ClinicalTrials.Veeva

Menu

Brief Intervention to Prevent Alcohol Socialization (BIPAS Alcohol)

University of North Carolina (UNC) logo

University of North Carolina (UNC)

Status

Completed

Conditions

Drinking, Alcohol
Adolescent Behavior
Drinking Behavior
Alcohol Drinking, Adolescent

Treatments

Behavioral: BIPAS Alcohol

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05520333
22-0101
1R34AA028856-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Early alcohol socialization occurs within the family. This multi-level, high-reach, low-intensity intervention to prevent early alcohol use capitalizes on the influence of providers, immunization timing, and pediatric guidelines that advise healthcare providers to give anticipatory guidance about early alcohol use. In conjunction, the intervention capitalizes on the power of technology to reinforce and expand upon pediatrician messages.

The study seeks to understand the feasibility and effectiveness of a pilot intervention designed to prevent alcohol socialization through education of parents of rising 6th grade students.

Enrollment

132 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years or older;
  • Parent or guardian of an enrolled child at a study clinic;
  • Cohabitate part time (2 days/week) or more with enrolled child;
  • Be able to complete study activities in English;
  • Be able to give informed consent;
  • Own a phone with text message capabilities and access to internet.

Exclusion criteria

  • Families in which the 10-to-12-year old child is actively receiving treatment for alcohol use disorder.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

132 participants in 2 patient groups

Intervention arm
Experimental group
Description:
Families receive text messages for three months.
Treatment:
Behavioral: BIPAS Alcohol
Waitlist-control arm
No Intervention group
Description:
Families are randomized into a control group for three months and begin receiving text messages for three months.

Trial documents
2

Trial contacts and locations

1

Loading...

Central trial contact

Marina Pearsall, MPH; Nisha Gottfredson O'Shea, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems