Back to resultsDevelopment of IVR and WEB Alcohol Interventions
Primary Purpose
Alcohol Consumption
Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Single WEB intervention
Repeated WEB intervention
Single IVR intervention
Repeated IVR intervention
Sponsored by
About this trial
This is an interventional prevention trial for Alcohol Consumption focused on measuring Alcohol consumption, Brief intervention, Automated techniques
Eligibility Criteria
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
Sites / Locations
- Malmö university, Department of Criminology
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Experimental
Experimental
Experimental
Experimental
No Intervention
Arm Label
Single WEB intervention
Repeated WEB intervention
Single IVR intervention
Repeated IVR intervention
Control group
Arm Description
Web intervention recieved once.
Web intervention recieved twice.
IVR intervention recieved once
IVR intervention recieved twice
Untreated Control Group.
Outcomes
Primary Outcome Measures
ALCOHOL USE DISORDERS IDENTIFICATION TEST (AUDIT)
Secondary Outcome Measures
Daily Drinking Questionnaire (DDQ)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01923246
Brief Title
Development of IVR and WEB Alcohol Interventions
Official Title
Development of IVR and WEB Alcohol Interventions
Study Type
Interventional
2. Study Status
Record Verification Date
August 2013
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
October 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Region Skane
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Consumption
Keywords
Alcohol consumption, Brief intervention, Automated techniques
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
1672 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single WEB intervention
Arm Type
Experimental
Arm Description
Web intervention recieved once.
Arm Title
Repeated WEB intervention
Arm Type
Experimental
Arm Description
Web intervention recieved twice.
Arm Title
Single IVR intervention
Arm Type
Experimental
Arm Description
IVR intervention recieved once
Arm Title
Repeated IVR intervention
Arm Type
Experimental
Arm Description
IVR intervention recieved twice
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Untreated Control Group.
Intervention Type
Behavioral
Intervention Name(s)
Single WEB intervention
Intervention Description
Brief WEB intervention recieved once
Intervention Type
Behavioral
Intervention Name(s)
Repeated WEB intervention
Intervention Description
WEB intervention recieved twice.
Intervention Type
Behavioral
Intervention Name(s)
Single IVR intervention
Intervention Description
IVR intervention recieved once
Intervention Type
Behavioral
Intervention Name(s)
Repeated IVR intervention
Intervention Description
IVR intervention recieved twice
Primary Outcome Measure Information:
Title
ALCOHOL USE DISORDERS IDENTIFICATION TEST (AUDIT)
Time Frame
September 2011 - October 2011
Secondary Outcome Measure Information:
Title
Daily Drinking Questionnaire (DDQ)
Time Frame
September 2011 - October 2011
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claes Andersson, PhD
Organizational Affiliation
Malmö University, Department of Criminology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Malmö university, Department of Criminology
City
Malmö
State/Province
Skane
ZIP/Postal Code
20506
Country
Sweden
12. IPD Sharing Statement
Learn more about this trial
Development of IVR and WEB Alcohol Interventions
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