The overarching goal of this proposal is to integrate patient social risk information into an existing electronic health record (EHR)-based clinical decision support (CDS) tool (CDSv1) to facilitate emergency department (ED)-initiated, social risk-informed opioid use disorder (OUD) medication treatment and ultimately improve treatment adherence and follow up. The investigators will evaluate the feasibility and acceptability of the social care-enhanced CDS tool, CDSv2, (compared to CDSv1) at a single study site (UCSF) as an intervention to increase medication treatment adherence and follow up for adult ED patients experiencing opioid use disorder using a mixed-methods, before-after approach.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
CDSv1 clinician launch
Timeframe: 12 months
CDSv1 encounter launch
Timeframe: 12 months
CDSv2 clinician launch
Timeframe: 12 months
CDSv2 encounter launch
Timeframe: 12 months
CDSv1 adherence to OUD treatment recommendations
Timeframe: 12 months
CDSv2 adherence to OUD treatment recommendations
Timeframe: 12 months
CDSv2 adherence to social care recommendations
Timeframe: 12 months
CDSv1 acceptability
Timeframe: During first 6 months of CDSv1 deployment
CDSv1 appropriateness
Timeframe: During first 6 months of CDSv1 deployment
CDSv2 acceptability
Timeframe: During first 6 months of CDSv2 deployment
CDSv2 appropriateness
Timeframe: During first 6 months of CDSv2 deployment
Patient recruitment CDSv1
Timeframe: 12 months
Patient recruitment CDSv2
Timeframe: 12 months
ED clinicians' perceptions of CDSv1
Timeframe: Within first 8 months of CDSv1 deployment
ED patients' perceptions of CDSv1
Timeframe: Within first 8 months of CDSv1 deployment
ED clinicians' perceptions of CDSv2
Timeframe: Within first 8 months of CDSv2 deployment
ED patients' perceptions of CDSv2
Timeframe: Within first 8 months of CDSv2 deployment
Feasibility of primary endpoint collection for CDSv1
Timeframe: 13 months
Feasibility of primary endpoint collection for CDSv2
Timeframe: 13 months