Actively Recruiting
Using Clinical Decision Support to Provide Social Risk-Informed Care for Opioid Use Disorder in the Emergency Department
Led by University of California, San Francisco · Updated on 2025-05-07
300
Participants Needed
1
Research Sites
114 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Using Clinical Decision Support to Provide Social Risk-Informed Care for Opioid Use Disorder in the Emergency Department
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All University of California, San Francisco ED providers (residents, attendings, advanced practice providers) who have used either CDSv1 or CDSv2 can participate in surveys and interviews.
- English-speaking patients 18 years or older presenting to the UCSF ED with opioid use disorder who receive medication treatment through CDSv1 or CDSv2 can participate.
You will not qualify if you...
- Participants requiring hospitalization at the index ED visit due to medical or psychiatric conditions.
- Participants who are actively suicidal.
- Participants who are cognitively impaired.
- Participants presenting from an extended care facility.
- Participants requiring opioids for a pain condition.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of California, San Francisco
San Francisco, California, United States, 94143
Actively Recruiting
Research Team
M
Melanie F Molina, MD, MAS
CONTACT
J
Jacob Perez
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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