ClinicalTrials.gg
RecruitingNCT07278518Updated Aug 24, 2026

Evaluation of a Patient Decision Aid for Emergency Department Initiated Buprenorphine

An interventional study of Patient Decision Aid for Opioid Use Disorder in Opioid Use Disorder, sponsored by Medical University of South Carolina. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-24.

Sponsored by Medical University of South Carolina · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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).

02

Conditions studied

  • Opioid Use Disorder

Keywords

  • buprenorphine
  • patient decision aid
  • emergency department
03

In context

Opioid-Related Disorders

1,472 studies on the registry are indexed under Opioid-Related Disorders; 290 are open to participants now.

This study's planned enrollment of 20 is below the median of 63 across 1,166 interventional studies indexed under Opioid-Related Disorders.

Browse Opioid-Related Disorders studies →

Lead sponsor

Medical University of South Carolina is the lead sponsor of 874 studies on the registry; 166 are open to participants now.

Of its 131 completed or terminated interventional studies of FDA-regulated products, 104 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥18
  • 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

Exclusion Criteria:

- Prisoners

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Patient Decision Aid

    This arm will receive the patient decision aid

    Behavioral: Patient Decision Aid for Opioid Use Disorder

  • No intervention
    Treatment as Usual

    This will be treatment as usual without the patient decision aid

Interventions

  • BehavioralPatient Decision Aid for Opioid Use Disorder

    This will include information structured for patients about buprenorphine as a treatment options in the emergency department.

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What researchers measure

Primary outcomes

  1. Acceptability of Intervention Measure (AIM)

    Time frame: Day 1

Secondary outcomes

  1. Knowledge about MOUD

    This is a multiple choice knowledge quiz

    Time frame: pre and post intervention on day 1, and at 7 days

  2. Treatment selection

    Time frame: Day 1

  3. Decisional Conflict Scale

    Time frame: Day 1

  4. Receipt of buprenorphine

    Time frame: Day 1, 7

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: Yes — De-identified data will be shared via the NIDA data repository in accordance with NIH Data Management and Sharing Policy.

Supporting information: Study protocol

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2026 (actual). Primary completion is estimated for Feb 2027, 6 months after the start.

Of 464 non-industry interventional studies with no phase under Opioid-Related Disorders, half reached primary completion within 29 months of starting (the median), counting those still running; a quarter within 14 and three quarters within 47. This study's planned 6 months is below that.

Counting every sponsor, half of 495 studies reached it within 29 months; a quarter within 13 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 3, 2025
First posted
Dec 12, 2025
StartActual
Aug 13, 2026
Primary completionEst.
Feb 13, 2027
CompletionEst.
Feb 13, 2027
Last update
Aug 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07278518
Responsible party
Lindsey Jennings (Associate Professor-Faculty, Medical University of South Carolina) — Principal investigator
First posted
Dec 12, 2025
Start date
Aug 13, 2026
Primary completion
Feb 13, 2027 (estimated)
Completion
Feb 13, 2027 (estimated)
Last update
Aug 24, 2026

Study contacts

Lindsey Jennings, MD, MPH
Contact
jennil@musc.edu
(843) 876-8023
Lindsey Jennings, MD, MPH
principal investigator · Medical University of South Carolina

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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