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Clinical Trials/NCT02794311
NCT02794311
Completed
Not Applicable

AlcoholPredict: Neuropsychology, Brain Imaging and Genetic Polymorphisms in Binge Drinking

CHU de Reims1 site in 1 country125 target enrollmentFebruary 1, 2015
ConditionsBinge Drinking

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Binge Drinking
Sponsor
CHU de Reims
Enrollment
125
Locations
1
Primary Endpoint
Neuropsychological test : Mini International Neuropsychiatric Interview (M.I.N.I)
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
February 1, 2015
End Date
September 24, 2019
Last Updated
3 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility 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)

Outcomes

Primary Outcomes

Neuropsychological test : Mini International Neuropsychiatric Interview (M.I.N.I)

Time Frame: day 1

Neuropsychological test : Wisconsin Card Sorting Test (WCST)

Time Frame: V2(3 weeks later)

Genetics tests (Single Nucleotide Polymorphism)

Time Frame: V2(3 weeks later)

MRI - signal BOLD (" Blood Oxygen Level Dependant ").

Time Frame: V3(up to 2 month)

Neuropsychological test : Family Informant Schedule and Criteria (FISC)

Time Frame: day 1

Neuropsychological test : Alcohol Use Questionnaire

Time Frame: day 1

Neuropsychological test :Trail Making Test, partie A et B

Time Frame: V3(up to 2 month)

Neuropsychological test : Plus/Minus Test

Time Frame: V3(up to 2 month)

Neuropsychological test :Go/No-Go

Time Frame: V3(up to 2 month)

Study Sites (1)

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