Understanding and preventing binge drinking among students
Alcohol Consumption: Norms, Identities, & Motivations (ADUC-Volet 3 " Prevention ")
This study is testing different ways to help college students reduce binge drinking by understanding what influences their drinking habits.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 240 (estimated) |
| Ages | 18 Years to 30 Years |
| Sex | All |
| Sponsor | University Hospital, Caen Academic / other |
| Locations | 1 site (Caen) |
| Trial ID | NCT06447350 on ClinicalTrials.gov |
What this trial studies
This study aims to explore the factors influencing binge drinking among students and develop effective prevention strategies. It utilizes a randomized controlled trial design to validate programs that incorporate motivational interviewing, induced hypocrisy, social identity mapping, and motivational modeling. By analyzing the psychological determinants of alcohol consumption, the study seeks to create tailored interventions that resonate with young adults. The research is conducted at the University Hospital in Caen, focusing on a student population.
Who should consider this trial
Good fit: Ideal candidates for this study are students aged 18 to 30 who are French speakers and exhibit binge drinking behaviors.
Not a fit: Patients who are pregnant, breastfeeding, or have a history of certain medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more effective prevention tools for binge drinking, ultimately reducing alcohol-related harm among students.
How similar studies have performed: Other studies have shown promise in using motivational interviewing and social identity approaches for alcohol prevention, suggesting potential success for this novel intervention.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * aged between 18 and 30 years old, * of French mother language, * of both sexes, * binge drinking score \> 1, * having signed an informed consent. Exclusion Criteria: * Pregnant or breastfeeding students, * students who declare a history of neurological, neurosurgical, psychiatric, endocrine or infectious diseases.
Where this trial is running
Caen
- CAEN University Hospital — Caen, France (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.