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Clinical Trials/NCT01923246
NCT01923246CompletedNot Applicable

Development of IVR and WEB Alcohol Interventions

Region Skane2 sites in 1 country1,672 target enrollmentStarted: September 2011Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,672
Locations
2
Primary Endpoint
ALCOHOL USE DISORDERS IDENTIFICATION TEST (AUDIT)
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The primary aim of the present study is to study the effect of a brief automated alcohol intervention in University students, and if there is a difference in effect between automated brief interventions delivered by internet (WEB) or Interactive Voice Response (IVR), and to study if there is difference in effect between single and repeated interventions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Prevention
Masking
Single (Investigator)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Females scoring 6 and above and males scoring 8 and above on AUDIT.

Exclusion Criteria

  • •Females scoring 5 and below and males scoring 7 and below on AUDIT

Outcomes

Primary Outcomes

ALCOHOL USE DISORDERS IDENTIFICATION TEST (AUDIT)

Time Frame: September 2011 - October 2011

Secondary Outcomes

  • Daily Drinking Questionnaire (DDQ)(September 2011 - October 2011)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Claes Andersson

PhD

Region Skane

Study Sites (2)

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