RECRUITING

Following Outcomes Remotely Within Addiction Recovery Domains

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 aim of this study is to describe outcome of people with opioid use disorder over the long-term by collecting monthly and yearly data on their recovery. Adults with opioid use disorder who participate will complete surveys monthly online and once per year by phone about their substance use, mental health, treatment involvement and functioning. The goal of this study is to better understand how people with opioid use disorder recover over time to improve intervention for this group.

Official Title

CTN-0126 Following Outcomes Remotely Within Addiction Recovery Domains

Quick Facts

Study Start:2023-09-02
Study Completion:2027-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06001437

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:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Be an enrolled participant in one of two applicable clinical trials and be no longer than 24 months after the final expected assessment for that trial.
  2. 2. Be willing and able to provide locator information for survey distribution (mobile number and/or email address).
  3. 3. Be willing to allow the linkage of prior clinical trial study data to the current study record.
  1. 1. Unable to understand or communicate to complete consent or study assessments.
  2. 2. Are currently in jail, prison or other overnight facility as required by court of law or have pending legal action that could prevent participation in study activities.
  3. 3. Other factors that would cause harm or increased risk to the participant or close contacts or preclude the participant's full adherence with or completion of the study.

Contacts and Locations

Study Contact

Rebecca McHugh
CONTACT
617-855-2000
kmchugh@mclean.harvard.edu

Study Locations (Sites)

McLean Hospital
Belmont, Massachusetts, 02478
United States

Collaborators and Investigators

Sponsor: Mclean Hospital

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 Date2023-09-02
Study Completion Date2027-07

Study Record Updates

Study Start Date2023-09-02
Study Completion Date2027-07

Terms related to this study

Additional Relevant MeSH Terms

  • Opioid Use Disorder