A new approach to bridge the gap: can personalized education boost opioid treatment uptake?
NCT ID NCT07780097
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This pilot trial tests a program called TRTME, designed to help hospitalized patients with opioid use disorder begin medication treatment after discharge. The program includes personalized education to correct misconceptions about MOUD, feedback on individual overdose risk factors, and testimonial videos. Researchers will see if participants are more likely to enroll in outpatient MOUD within 30 days and whether their knowledge about MOUD improves.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A behavioral intervention called TRTME, which includes personalized education about MOUD, tailored overdose risk feedback, and testimonial videos.
- What this could lead to
- If effective, this approach could help more people with opioid use disorder start and stay on medication treatment after a hospital stay, potentially reducing overdose risk.
- What could go wrong
- This is a small pilot study, so results may not apply broadly. The intervention's success depends on patient engagement and follow-through, which can be challenging.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. 18 years of age or older; 2. A good candidate for methadone or buprenorphine treatment according to a member of the UCMC Addiction Consult Team Exclusion Criteria: 1. Have a current planned discharge to a nursing facility 2. be currently in jail, prison, or any inpatient overnight facility as required by court of law or have pending legal action with high probability of incarceration or court-mandated inpatient treatment 3. Unable to demonstrate adequate understanding of study procedures during the consent process
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Cincinnati Addiction Sciences Division
RECRUITINGCincinnati, Ohio, 45229, United States
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Other studies related to the condition(s) this trial covers.
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- Digital toolkit aims to empower families in the opioid crisis
- Can a monthly shot beat daily pills for fentanyl users?