search
Back to results

Two Consecutive Randomized Controlled Trials Using Mobile Phone Applications for Risky Alcohol Use

Primary Purpose

Binge Drinking, Problematic AOD Use

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Promillekoll
PartyPlanner
TeleCoach
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Binge Drinking focused on measuring Randomized Controlled Trial, Alcohol, Internet, Mobile phone, Screening, Brief intervention

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • membership in the included student unions

Exclusion Criteria:

Sites / Locations

  • Karolinska institutet, Department of Clinical Neuroscience

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Experimental

Experimental

No Intervention

Experimental

Experimental

Arm Label

Promillekoll

PartyPlanner

Control Study 1

Crossover group 1: TeleCoach - Control

Crossover group 2: Control - TeleCoach

Arm Description

Smartphone app monitoring alcohol use with feedback on eBAC level.

Smartphone-adapted web-based app for simulating an event with alcohol consumption in advance, real time monitoring of alcohol use with eBAC feedback during the event and later possibility of comparison between the plan and the event.

Waitlist control group that is given access to the Promillekoll and PartyPlanner apps after a 12-week wait.

Six-week access to the TeleCoach app, with exercises and vignettes for reducing or abstaining from alcohol consumption, followed by a 6-week period with no access to the app.

Initially a 6 week no-app control period, followed by 6-week access to the TeleCoach app, offering exercises and vignettes for reducing or abstaining from alcohol consumption.

Outcomes

Primary Outcome Measures

Change in estimated Blood Alcohol Concentration (eBAC)
Change in Blood Alcohol Concentration estimated using Widmark's formula for Blood Alcohol Concentration estimation.
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).

Secondary Outcome Measures

Quantity
Number of standard drinks consumed over a typical week during last month.
Frequency
Number of drinking occasions over a typical week during the last month

Full Information

First Posted
February 14, 2014
Last Updated
August 31, 2015
Sponsor
Karolinska Institutet
search

1. Study Identification

Unique Protocol Identification Number
NCT02064998
Brief Title
Two Consecutive Randomized Controlled Trials Using Mobile Phone Applications for Risky Alcohol Use
Official Title
Brief Alcohol Interventions With Mobile Phone Applications for University Students: Interventions Targeting Differing Risk Levels in Two Consecutive Randomized Controlled Trials
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
Objectives: This is a composite study consisting of Study 1 and Study 2: Study 1 evaluates the efficacy of two mobile phone applications, Promillekoll and PartyPlanner among university student union members at two or more universities in Sweden. The design is a three-armed randomized controlled trial, and outcomes are measured in terms of changes in problematic alcohol use at followup 6,12 and 18 weeks after baseline data collection. Both Promillekoll and PartyPlanner apps feature real time registration of alcohol consumption and feedback of estimated blood alcohol concentration (eBAC) levels. Both apps show the user when the estimated alcohol level is above 0.6%, a level that can lead to negative health consequences. PartyPlanner additionally provides the possibility of simulating and planning an alcohol consumption event in advance and later on comparing it with consumption at the actual event. Study 2: At the 6 week followup participants reporting an alcohol consumption above the weekly recommended level in Sweden will be redirected into Study 2. They will be asked to stop using any prior app for alcohol use. Half the group will be randomized to the TeleCoach app intervention, which offers the user different exercises for reducing or abstaining from alcohol use, depending on the user's goal (reduction or abstinence). This group will have access to the app for 6 weeks. The other half of the participants will be randomized to a waitlist control group for 6 weeks. Six weeks into the study, the TeleCoach intervention group will lose access to the app, and the waitlist control group will be given access to the TeleCoach app for 6 weeks. All participants (in both Study 1 and Study 2) will be followed up at 6, 12 and 18 weeks from initial baseline recruitment. Method: Study 1:Participants with problematic alcohol use (AUDIT >7 for men and >5 for women), having access to a smartphone running either the Android or the iOs operating systems, are randomized into one of three groups: 1. Access to Promillekoll, 2. Access to PartyPlanner and 3. Waitlist control group (gains access to both apps week 12). Alcohol use outcomes are collected 6,12 and 18 weeks after recruitment to the study. Study 2: At week 6 of Study 1, participants with risky weekly consumption, i.e. over 9 and 14 Swedish standard glasses (Swedish standard glass = 12 g of alcohol) for women and men respectively are randomized into one of two groups: 1. Access to TeleCoach for 6 weeks, followed by 6 weeks without the app. 2. Six weeks as waitlist controls followed by 6 weeks of access to TeleCoach. Alcohol use outcomes are collected 6 and 12 weeks after entering Study 2 (equivalent to 12 and 18 weeks after initial recruitment to Study 1). Students without problematic drinking and/or appropriate smartphones also participate in followups, in order to control for the regression to the mean phenomenon. All students who complete all baseline and followup questionnaires participate in a lottery with the chance of winning one of three computer tablets. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Binge Drinking, Problematic AOD Use
Keywords
Randomized Controlled Trial, Alcohol, Internet, Mobile phone, Screening, Brief intervention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
2166 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Promillekoll
Arm Type
Experimental
Arm Description
Smartphone app monitoring alcohol use with feedback on eBAC level.
Arm Title
PartyPlanner
Arm Type
Experimental
Arm Description
Smartphone-adapted web-based app for simulating an event with alcohol consumption in advance, real time monitoring of alcohol use with eBAC feedback during the event and later possibility of comparison between the plan and the event.
Arm Title
Control Study 1
Arm Type
No Intervention
Arm Description
Waitlist control group that is given access to the Promillekoll and PartyPlanner apps after a 12-week wait.
Arm Title
Crossover group 1: TeleCoach - Control
Arm Type
Experimental
Arm Description
Six-week access to the TeleCoach app, with exercises and vignettes for reducing or abstaining from alcohol consumption, followed by a 6-week period with no access to the app.
Arm Title
Crossover group 2: Control - TeleCoach
Arm Type
Experimental
Arm Description
Initially a 6 week no-app control period, followed by 6-week access to the TeleCoach app, offering exercises and vignettes for reducing or abstaining from alcohol consumption.
Intervention Type
Behavioral
Intervention Name(s)
Promillekoll
Intervention Description
Smartphone app monitoring alcohol use with feedback on eBAC level.
Intervention Type
Behavioral
Intervention Name(s)
PartyPlanner
Intervention Description
Smartphone-adapted web-based app for simulating an event with alcohol consumption in advance, real time monitoring of alcohol use with eBAC feedback during the event and later possibility of comparison between the plan and the event.
Intervention Type
Behavioral
Intervention Name(s)
TeleCoach
Intervention Description
Smartphone app providing exercises and vignettes for reducing or abstaining from alcohol consumption.
Primary Outcome Measure Information:
Title
Change in estimated Blood Alcohol Concentration (eBAC)
Description
Change in Blood Alcohol Concentration estimated using Widmark's formula for Blood Alcohol Concentration estimation.
Time Frame
6, 12 and 18 weeks
Title
Alcohol Use Disorders Identification Test (AUDIT)
Description
Change in total AUDIT score, as a summarized measure of alcohol use (including alcohol consumption and alcohol-related problems).
Time Frame
6, 12 and 18 weeks
Secondary Outcome Measure Information:
Title
Quantity
Description
Number of standard drinks consumed over a typical week during last month.
Time Frame
6, 12 and 18 weeks
Title
Frequency
Description
Number of drinking occasions over a typical week during the last month
Time Frame
6, 12 and 18 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: membership in the included student unions Exclusion Criteria:
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne H Berman, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska institutet, Department of Clinical Neuroscience
City
Stockholm
ZIP/Postal Code
11364
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
28224445
Citation
Gajecki M, Andersson C, Rosendahl I, Sinadinovic K, Fredriksson M, Berman AH. Skills Training via Smartphone App for University Students with Excessive Alcohol Consumption: a Randomized Controlled Trial. Int J Behav Med. 2017 Oct;24(5):778-788. doi: 10.1007/s12529-016-9629-9.
Results Reference
derived
PubMed Identifier
26693967
Citation
Berman AH, Gajecki M, Fredriksson M, Sinadinovic K, Andersson C. Mobile Phone Apps for University Students With Hazardous Alcohol Use: Study Protocol for Two Consecutive Randomized Controlled Trials. JMIR Res Protoc. 2015 Dec 22;4(4):e139. doi: 10.2196/resprot.4894.
Results Reference
derived
Links:
URL
http://ki.se/people/anberm
Description
Anne H Berman's research group profile

Learn more about this trial

Two Consecutive Randomized Controlled Trials Using Mobile Phone Applications for Risky Alcohol Use

We'll reach out to this number within 24 hrs