N/A
N=132
Brief Intervention to Prevent Alcohol Socialization (BIPAS Alcohol)
Alcohol Drinking, Adolescent · Drinking Behavior · Drinking, Alcohol · Adolescent Behavior
Bottom Line
View on ClinicalTrials.gov: NCT05520333 ↗Enrolled (actual)
132
Serious AEs
—
Results posted
Jun 2025
Primary outcome: Primary: Change in Mean Value of Parental Pro-sipping Beliefs Score — 0.13; 0.08 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- BIPAS Alcohol (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of North Carolina, Chapel Hill
- Primary completion
- Jul 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Mean Value of Parental Pro-sipping Beliefs Score |
0.13; 0.08 | — |
Summary
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.
Eligibility Criteria
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.
Data sourced from ClinicalTrials.gov (NCT05520333). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.