Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05897788

Text-Messaging Telehealth and Contingency Management for Opioid Use Disorder Treatment Engagement

Led by University of Pennsylvania · Updated on 2025-08-12

1808

Participants Needed

1

Research Sites

140 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

There is growing recognition of the need for approaches to initiate treatment wherever patients touch the health care system, including the Emergency Department (ED). Most research has focused on initiation of medications for opioid use disorder (MOUDs) in the ED rather than ensuring continued treatment post-discharge. The investigators propose to adapt evidence-based interventions to support patients' complex needs and facilitate continued treatment, rather than discharging them and having them navigate outpatient treatment systems with limited support. The research team will randomize participants into 1 of 4 arms to receive varying degrees of augmented usual care, including daily check-ins and contingency management. The investigators plan to examine the effects of check-ins and contingency management on engagement with addiction treatment and equity of treatment effects among racial and ethnic subgroups and assess important moderators of treatment effects.

CONDITIONS

Official Title

Text-Messaging Telehealth and Contingency Management for Opioid Use Disorder Treatment Engagement

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must be 18 or older
  • Screen positive for Opioid Use Disorder
  • Have a bridge buprenorphine prescription from ED discharge or bridge clinic
  • Able to read English
  • Have a mobile phone capable of receiving text messages
Not Eligible

You will not qualify if you...

  • Not meeting the inclusion requirements listed above

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

A

Arielle Berk

CONTACT

H

Hannah Dart, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

4

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