ACTIVE_NOT_RECRUITING

Mobile Peer Support for OUD Recovery

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The COVID-19 pandemic puts individuals recovering from opioid use disorders (OUDs), an already vulnerable population, at increased risk of overdose due to decreased access to treatment, decreased social support, and increased psychosocial stress. This proposal will test the efficacy of a promising mobile app-based peer support program, compared to usual care, in increasing recovery capital, improving retention in treatment, and reducing psychosocial adverse effects, among a national sample of people in recovery from OUD. If effective, it would provide an accessible, personalized, and scalable approach to OUD recovery increasingly needed during the COVID-19 pandemic.

Official Title

Increasing Peer Support for OUD Recovery During COVID-19 Through Digital Health: A National Randomized Controlled Trial

Quick Facts

Study Start:2022-05-12
Study Completion:2027-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05405712

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * English-speaking
  2. * Age ≥ 18 years old
  3. * Own their own smartphone
  4. * Self-identifying as being in recovery from or treatment for an opioid use disorder
  1. * Does not have an Android or iOS platform smartphone
  2. * Previous enrollment in the study
  3. * Currently incarcerated
  4. * Unable to provide informed consent

Contacts and Locations

Principal Investigator

Megan Ranney, MD, MPH
PRINCIPAL_INVESTIGATOR
Brown University

Study Locations (Sites)

Indiana University
Indianapolis, Indiana, 46202
United States
Brown University School of Public Health
Providence, Rhode Island, 02903
United States

Collaborators and Investigators

Sponsor: Brown University

  • Megan Ranney, MD, MPH, PRINCIPAL_INVESTIGATOR, Brown University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-05-12
Study Completion Date2027-03

Study Record Updates

Study Start Date2022-05-12
Study Completion Date2027-03

Terms related to this study

Keywords Provided by Researchers

  • drug overdose
  • substance-related disorders
  • chemically-induces disorders
  • Fentanyl
  • Analgesics, opioid
  • Narcotics
  • Naloxone
  • Central Nervous System Depressants
  • Physiological Effects of Drugs
  • Medications for Opioid Use Disorder
  • Recovery
  • Application
  • Machine-learning
  • Mobile treatment
  • Natural language processing
  • Opioid use disorder
  • Peer support
  • Technology

Additional Relevant MeSH Terms

  • Opioid Use Disorder