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A Clinical Trial of Telehealth Treatment for Opioid Use Disorders

A Randomized Clinical Trial of Telehealth Treatment for Opioid Use Disorders

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07362082
Enrollment
470
Registered
2026-01-23
Start date
2026-08-15
Completion date
2027-12-01
Last updated
2026-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Use Disorder

Brief summary

This trial will assess effects of enrollment in a comprehensive telehealth platform, RecoveryPad (RP), in adults with moderate or severe opioid use disorder.

Interventions

DEVICERecoveryPad platform

Telehealth platform to enhance motivation and engagement in treatment for OUD

Sponsors

Yale University
Lead SponsorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
City University of New York, School of Public Health
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Attendance for MOUDUp to 30 daysOverall attendance will be measured by attendance (yes or no) at the first MOUD appointment within 30 days of enrollment.

Secondary

MeasureTime frameDescription
Attendance for MOUDUp to 90 daysOverall attendance will be measured by attendance (yes or no) at the first MOUD appointment within 31 to 90 days of enrollment.
Engagement with MOUDUp to 90 daysEngagement will be measured by demonstrated maintained attendance with MOUD treatment within 90 days of enrollment.
Overdose Events at 30 DaysUp to 30 daysA self-report of the number of subsequent overdose events within 30 days.
Overdose Events at 90 DaysUp to 90 daysA self-report of the number of subsequent overdose events within 90 days.

Countries

United States

Contacts

CONTACTRebekah Heckmann, MD
rebekah.heckmann@yale.edu(203) 737-8335
PRINCIPAL_INVESTIGATORRebekah Heckmann, MD

Yale University

PRINCIPAL_INVESTIGATORNasim Sabounchi, PhD

CUNY Graduate School of Public Health & Health Policy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 28, 2026