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Technology Interventions for Youth Alcohol Use

Comparing Scalable Technology-Driven Brief Intervention Packages for Youth Alcohol Use

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05988931
Enrollment
1406
Registered
2023-08-14
Start date
2023-10-25
Completion date
2027-09-01
Last updated
2026-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Drinking

Brief summary

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.

Interventions

BEHAVIORALWeb Program + App

Youth receive a brief interactive web program made available online to prevent alcohol misuse. The parent/caregiver app addresses monitoring and skill building for parents to communicate with the child about preventing underage drinking and drug use.

BEHAVIORALWeb Program + App + Text Messages

Youth receive a brief interactive web program made available online to prevent alcohol misuse. This is followed by 8 weeks of supportive text messages. The parent/caregiver app addresses monitoring and skill building for parents to communicate with the child about preventing underage drinking and drug use.

Sponsors

University of Michigan
Lead SponsorOTHER
Patient-Centered Outcomes Research Institute
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* patients age 12-19 within the Michigan Medicine health system who had a visit within the past 2 years; and * past 12-month alcohol use; and * patient has a phone that can receive text messages

Exclusion criteria

* patients who do not understand English; or * patients deemed unable to provide informed consent due to conditions that preclude understanding of assessment or intervention content; or * parent/guardian consent is not obtained; or * another child in household already enrolled in the study; or * ongoing participation in another behavioral health research study

Design outcomes

Primary

MeasureTime frameDescription
Change in Alcohol Consumption3-, 6-, 9- and 12- months post baselineAlcohol consumption will be measured using total score on the 3-item Alcohol Use Disorders Identification Test-Consumption (AUDIT-C) which includes typical quantity and frequency, and frequency of binge drinking (# of drinks modified by age based on the NIAAA Youth Guide). Higher score indicates worse outcomes.

Secondary

MeasureTime frameDescription
Change in Alcohol Related Consequences3-, 6-, 9- and 12- months post baselineAlcohol related consequences will be measured using total score on the brief 18-item version of the Rutgers Alcohol Problem Index (RAPI). Higher score indicates worse outcomes.
Change in Other Drug Use3-, 6-, 9- and 12- months post baselineOther drug use will be measured using scores derived from National Survey on Drug Use and Health (NSDUH) survey items for illicit (e.g., cannabis, cocaine, heroin) and prescription (i.e., in any way a doctor did not direct you to use; stimulants, sedatives, and opioids) drugs misuse. Higher scores indicate worse outcomes.
Change in Other Drug Use Consequences3-, 6-, 9- and 12- months post baselineOther drug use consequences will be measured using total score on an 18-item version of the drug-focused RAPI. Higher score indicates worse outcomes.
Change in Depression Symptoms3-, 6-, 9- and 12-month post baselineDepressive symptoms will be measured using the Patient Health Questionnaire-2 (PHQ-2). Higher scores indicate worse outcomes, with a score of ≥ 3 indicating a positive depression screen.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMaureen Walton, MPH, PhD

University of Michigan

PRINCIPAL_INVESTIGATORErin Bonar, PhD

University of Michigan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 29, 2026