Telehealth treatment for opioid use disorder in adults
Official title: A Randomized Clinical Trial of Telehealth Treatment for Opioid Use Disorders
Run by Yale University · NCT07362082 · Data updated 2026-11-12
This trial tests whether using the RecoveryPad telehealth platform helps adults with moderate to severe opioid use disorder.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 470 (estimated) |
| Sponsor | Yale University Academic / other |
| Locations | 1 site (New Haven, Connecticut) |
| Status | Recruiting |
| Started | September 11, 2026 |
| Main results expected | October 1, 2027 |
| Study ends | December 1, 2027 |
| Registry record updated | September 21, 2026 |
| Trial ID | NCT07362082 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with moderate to severe opioid use disorder who can use a smartphone, tablet, or computer and have an active contact email or are willing to create one, and who are not currently on buprenorphine, methadone, or naltrexone for an SUD.
✕Probably not a fit
Individuals currently on certain opioid-use medications, pregnant, at risk of suicide, or incarcerated may not benefit from this telehealth approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study evaluates a telehealth platform called RecoveryPad (RP) for adults with moderate to severe opioid use disorder. Participants will engage with RP remotely via devices that can browse the web and receive texts as part of their care. Recruitment requires English literacy, consent, a positive DSM-5 OUD screen, and access to a phone and email. Exclusion criteria include current use of certain opioid-use medications, pregnancy, suicide risk, or incarceration at enrollment. The study is led by Yale University with NIDA and collaborators, and is based at Yale in New Haven, CT.
Why it matters
Potential benefit: If successful, participants may experience improved access to treatment and support for opioid use disorder through telehealth services.
How similar studies have gone: Telehealth approaches for opioid use disorder have shown promise in improving access to care and engagement in treatment in prior studies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Can speak, read and write in English * Provision of signed and dated informed consent form * Screened positive for OUD, moderate or severe, based on the Diagnostic and Statistical Manual-5th Edition * Have a working cell phone number and working device that can access a web browser and receive texts (i.e., smartphone, tablet or computer) * Can provide a working email address OR be willing to create one Exclusion Criteria: * Current use of buprenorphine, methadone, or naltrexone for a substance use disorder * Pregnancy * Known current suicide risk based on participant self-report * On parole or incarcerated at time of enrollment based on participant self-report
Where it's running
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Yale University
New Haven, Connecticut, United States Recruiting
Study contacts
- Principal investigator: Rebekah Heckmann, MD — Yale University
- Study coordinator: Rebekah Heckmann, MD
- Email: rebekah.heckmann@yale.edu
- Phone: (203) 737-8335
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.