- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06018389
Prevention of Hazardous Use of Alcohol with Danish High School Students (Our Choice)
Prevention of Hazardous Use of Alcohol Among High School Students in Denmark: a Cluster Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The main aim of the 'Our Choice' cluster randomized controlled multisite trial is to test the efficacy of interventions aimed at reducing hazardous use of alcohol and related health outcomes among first-year students (15-18 years) in high schools in Denmark. Furthermore, the aim is to examine feasibility and acceptability of the interventions with Danish students in high school, as well as with staff (e.g., teachers and principals) to inform future implementation studies.
The study employs a parallel group cluster randomized controlled trial design with three conditions:
- Structural condition targeting school and parent levels via school policies for school-based social events and an information-based interactive parent meeting.
- Structural condition combined with group-based Motivational Interviewing (group MI) which also targets the student level.
- Assessment-only control condition with the same assessments as the other two conditions and with interventions offered after the last follow-up survey.
The study hypothesizes that students in the structural condition (school and parent levels) reduce hazardous alcohol use and related health outcomes compared to students in the assessment-only control condition 12 months post baseline; and that adding group MI yields further improvements.
A participatory approach is used to adapt and develop interventions. Sixteen high schools in Denmark and N=3100 first-year students enrolled in high school in August 2023 will be recruited. Data will be collected via online questionnaires pre-interventions (baseline), 2, 6, 9 and 12 months post baseline. The primary outcome will be analyzed with generalized linear mixed models. Feasibility and acceptability will be assessed via surveys (students) and interviews (high school staff) to inform future implementation.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Aarhus, Denmark
- Centre for Alcohol and Drug Research, Aarhus BSS, Aarhus University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Students starting high school in one of the 16 participating high schools in August 2023
- Minimum 15 years old
- Understand and speak Danish
- Able to give independent informed consent
- Staff (school principals, teachers, or administrative employees) from one of the 16 participating high schools
Exclusion Criteria:
- Under 15 years old
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Structural Only
The Structural Only condition consists of (1) school policies for school-based social events; and (2) an information-based interactive parent meeting.
Interventions in this arm are targeting the school and parent level.
|
A shared list of school policies for or related to, school-based social events at school premises. The policy initiatives include (but are not limited to): increasing the number of social events without alcohol; promoting non-alcoholic beverages at parties; working with student associations regarding their roles and responsibilities; encouraging parental involvement at school events and disseminating the schools' alcohol policy among students and parents. The school principal and management will be responsible for the implementation and enforcement of the policies. The Information-based interactive parent meetings will be 45 minutes and will take place at the schools. Parents will be offered concrete, research-informed advice about how they can reduce risk of hazardous substance use and promote well-being among their adolescents. Following a 15-minute presentation, the group leader facilitates a discussion and exchange of experience between parents. |
|
Experimental: Structural+Group MI
The Structural+Group MI condition consists of the elements described in "Structural Only" and group MI.
Interventions in this arm are targeting all three levels: school, parent and student level.
|
A shared list of school policies for or related to, school-based social events at school premises. The policy initiatives include (but are not limited to): increasing the number of social events without alcohol; promoting non-alcoholic beverages at parties; working with student associations regarding their roles and responsibilities; encouraging parental involvement at school events and disseminating the schools' alcohol policy among students and parents. The school principal and management will be responsible for the implementation and enforcement of the policies. The Information-based interactive parent meetings will be 45 minutes and will take place at the schools. Parents will be offered concrete, research-informed advice about how they can reduce risk of hazardous substance use and promote well-being among their adolescents. Following a 15-minute presentation, the group leader facilitates a discussion and exchange of experience between parents.
Within school classes, students are divided into groups of 5-8 students and each group will be assigned a group leader from the research team.
The group-based Motivational Interviewing (group MI) is manualized and consists of two one-hour group sessions administered over two consecutive weeks.
The first session is focused on "Tell your story", "Gains from not drinking", and "Social norms."
In the second session, the focus is on "Personal values", "Linking values with behavior" and "Planning/choices regarding alcohol".
Both group MI sessions will take place at the schools during the school day.
|
|
No Intervention: Control
The Control condition is an assessment-only condition.
During the period under study, it includes the same assessments (surveys) as the other two conditions.
After the last follow-up (August 2024), control schools can opt-in to receive any of the intervention programs.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Past month high-intensity drinking
Time Frame: From baseline to 12 months after baseline
|
Past month high-intensity drinking: peak drinks per drinking event, assessed with the Timeline FollowBack (TLFB) (count measure)
|
From baseline to 12 months after baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Past month heavy episodic drinking events
Time Frame: From baseline to 12 months after baseline
|
Past month heavy episodic drinking events assessed by TLFB (count measure).
|
From baseline to 12 months after baseline
|
|
Past month alcohol-related consequences
Time Frame: From baseline to 12 months after baseline
|
Assessed by 21 items covering physical, social and mental issues related to hazardous use of alcohol, developed by the team for Danish youth based on single items from previous Danish surveys and the Rutgers Alcohol Problems Index e.g.
black-outs, (emotional) hangovers), sexual contact that was later regretted, with yes/no response options (summed score: range 0-21) with higher scores indicating more negative consequences.
|
From baseline to 12 months after baseline
|
|
Well-being in class
Time Frame: From baseline to 12 months after baseline
|
Assessed by six items rated on a five-point scale from 'completely disagree' to 'completely agree' e.g., I feel accepted by the others in my class (summed score: range 0-30) with a score of 30 representing the best possible well-being in class.
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From baseline to 12 months after baseline
|
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World Health Organization Five Well-being Index (WHO-5)
Time Frame: From baseline to 12 months after baseline
|
Psychological well-being, assessed by The World Health Organization Five Well-being Index (summed score: range 0-25) with a score of 25 representing the best possible quality of life.
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From baseline to 12 months after baseline
|
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Past month use of tobacco
Time Frame: From baseline to 12 months after baseline
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Measured by days using tobacco (count measure: range 0-30 days)
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From baseline to 12 months after baseline
|
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Past month use of illegal substances
Time Frame: From baseline to 12 months after baseline
|
Measured by days using cannabis, cocaine, and other illegal drugs (count measure: range 0-30 days).
|
From baseline to 12 months after baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Krisrtine Rømer Thomsen, Centre for Alcohol and Drug Research, Aarhus BSS, Aarhus University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- voresvalg_40833
- 2022-0367531 seqno. 3073 (Other Identifier: AU record, University of Aarhus)
- ID: 155933 (Other Identifier: TrygFonden)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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