World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ISRCTN
Last refreshed on: 8 June 2020
Main ID:  ISRCTN52150713
Date of registration: 02/06/2017
Prospective Registration: Yes
Primary sponsor: Swiss Reseach Institute for Public Health and Addiction
Public title: Just-in-time delivered planning intervention to reduce alcohol use in adolescents
Scientific title: Efficacy of a just-in-time delivered planning intervention to reduce alcohol use in adolescents with hazardous alcohol consumption: a micro-randomized controlled trial
Date of first enrolment: 22/06/2017
Target sample size: 79
Recruitment status: Completed
URL:  http://isrctn.com/ISRCTN52150713
Study type:  Interventional
Study design:  Micro-randomized controlled trial (Prevention)  
Phase:  Not Applicable
Countries of recruitment
Switzerland
Contacts
Name: Severin    Haug
Address:  Konradstrasse 32 8031 Zurich Switzerland
Telephone: +41 (0)44 448 11 74
Email: severin.haug@isgf.uzh.ch
Affiliation: 
Name:    
Address: 
Telephone:
Email:
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria:
1. Ownership of a mobile phone
2. Hazardous alcohol use defined by binge drinking: consumption of 5 (male; female: 4) or more alcoholic standard drinks on one or more occasions within 30 days preceding the baseline assessment
3. Aged 16 or over

Exclusion criteria:
1. No alcohol consumption with friends or when going out in the evening
2. Typical drinking time with friends or when going out: in the morning or afternoon
3. Age < 16


Age minimum:
Age maximum:
Gender: Both
Health Condition(s) or Problem(s) studied
Alcohol prevention
Mental and Behavioural Disorders
Mental and behavioural disorders due to use of alcohol
Intervention(s)

Participants receive the just-in-time delivered planning intervention to reduce alcohol use on their typically indicated drinking day at 5pm. The study has an AB/BA crossover design, in which each participant receives the intervention and the control in a randomized order. The randomization sequence will be created using computerized random numbers. There is a period of at least 2 weeks between the intervention and control.

Intervention points in time include:
1. Assessment of state of receptivity and state of vulnerability via SMS text message question (“Are you planning to go out or meet with friend this evening?”) on the typical individually indicated drinking day at 5pm
2. Confirmation of receptivity and vulnerability by a text message reply (“Yes”) from the participant
3. The digital micro intervention where participants can choose one of two predetermined if-then plans to practice sensible drinking via SMS text messaging and another text message prompt to visualize the chosen plan

Control points in time only include 1 and 2.

Follow-up assessments will be conducted 24 hours after the assessment of state of receptivity and vulnerability in both intervention and control points in time.
Primary Outcome(s)

Number of alcoholic standard drinks consumed during the previous evening/night, measured via an SMS text message "How many alcoholic drinks did you have last evening/night?” at 24 hours after the assessment of state of receptivity and vulnerability (i.e., at 5pm the following day)
Secondary Outcome(s)
Binge drinking: consumption of 5 (male) or 4 (female) or more alcoholic standard drinks during the previous evening/night, measured via an SMS text message "How many alcoholic drinks did you have last evening/night?” at 24 hours after the assessment of state of receptivity and vulnerability (i.e., at 5pm the following day)
Secondary ID(s)
17.4.11
Source(s) of Monetary Support
Swiss Research Institute for Public Health and Addiction, Swiss Federal Office of Public Health
Secondary Sponsor(s)
Ethics review
Status:
Approval date:
Contact:
Ethics committee of the Faculty of Philosophy at the University of Zurich, 18/04/2017, ref: 17.4.11
Results
Results available: Yes
Date Posted:
Date Completed: 31/12/2018
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history