. If so, a referral will be made using the usual process. Outcomes of the identified patients will be compared pre- and post-deployment.
CONDITIONS
Official Title
PACT Involvement in Cardiology Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pediatric inpatients admitted to cardiology
You will not qualify if you...
- Expected to be discharged prior to midnight on the day of admission
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
The Hospital for Sick Children
Toronto, Canada, M5G1X8
Actively Recruiting
Research Team
L
Lillian Sung, MD, PhD
CONTACT
A
Agata Wolochacz, BMSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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