Actively Recruiting

Phase Not Applicable
Age: 12Years - 19Years
All Genders
NCT05988931

Technology Interventions for Youth Alcohol Use

Led by University of Michigan · Updated on 2025-10-15

1400

Participants Needed

1

Research Sites

201 weeks

Total Duration

On this page

Sponsors

U

University of Michigan

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate the effects of two programs to prevent/reduce alcohol misuse among youth primary care patients. Depending on their study condition, youth will receive a brief web-based computer program or the web program + 8 weeks of supportive text messages. Parents/caregivers of youth are encouraged to use a freely available app to guide conversations with their child about drinking. This study will have significant impact by evaluating response to these scalable interventions which can be deployed widely in clinical care settings.

CONDITIONS

Official Title

Technology Interventions for Youth Alcohol Use

Who Can Participate

Age: 12Years - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 12 to 19 within the Michigan Medicine health system who had a visit within the past 2 years
  • Past 12-month alcohol use
  • Patient has a phone that can receive text messages
Not Eligible

You will not qualify if you...

  • Patients who do not understand English
  • Patients unable to provide informed consent due to conditions that affect understanding of assessment or intervention
  • Parent or guardian consent is not obtained
  • Another child in the household is already enrolled in the study
  • Ongoing participation in another behavioral health research study

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 Michigan

Ann Arbor, Michigan, United States, 48109

Actively Recruiting

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Research Team

M

Meredith Kotov

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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