Actively Recruiting
Following Outcomes Remotely Within Addiction Recovery Domains
Led by Mclean Hospital · Updated on 2025-05-13
1600
Participants Needed
1
Research Sites
147 weeks
Total Duration
On this page
Sponsors
M
Mclean Hospital
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Following Outcomes Remotely Within Addiction Recovery Domains
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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.
- Be willing and able to provide locator information for survey distribution (mobile number and/or email address).
- Be willing to allow the linkage of prior clinical trial study data to the current study record.
You will not qualify if you...
- Unable to understand or communicate to complete consent or study assessments.
- 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.
- 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.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
McLean Hospital
Belmont, Massachusetts, United States, 02478
Actively Recruiting
Research Team
R
Rebecca McHugh
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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