Actively Recruiting

Phase Not Applicable
Age: 18Years - 19Years
All Genders
Healthy Volunteers
NCT06115252

Partnering to Enhance Emerging Adults' Response to Programs

Led by UConn Health · Updated on 2026-02-10

248

Participants Needed

1

Research Sites

129 weeks

Total Duration

On this page

Sponsors

U

UConn Health

Lead Sponsor

U

University of Texas

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Partnering to Enhance Emerging Adults' Response to Programs

Who Can Participate

Age: 18Years - 19Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be within the age range of 18 to 19 years
  • Agree to be contacted for follow-up visits at 3, 6, and 12 months
  • Provide fully informed consent to participate
Not Eligible

You will not qualify if you...

  • Be left-handed
  • Have a history of brain injury, neurological or neurodevelopmental disorders including psychosis, or use related medications
  • Have experienced loss of consciousness lasting 2 minutes or more
  • Have any contraindications for fMRI such as unremovable metal in the body or being pregnant

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Texas Dallas

Dallas, Texas, United States, 75235

Actively Recruiting

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Research Team

K

Karen Hudson, MCR

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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Partnering to Enhance Emerging Adults' Response to Programs | DecenTrialz