Binge DrinkingNCT02064998
Two Consecutive Randomized Controlled Trials Using Mobile Phone Applications for Risky Alcohol Use
A study testing Promillekoll, PartyPlanner and TeleCoach in people with Binge Drinking and Problematic AOD Use, run by Karolinska Institutet at 1 site in Sweden.
Trial 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. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Binge Drinking, Problematic AOD Use
- What is being tested?
- Promillekoll, PartyPlanner and TeleCoach
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 2,166 participants
- Where
- 1 siteSweden
- Study dates
- Sep 2014to Mar 2015
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- membership in the included student unions
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
Sweden1 site
Karolinska institutet, Department of Clinical Neuroscience
Stockholm, 11364
About this study
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:
Read more
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.
Read the 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.
- Conditions
- Binge Drinking, Problematic AOD Use
- Being tested
- Promillekoll, PartyPlanner, TeleCoach
- Keywords
- Randomized Controlled Trial, Alcohol, Internet, Mobile phone, Screening, Brief intervention
- Medical subject headings
- Binge Drinking
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PromillekollBehavioural
Smartphone app monitoring alcohol use with feedback on eBAC level.
PartyPlannerBehavioural
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.
TeleCoachBehavioural
Smartphone app providing exercises and vignettes for reducing or abstaining from alcohol consumption.
| Study group | Role | What they receive |
|---|---|---|
| Promillekoll | Experimental | Smartphone app monitoring alcohol use with feedback on eBAC level. Receives: Behavioral: Promillekoll |
| PartyPlanner | Experimental | 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. Receives: Behavioral: PartyPlanner |
| Control Study 1 | No intervention | Waitlist control group that is given access to the Promillekoll and PartyPlanner apps after a 12-week wait. |
| Crossover group 1: TeleCoach - Control | Experimental | 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. Receives: Behavioral: TeleCoach |
| Crossover group 2: Control - TeleCoach | Experimental | 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. Receives: Behavioral: TeleCoach |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in estimated Blood Alcohol Concentration (eBAC)
Change in Blood Alcohol Concentration estimated using Widmark's formula for Blood Alcohol Concentration estimation.
Measured: 6, 12 and 18 weeks
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).
Measured: 6, 12 and 18 weeks
Secondary outcomes (2)
Quantity
Number of standard drinks consumed over a typical week during last month.
Measured: 6, 12 and 18 weeks
Frequency
Number of drinking occasions over a typical week during the last month
Measured: 6, 12 and 18 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Feb 2014 (estimated)
- Study startSep 2014
- Primary completionMar 2015
- Study completionMar 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Binge DrinkingStudies of the same condition, open and under way.
- More trials run by Karolinska InstitutetThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 2,166 participants (actual)
Sponsor and investigators
- Lead sponsor
- Karolinska Institutet
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Anne H Berman, Karolinska Institutet
- Investigators
- Anne H Berman, PhD, Principal investigator, Karolinska Institutet
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02064998
- Sponsor's protocol ID
- 2014/278-31/2
- Other IDs
- KI 2-2439/2014 (PuL)
- Status last verified
- Aug 2015
- First submitted
- 14 Feb 2014
- Last updated
- 1 Sep 2015
- Results posted
- No
- Data monitoring committee
- No
Publications
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.
PubMed 28224445Berman 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.
PubMed 26693967
Study at a glance
From the registry record, last updated by the sponsor on 1 Sep 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Brief Alcohol Interventions With Mobile Phone Applications for University Students: Interventions Targeting Differing Risk Levels in Two Consecutive Randomized Controlled Trials
- ClinicalTrials.gov ID
- NCT02064998
- Acronym / sponsor ID
- 2014/278-31/2
- Conditions
- Binge Drinking, Problematic AOD Use
- Keywords
- Randomized Controlled Trial, Alcohol, Internet, Mobile phone, Screening, Brief intervention
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 2,166 participants (actual)
- Lead sponsor
- Karolinska InstitutetUniversity, hospital or other
- Study start
- Sep 2014
- Primary completion
- Mar 2015 (actual)
- Study completion
- Mar 2015 (actual)
- First posted
- 17 Feb 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 5
| Arm | Type | Receives |
|---|---|---|
| Promillekoll | Experimental | Behavioral: PromillekollSmartphone app monitoring alcohol use with feedback on eBAC level. |
| PartyPlanner | Experimental | Behavioral: PartyPlannerSmartphone-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. |
| Control Study 1 | No intervention | –Waitlist control group that is given access to the Promillekoll and PartyPlanner apps after a 12-week wait. |
| Crossover group 1: TeleCoach - Control | Experimental | Behavioral: TeleCoachSix-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. |
| Crossover group 2: Control - TeleCoach | Experimental | Behavioral: TeleCoachInitially 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. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- membership in the included student unions
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PromillekollSmartphone app monitoring alcohol use with feedback on eBAC level. | Behavioural | Promillekoll |
| PartyPlannerSmartphone-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. | Behavioural | PartyPlanner |
| TeleCoachSmartphone app providing exercises and vignettes for reducing or abstaining from alcohol consumption. | Behavioural | Crossover group 1: TeleCoach - Control, Crossover group 2: Control - TeleCoach |
Primary outcome
Change in estimated Blood Alcohol Concentration (eBAC)
Time frame: 6, 12 and 18 weeks
Change in Blood Alcohol Concentration estimated using Widmark's formula for Blood Alcohol Concentration estimation.
Alcohol Use Disorders Identification Test (AUDIT)
Time frame: 6, 12 and 18 weeks
Change in total AUDIT score, as a summarized measure of alcohol use (including alcohol consumption and alcohol-related problems).
2 secondary outcomes
Quantity
Time frame: 6, 12 and 18 weeks
Frequency
Time frame: 6, 12 and 18 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Sep 2015.
- Derived from this study: PubMed 28224445Gajecki 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.
- Derived from this study: PubMed 26693967Berman 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Anne H Berman, PhD principal investigator
Karolinska Institutet
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Promillekoll, PartyPlanner and TeleCoach in people with Binge Drinking and Problematic AOD Use, run by Karolinska Institutet at 1 site in Sweden.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Sep 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in estimated Blood Alcohol Concentration (eBAC) (time frame: 6, 12 and 18 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02064998, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Sep 2015.