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OpenTrials
Completed

NCT Number: NCT01923246

Development of IVR and WEB Alcohol Interventions

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Malmö university, Department of Criminology

Malmö, Skåne County, 20506, Sweden

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Single WEB intervention

Behavioral

Brief WEB intervention recieved once

Repeated WEB intervention

Behavioral

WEB intervention recieved twice.

Single IVR intervention

Behavioral

IVR intervention recieved once

Repeated IVR intervention

Behavioral

IVR intervention recieved twice

Primary outcomes

  1. ALCOHOL USE DISORDERS IDENTIFICATION TEST (AUDIT)

    Time frame: September 2011 - October 2011

Secondary outcomes

  1. Daily Drinking Questionnaire (DDQ)

    Time frame: September 2011 - October 2011

Sponsors and collaborators

Lead sponsor

Region Skane

Other

Registry information

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Aug 15, 2013
Registry last updated
Aug 15, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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