Partnering to Enhance Emerging Adults' Response to Programs
NCT ID: NCT06115252
Last Updated: 2025-11-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
248 participants
INTERVENTIONAL
2025-10-10
2028-03-31
Brief Summary
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Eligible youth will be invited to come in for a "Participation Day," during which they and a peer will independently complete questionnaires. With a peer, they will then complete a short health program, and undergo a brain scan (fMRI) while completing activities. Our study team will reach out to each participant individually again 3, 6, and 12 months later to learn about health behaviors over time.
Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Motivational Interviewing (MI)
Motivational Interviewing (MI)
Motivational interviewing with peer dyads starts with an open-ended exploration of the dyad's hazardous drinking behavior via personal stories about alcohol use. It includes a values clarification task and age-matched norms along with personalized feedback regarding the dyad's alcohol use. The goal of the session is to engage the dyad in a thoughtful conversation about drinking and the implications it may have on their lives, with an eye to bolstering and supporting inherent drive for behavior change.
Interventions
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Motivational Interviewing (MI)
Motivational interviewing with peer dyads starts with an open-ended exploration of the dyad's hazardous drinking behavior via personal stories about alcohol use. It includes a values clarification task and age-matched norms along with personalized feedback regarding the dyad's alcohol use. The goal of the session is to engage the dyad in a thoughtful conversation about drinking and the implications it may have on their lives, with an eye to bolstering and supporting inherent drive for behavior change.
Eligibility Criteria
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Inclusion Criteria
* agree to be contacted for the 3, 6, and 12 month follow ups
* provide fully informed consent
Exclusion Criteria
* evidence of brain injury/illness and/or neurological, neurodevelopmental disorder including psychosis and related medications (e.g., antipsychotics; neuroleptics)
* loss of consciousness ≥ 2 minutes
* other fMRI contraindications (e.g., unremovable metal on/in body, pregnant)
18 Years
19 Years
ALL
Yes
Sponsors
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University of Texas
OTHER
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
NIH
UConn Health
OTHER
Responsible Party
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Sarah Feldstein Ewing
Professor
Principal Investigators
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Sarah W. Feldstein Ewing, PhD
Role: PRINCIPAL_INVESTIGATOR
UConn Health
Francesca Filbey, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Texas
Locations
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University of Texas Dallas
Dallas, Texas, United States
Countries
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Central Contacts
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Facility Contacts
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Cameron Sullins, BS
Role: primary
Other Identifiers
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O25-013-1
Identifier Type: -
Identifier Source: org_study_id