OUD Smartphone Services

NCT06134882 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2026-02-19

No results posted yet for this study

Summary

The purpose of the research is to check whether services and materials made available through a smartphone app are helpful to people who have been diagnosed with opioid use disorder (OUD). Participants are asked to use an app to submit videos of themselves taking salivary drug tests to a secure online system. The app includes reminders, rewards, and activities, as well as access to live support. Study participation lasts one year and includes about 30 minutes each week submitting videos, an hour-long interview to get started, and hour-long interviews once every three months after that over the course of the year.

Conditions

  • Opioid-Related Disorders
  • Drug Abuse

Interventions

BEHAVIORAL

Contingency management

Monetary incentives are delivered via reloadable debit card based on verified engagement in target behaviors, including drug abstinence, appointment attendance, and completion of self-paced cognitive behavior therapy modules.

BEHAVIORAL

Cognitive-Behavior Therapy Modules

Self-paced cognitive-behavior therapy modules delivered via smartphone.

BEHAVIORAL

Peer Contingency Management (CM) Guide

Peer supports delivered via telehealth. Support is informed by the community reinforcement approach and includes motivational interviewing

BEHAVIORAL

Drug testing

Self-performed salivary drug testing with incentives contingent upon proper completion of test procedures as confirmed by video.

BEHAVIORAL

Wellness modules

Basic health and wellness information delivered via self-paced learning modules.

BEHAVIORAL

Peer technical support

Peer support for promoting engagement and addressing technical issues delivered via a mobile digital platform.

Sponsors & Collaborators

  • DynamiCare Health Inc.

    collaborator UNKNOWN
  • RTI International

    collaborator OTHER
  • National Institute on Drug Abuse (NIDA)

    collaborator NIH
  • Western Michigan University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-23
Primary Completion
2026-05-31
Completion
2026-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06134882 on ClinicalTrials.gov