Brief Alcohol-focused Intervention for Patients in Opioid Agonist Treatment
This study is testing a brief alcohol treatment called "Brief opioid-informed alcohol treatment" for people who are taking buprenorphine for opioid use disorder and also drink alcohol. This treatment uses ideas from Motivational Enhancement Therapy (MET) and Cognitive Behavioral Therapy (CBT) to help people reduce their alcohol use. To join, you must be 18 or older, taking buprenorphine for at least two weeks, and meet criteria for alcohol use disorder, drinking at least one day a week. The study aims to see if this treatment is practical and acceptable to patients, and if it can help improve alcohol-related outcomes. The results will help decide if a larger study is needed in the future. The study plans to enroll 60 participants, but its current status is unclear.
- Study design
- This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 60 participants.
- What's involved
- Participants will attend weekly in-person sessions for four weeks.
- Compensation
- Not stated in the trial record.
- Follow-up
- The acceptability and feasibility of the treatment will be assessed at Week 4 (end of trial).
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Better Experiences in Substance Treatment: A Brief Alcohol-focused Intervention Tailored for Patients in Opioid Agonist Treatment
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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Inclusion
Exclusion
What this trial measures
- Acceptability of the treatmentAssessed at Week 4 (end of trial)
Acceptability will be assessed with the Satisfaction Questionnaire (CSQ-8), which ranges in scores from 8 to 32 (higher scores indicate higher satisfaction). Treatment satisfaction will be considered acceptable if the number and percentage of subjects who rate their treatment experience in the "satisfactory" or "highly satisfactory" range on the CSQ-8 is ≥ 80%.
- Feasibility of the treatmentAssessed at Week 4 (end of trial)
Retention feasibility will be determined by the number and percentage of enrolled participants who complete the four week treatment protocol.