Can AI and peer support close the opioid treatment gap?
NCT ID NCT06569667
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
This trial tests whether an AI-driven texting tool, combined with support from peer recovery coaches, can help Black and Latinx people who use opioids start buprenorphine treatment in primary care. Participants are enrolled from emergency departments and receive text messages with social services information, stigma reduction, and patient navigation. The study measures how many people link to opioid use disorder services and stay in treatment over a year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AI-driven texting tool combined with peer recovery coach support
- What this could lead to
- If effective, this approach could reduce racial disparities in opioid treatment access and help more Black and Latinx individuals start and stay on buprenorphine.
- What could go wrong
- The trial is small and early, so results may not apply broadly. The intervention depends on participants engaging with texts and coaches, which may not work for everyone.
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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94 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Aug 2025
- 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 to 99 years
- 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; 2. fluent in English and/or Spanish; 3. self-reported non-prescription opioid use \<30 days prior to consent; 4. provision of informed consent; 5. planned stay in NYC ≥12 month; 6. self-identified Black and/or Latinx race/ethnicity; 7. positive urine toxicology for opioids per EMR records; 8. diagnosis of OUD per the Diagnostic and Statistical Manual of Mental Disorders-5 9. self-reported interest in initiating buprenorphine in primary care 10. must have a mobile phone data plan. Exclusion Criteria: 1. inability to comprehend text content written at a 3rd grade reading level; 2. physical or visual disability preventing mobile phone use; 3. self-reported receipt of medications for OUD in past 30 days.
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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.
Contacts and locations
Locations
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NYC Health + Hospitals
The Bronx, New York, 10451, United States
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Other studies related to the condition(s) this trial covers.
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