Can telehealth bridge the gap for opioid treatment?
NCT ID NCT06341608
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study will develop and test a telehealth program designed to help marginalized patients access and stay in treatment for opioid use disorder. Researchers will enroll 60 people—half already in treatment and half not yet in treatment—and provide them with a user-friendly telehealth platform, case management, reminders, and mailed drug tests. The goal is to see if this approach improves treatment engagement and satisfaction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- telehealth intervention (behavioral)
- What this could lead to
- If successful, this could show that telehealth makes it easier for marginalized people to start and stay on opioid use disorder treatment.
- What could go wrong
- This is a small pilot study with only 60 participants, so results may not apply broadly. The intervention is still being developed, and it may not improve engagement as hoped.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2028
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.
Aim 1: Inclusion Criteria For patients: Must be 18 years old or older Clinical diagnosis of opioid use disorder and/or mental health diagnosis Must be receiving treatment for opioid use disorder and/or mental health diagnosis at an outpatient community-based substance use disorder and/or mental health treatment program Must speak English For providers and staff: Must be 18 years old or older Must be in a provider, clinical staff, or leadership role caring for patients with substance use disorders and/or mental health diagnoses Must speak English Aim 2b: Inclusion Criteria: Must be 18 years or older Clinical diagnosis of opioid use disorder Must be receiving treatment for OUD with buprenorphine at Prevention Point Philadelphia Must speak English Aim 3: Patient participants: Must be 18 years old or older Clinical diagnosis of opioid use disorder Must be currently receiving in-person disorder care with buprenorphine at Prevention Point for a duration of 1-3 months OR not currently receiving disorder treatment but approved for treatment intake at buprenorphine clinic by Prevention Point clinician Must be English speaking Provider and staff participants: Must be a provider or staff member at Prevention Point Philadelphia in the buprenorphine OUD treatment program Must be involved in the care of at least one patient enrolled in the pilot trial Must be English speaking
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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 Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
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Other studies related to the condition(s) this trial covers.
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