Validation and Implementation Design of an Epic Systems 30-day Unplanned Readmission Risk Model
Trial Summary
What is the purpose of this trial?
This trial is testing a software tool that helps doctors identify patients who are likely to need to come back to the hospital after being discharged. The tool calculates a risk score and suggests additional care services for high-risk patients. The goal is to reduce unplanned readmissions by providing extra support to those who need it most.
Do I need to stop my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. It seems to focus on assessing a tool for identifying patients at risk of readmission, so it might not require changes to your medication.
What data supports the effectiveness of the treatment Epic 30-day unplanned readmission risk score?
The Epic 30-day unplanned readmission risk score has been shown to effectively predict which patients are at higher risk for readmission, with a predictive capability reflected in an AUC/C-statistic of 0.716-0.760 for all patients. This suggests it can help healthcare providers identify and potentially reduce unplanned readmissions by alerting them in real-time before discharge.12345
Is the Epic 30-day unplanned readmission risk score safe for humans?
Research Team
Donna Williams, MD
Principal Investigator
Wake Forest University Health Sciences
Eligibility Criteria
Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Implementation
Providers are randomly allocated to intervention or control groups, with the intervention group receiving the Epic 30-day unplanned readmission risk score in their workflow
Follow-up
Participants are monitored for the number of transitional and supportive care services (TSC) referrals and provider satisfaction with the clinical decision support tool
Treatment Details
Interventions
- Epic 30-day unplanned readmission risk score
Find a Clinic Near You
Who Is Running the Clinical Trial?
Wake Forest University Health Sciences
Lead Sponsor