About this trial
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.
Eligibility criteria
Qualifiers
All University of California, San Francisco ED providers (residents, attendings, advanced practice providers) who have used either CDSv1 or CDSv2 will be eligible to participate in surveys and interviews regarding feasibility and acceptability.
English-speaking patients ≥18 years of age presenting to the UCSF ED with opioid use disorder who receive medication treatment (as a result of CDSv1 or CDSv2) will be eligible to participate.
Disqualifiers
they have a medical or psychiatric condition requiring hospitalization at the index ED visit,
are actively suicidal, are cognitively impaired,
present from an extended care facility, or
require opioids for a pain condition.
Trial design
Treatments tested in this trial
- ED-Based Clinical Decision Support for Opioid Use Disorder
- Social Care-Enhanced Clinical Decision Support for Opioid Use Disorder
Treatment groups
Sponsors and collaborators
University of California, San Francisco
Lead sponsor
National Institute on Drug Abuse (NIDA)
Collaborator