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Clinical Trials/NCT00278733
NCT00278733
Completed
Not Applicable

Campus Health Intervention Projects to Reduce High Risk Drinking Among University Students by Means of Brief Physician Advice

University of British Columbia1 site in 1 country150 target enrollmentFebruary 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
High Risk Drinking
Sponsor
University of British Columbia
Enrollment
150
Locations
1
Primary Endpoint
A reduction in alcohol use and in the frequency of high risk drinking and related harms, measured at 6, 12, 18 and 24 months post intervention.
Status
Completed
Last Updated
19 years ago

Overview

Brief Summary

The goal of the study is to test the efficacy of brief physician advice in reducing the frequency of high risk drinking and alcohol-related harm in a population of university students seeking routine care at UBC Student Health Service. It is hypothesized that receiving the intervention will reduce the amount of alcohol consumed and the incidence of alcohol-related harm among the students in the intervention group, as compared to the control group.

Detailed Description

We estimate that roughly 3000 students will need to be screened to obtain sufficient eligible participants to randomize 150 students. High-risk drinkers will be identified by means of an embedded alcohol screening survey, which will be distributed through Student Health Services. Those deemed eligible through the screening survey and who have agreed to be contacted will be invited to attend a baseline interview, which will further define eligibility and assign interested students to the control or intervention group. Those randomized to the usual care control group will receive a self-help health booklet and will be contacted to complete a follow-up telephone interview at 6, 12, 18 and 24 months. Those randomized to the intervention group will receive the same booklet and will meet with a Student Health Service physician. There will be two face-to-face meetings with the physician and two follow up phone calls by the physician. The physicians use a scripted workbook, diary cards and other materials designed to reduce alcohol use and the frequency of high risk drinking. Those in the intervention group will also be contacted to complete a follow-up telephone interview at 6, 12, 18 and 24 months. Outcome data will also be sought, with participants' permission, from campus organizations including Campus Housing, Security, the RCMP and the Registrar.

Registry
clinicaltrials.gov
Start Date
February 2006
End Date
May 2008
Last Updated
19 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Full time students 18 and older; students seeking routine care at UBC Student Health Services; students who report high risk drinking in the last 28 days; students able to read and communicate in English

Exclusion Criteria

  • Students graduating or leaving campus before the first intervention is complete; students who are acutely ill; students who are under 18 years; female students who are pregnant; students who are suicidal; students consuming more than 200 drinks in the past 28 days

Outcomes

Primary Outcomes

A reduction in alcohol use and in the frequency of high risk drinking and related harms, measured at 6, 12, 18 and 24 months post intervention.

Secondary Outcomes

  • Academic performance; contact with Campus Security or RCMP; incidents reported by campus housing; hospitalizations for injury or accident, as measured at 6, 12 18 and 24 months post intervention.

Study Sites (1)

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