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Clinical Trials/NCT06115252
NCT06115252
Recruiting
N/A

Partnering to Enhance Emerging Adults' Response to Programs (PEER)

UConn Health1 site in 1 country248 target enrollmentOctober 10, 2025

Overview

Phase
N/A
Intervention
Motivational Interviewing (MI)
Conditions
Alcohol Use, Unspecified
Sponsor
UConn Health
Enrollment
248
Locations
1
Primary Endpoint
Blood oxygen level dependent (BOLD) response synchrony
Status
Recruiting
Last Updated
2 months ago

Overview

Brief Summary

The goal of this clinical trial (CT) is to learn more about emerging adults' and their peers. Here, we will see how co-participating with a peer in health program might impact brain and behavior change over time.

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.

Registry
clinicaltrials.gov
Start Date
October 10, 2025
End Date
March 31, 2028
Last Updated
2 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sarah Feldstein Ewing

Professor

UConn Health

Eligibility Criteria

Inclusion Criteria

  • within the specified age range
  • agree to be contacted for the 3, 6, and 12 month follow ups
  • provide fully informed consent

Exclusion Criteria

  • left-handed
  • 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)

Arms & Interventions

Motivational Interviewing (MI)

Intervention: Motivational Interviewing (MI)

Outcomes

Primary Outcomes

Blood oxygen level dependent (BOLD) response synchrony

Time Frame: Baseline

Mean BOLD time series will be obtained for each region of interest (ROI) during peer-directed change talk trials and temporally aligned across dyad participants. Inter-brain synchrony will be quantified using z-transformed GLM β-weights within ROIs between the BOLD time series of dyad members.

BOLD response synchrony association with behavior change (past month alcohol use days)

Time Frame: 12 Months

Pearson correlation coefficients (r) of Primary Outcome #1 (ROI z-scores representing BOLD response synchrony) with individual Timeline Followback (TLFB) past month drinking days at 12 month follow up.

Secondary Outcomes

  • BOLD response synchrony association with behavior change (past month alcohol use days)(3 Months)
  • BOLD response synchrony association with behavior change (past month alcohol use days)(6 Months)

Study Sites (1)

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