ISRCTN10111467CompletedNot Applicable
Efficacy of brief interventions (BI) for binge drinkers
Brain and Mind Foundation (Fundacion Cerebro y Mente) (Spain)0 sites752 target enrollmentStarted: August 21, 2008Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 752
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •All adults patients aged 18 to 65 years of age will be asked to undergo alcohol use disorders screening (Alcohol Use Disorders Identification Test [AUDIT]) (Rubio et al., 1998) by their primary care physicians (PCPh). All patients who screen positive will be contacted and invited to participate in a face-to-face interview to determine their eligibility for the trial. Patients will be eligible for the randomised trial if they report a pattern of binge drinking and score 15 or lower on the AUDIT (scores above 15 were referred to the Drug Abuse Programme for Treatment). Patients eligible for the study will be binge drinkers, defined as men who had drunk 5 or more standard drinks per occasion (12.8 g of alcohol per drink) on 1 or more occasions in the previous month. Women will be included in the study sample if they had drunk 4 or more standard drinks per occasion on 1 or more occasions in the previous month.
- •Rubio, G., Bermejo, J., Caballero, C., Santo-Domingo, J. Validación del test de identificación de trastornos por uso de alcohol (AUDIT) en atención primaria (Spanish validation of the Alcohol Use Disorders Identification Test [AUDIT] in primary care). Rev Clin Esp 1998; 198: 11-14.
Exclusion Criteria
- •1. Pregnant women
- •2. Plan to move out of the area within the year
- •3. Do not have a telephone
- •4. Those who are already participating in an alcohol intervention programme
- •5. Those who have an Axis I psychiatric disorder (American Psychiatric Association [APA] 2000) other than substance abuse that, in the judgment of the PCPh, prevents them from participating
- •6. Unable to complete the informed consent
Investigators
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