Risk Factors Associated With Binge Drinking Behaviors Among College Students (AlcoolPredict)

CHU de Reims

Status: Completed

Conditions: Binge Drinking

Treatments: Other: Alcoolpredict

Study type: Interventional

Funder types: Other

Identifiers

NCT02794311

PO13129

Details and patient eligibility

About

The purpose of this study is to specify the psychological, cognitive, neuro-functional and genetic profile associated with binge drinker behaviors among young adults. Results will help identifying more precisely vulnerability factors associated with this pattern of alcohol consumption and guiding prevention efforts.

Full description

Binge drinking behavior is characterised by speed of drinking on a particular occasion, frequency of drunkenness during the most recent six month period, and the percentage of times getting drunk when drinking. The prevalence of weekly binge drinking among European Union drinkers in 2009 was reported to be 28% of the student population, and 33% among all young people aged 15-24. The consequences of this behavior are multiple and often dramatic, they include: academic failure, violent acts, rape, domestic or road accidents. The study aims to identify vulnerability factors associated with binge drinking. The protocol explores the psychological (personality), neuropsychological (executive functions, memory), genetic (snp polymorphisms) and neuro-anatomical (fMRI) patterns associated with binge drinking behavior.

Enrollment: 125 patients

Sex: All

Ages: 18 to 25 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

• Males or females
• Right-handed
• Aged 18-25 years
• Native French speaker, able to read French and complete study evaluations
• Caucasian
• Able to provide informed written and verbal consent

Exclusion criteria

• A significant general medical illness, including neurological disorders, mental retardation or head trauma
• Depression, bipolar disorder, schizophrenia or schizoaffective disorder diagnostic according to DSM-IV
• Handling of psychotropics substances
• A sensorial impairment (visual and/or hearing)
• Women who are pregnant
• Contraindication to the use of MRI (pacemaker, metal in their body)

Trial design

Primary purpose: Health Services Research

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)