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Clinical Trials/NCT07278518
NCT07278518
Recruiting
Not Applicable

CTN-0156: Pilot Development and Evaluation of a Patient Decision Aid for Emergency Department Initiated Buprenorphine

Medical University of South Carolina1 site in 1 country20 target enrollmentStarted: May 19, 2026Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
20
Locations
1
Primary Endpoint
Acceptability of Intervention Measure (AIM)

Overview

Brief Summary

This study aims to develop and pilot test a patient decision aid (PtDA) for emergency department (ED)-initiated buprenorphine treatment for opioid use disorder (OUD). The PtDA will be evaluated for acceptability, impact on patient knowledge, decisional conflict, and buprenorphine uptake compared to treatment as usual (TAU).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • DSM-5 criteria for moderate-to-severe OUD
  • Speaks and reads English
  • Not currently prescribed MOUD
  • Post-ED discharge patients with access to video/email

Exclusion Criteria

  • \- Prisoners

Arms & Interventions

Patient Decision Aid

Experimental

This arm will receive the patient decision aid

Intervention: Patient Decision Aid for Opioid Use Disorder (Behavioral)

Treatment as Usual

No Intervention

This will be treatment as usual without the patient decision aid

Outcomes

Primary Outcomes

Acceptability of Intervention Measure (AIM)

Time Frame: Day 1

Secondary Outcomes

  • Knowledge about MOUD(pre and post intervention on day 1, and at 7 days)
  • Treatment selection(Day 1)
  • Decisional Conflict Scale(Day 1)
  • Receipt of buprenorphine(Day 1, 7)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lindsey Jennings

Associate Professor-Faculty

Medical University of South Carolina

Study Sites (1)

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