Development of IVR and WEB Alcohol Interventions

August 13, 2013 updated by: Claes Andersson, Region Skane
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 Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

1672

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Sweden
    • Skane
      • Malmö, Skane, Sweden, 20506
        • Malmö university, Department of Criminology

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Single WEB intervention
Web intervention recieved once.
Behavioral: Single WEB intervention
Brief WEB intervention recieved once
Experimental: Repeated WEB intervention
Web intervention recieved twice.
Behavioral: Repeated WEB intervention
WEB intervention recieved twice.
Experimental: Single IVR intervention
IVR intervention recieved once
Behavioral: Single IVR intervention
IVR intervention recieved once
Experimental: Repeated IVR intervention
IVR intervention recieved twice
Behavioral: Repeated IVR intervention
IVR intervention recieved twice
No Intervention: Control group
Untreated Control Group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
ALCOHOL USE DISORDERS IDENTIFICATION TEST (AUDIT)
Time Frame: September 2011 - October 2011
September 2011 - October 2011

Secondary Outcome Measures

Outcome Measure
Time Frame
Daily Drinking Questionnaire (DDQ)
Time Frame: September 2011 - October 2011
September 2011 - October 2011

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Region Skane

Investigators

  • Principal Investigator: Claes Andersson, PhD, Malmö university, Department of Criminology

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2011

Primary Completion (Actual)

October 1, 2011

Study Completion (Actual)

October 1, 2011

Study Registration Dates

First Submitted

August 13, 2013

First Submitted That Met QC Criteria

August 13, 2013

First Posted (Estimate)

August 15, 2013

Study Record Updates

Last Update Posted (Estimate)

August 15, 2013

Last Update Submitted That Met QC Criteria

August 13, 2013

Last Verified

August 1, 2013

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • FHI 2006/100
  • 2006/100 (Other Grant/Funding Number: Swedish National Institute of Public Health)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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