Binge Drinking Clinical Trial
Official title:
Brief Alcohol Interventions With Mobile Phone Applications for University Students: Interventions Targeting Differing Risk Levels in Two Consecutive Randomized Controlled Trials
The purpose of this study is to evaluate the efficacy of three mobile phone applications,
Promillekoll, PartyPlanner and TeleCoach among university student union members with
problematic drinking. Two trials are conducted, one a three-armed randomized controlled
study, and the second a two-armed randomized control study. Outcomes are measured in terms
of changes in problematic alcohol use at follow up 6,12 and 18 weeks after baseline data
gathering. Both the Promillekoll and PartyPlanner apps feature real time registration of
alcohol consumption and give feedback of estimated blood alcohol concentration levels.
PartyPlanner also allows for planning an alcohol consumption event in advance and for later
comparison of the plan with actual consumption. Study 1 compares these two apps with a
control group. In Study 2, participants reporting alcohol consumption above the weekly
recommended level are redirected to randomized assignment to an in-depth app, TeleCoach,
which offers different exercises for reducing alcohol use. After 6 weeks the controls are
offered the TeleCoach intervention for 6 weeks, and the first intervention group loses app
access. In both studies, followup occurs 6, 12 and 18 weeks after baseline registration.
Hypotheses:
Study 1: 1. The groups receiving the Promillekoll and PartyPlanner interventions will reduce
their alcohol use to a larger extent than the control group at follow-up compared to the
baseline level. 2. The planning function in PartyPlanner will be associated with an
increased decrease in alcohol consumption compared to only real-time use for Promillekoll.
Study 2: The proportion of participants with risky use above recommended levels will decline
faster in the group that receives the intervention first, in comparison to controls.
Status | Completed |
Enrollment | 2166 |
Est. completion date | March 2015 |
Est. primary completion date | March 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - membership in the included student unions Exclusion Criteria: |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Sweden | Karolinska institutet, Department of Clinical Neuroscience | Stockholm |
Lead Sponsor | Collaborator |
---|---|
Karolinska Institutet |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in estimated Blood Alcohol Concentration (eBAC) | Change in Blood Alcohol Concentration estimated using Widmark's formula for Blood Alcohol Concentration estimation. | 6, 12 and 18 weeks | No |
Primary | Alcohol Use Disorders Identification Test (AUDIT) | Change in total AUDIT score, as a summarized measure of alcohol use (including alcohol consumption and alcohol-related problems). | 6, 12 and 18 weeks | No |
Secondary | Quantity | Number of standard drinks consumed over a typical week during last month. | 6, 12 and 18 weeks | No |
Secondary | Frequency | Number of drinking occasions over a typical week during the last month | 6, 12 and 18 weeks | No |
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