Actively Recruiting

Phase Not Applicable
Age: 14Years - 24Years
All Genders
ID06311838

Building Social and Structural Connections for the Prevention of Opioid Use Disorder Among Youth Experiencing Homelessness: An RCT Examining Biopsychosocial Mechanisms

Led by Ohio State University · Updated on 2025-09-22

300

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Youth experiencing homelessness face many challenges including high rates of substance use and mental health disorders, which can have long-lasting effects on their well-being. This research aims to study a comprehensive prevention program that targets social factors affecting these youth to improve their health outcomes. The study uses a dismantling design to identify which parts of the intervention are most effective in reducing opioid misuse and improving mental health among homeless youth aged 14 to 24 years. Participants will be randomly assigned to one of four groups: Motivational Interviewing combined with the Community Reinforcement Approach plus usual services; Strengths-Based Outreach and Advocacy plus usual services; a combination of all three interventions; or usual services alone offered by a community drop-in center. The interventions include counseling sessions, advocacy to help meet basic needs and connect with resources, and usual drop-in center support. The study evaluates how these approaches impact opioid use disorder prevention and mental health outcomes. Youth will be assessed at the start and then again at 3, 6, 12, 18, and 24 months to monitor substance use, mental health, and overall well-being. Assessments include interviews about substance use, questionnaires for depression and anxiety, and health surveys. The study also explores how factors like age, sex, and past experiences affect responses to the interventions. Researchers will track costs to help guide future programs for homeless youth.

CONDITIONS

Brief Title

Building Social and Structural Connections for the Prevention of Opioid Use Disorder Among Youth Experiencing Homelessness

Who Can Participate

Age: 14Years - 24Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth must meet the criteria for homelessness as defined by the McKinney-Vento Act: lacking a fixed, regular, and adequate nighttime residence; or living in a welfare hotel, a place without regular sleeping accommodations, or in a shared residence due to loss of housing or economic hardship
  • Must speak English adequately to complete study measures
  • Aged between 14 and 24 years
Not Eligible

You will not qualify if you...

  • Youth who have a stable housing situation
  • Non-English speakers

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Duration varies based on intervention components

Participants receive behavioral interventions including Motivational Interviewing, Community Reinforcement Approach, and/or Strengths-Based Outreach and Advocacy depending on their assigned group. The number and frequency of sessions vary based on the intervention type and individual needs.

Multiple sessions including 2 Motivational Interviewing sessions and up to 12 Community Reinforcement Approach sessions; Strengths-Based Outreach and Advocacy sessions are flexibly scheduled based on youth needs

Follow-up Monitoring

Duration - Up to 24 months post intervention

Participants are monitored with assessments on substance use, mental health, and related outcomes at multiple time points after the intervention.

Assessments at baseline, and 3, 6, 12, 18, and 24 months post intervention

Trial Site Locations

Total: 2 locations

1

Star House

Columbus, Ohio, United States, 43201

Actively Recruiting

2

Ohio State University

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

J

Jodi Ford, PhD

N

Natasha Slesnick, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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