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CompletedNCT01544803Updated Mar 17, 2025

Randomized Controlled Trial of eScreen for Problematic Alcohol Use

A Phase 2 interventional study of eScreen and Alkoholhjalpen in Problematic AOD Use, sponsored by Karolinska Institutet. Completed at 1 site in Sweden. Open to participants aged 15 Years to 85 Years. Per ClinicalTrials.gov, last updated 2025-03-17.

Sponsored by Karolinska Institutet · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
633
Allocation
Randomized
Ages
15 Years to 85 Years
Sex
All
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Study summary

Objectives: This study compares the efficacy of eScreen and Alkoholhjalpen in a three-armed randomized controlled design, measuring outcomes in terms of changes in problematic alcohol use up to one year after study recruitment. The eScreen brief Internet intervention for problematic alcohol and drug use offers self-screening, in-depth self-reporting, personalized feedback and treatment recommendations as well as an electronic diary. Progress over time is shown in diagrams detailing consumption levels. A more extensive Internet intervention for problematic alcohol use, Alkoholhjalpen,provides CBT- and MI-based psycho-education with a solution-oriented focus, electronic diary and moderated chat-forum.

Method: Participants with problematic alcohol use (AUDIT >7 for men and >5 for women) are randomized into one of three groups: T1, eScreen referral (n=211); T2, Alkoholhjalpen referral (n=211); Control group (n=211). Outcomes on alcohol use as well as health-related symptoms are assessed after 3, 6 and 12 months.

The first hypothesis is that all three groups will reduce their alcohol consumption and alcohol-related problems at follow-ups compared to the baseline level. The second hypothesis is that there will be no differences between participants in the eScreen and the Alkoholhjalpen group in reduction of alcohol consumption and alcohol-related problems at follow-ups. The third hypothesis is that participants in the eScreen and the Alkoholhjalpen group will show a greater reduction in alcohol consumption and alcohol-related problems compared to the control group (no intervention) at follow-ups. For a greater understanding of the study results possible other interventions received by the study participants for their problematic alcohol use during these 12 months of study participation will be investigated.

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Conditions studied

  • Problematic AOD Use

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Keywords

  • Randomized Controlled Trial
  • Alcohol
  • Internet
  • Screening
  • Brief intervention
  • Personalized feedback
03

In context

Alcohol Drinking

925 studies on the registry are indexed under Alcohol Drinking; 172 are open to participants now.

This study's enrollment of 633 is above the median of 108 across 802 interventional studies indexed under Alcohol Drinking.

Browse Alcohol Drinking studies →

Lead sponsor

Karolinska Institutet is the lead sponsor of 1,113 studies on the registry; 267 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
15 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Problematic alcohol use. AUDIT>7 for men and AUDIT>5 for women

Exclusion criteria

Exclusion Criteria:

  • Drug use DUDIT>0
  • Unproblematic alcohol use, AUDIT\<8 for men and AUDIT\<6 for women
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Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Single (Investigator)
Enrollment
633 participants (actual)

Study arms

  • No intervention
    Control group
  • Experimental
    Web based self-monitoring

    Behavioral: eScreen

  • Active comparator
    Web based self-help

    Behavioral: Alkoholhjalpen

Interventions

  • BehavioraleScreen

    The eScreen brief Internet intervention for problematic alcohol and drug use offers self-screening, in-depth self-reporting, personalized feedback and treatment recommendations as well as an electronic diary. Progress over time is shown in diagrams detailing consumption levels.

    Also known as: www.escreen.se

  • BehavioralAlkoholhjalpen

    An extensive Internet intervention for problematic alcohol use, Alkoholhjalpen,provides CBT- and MI-based psycho-education with a solution-oriented focus, electronic diary and moderated chat-forum.

    Also known as: www.alkoholhjalpen.se

06

What researchers measure

Primary outcomes

  1. Change in the total AUDIT-C score

    The primary outcome measure for this trial was the change in the total AUDIT score for the first three AUDIT questions, as a measure of alcohol consumption only, referred to as the AUDIT-C.

    Time frame: 3, 6 and 12 months

Secondary outcomes

  1. AUDIT

    Change in total AUDIT score, as a summarized measure of alcohol use (including alcohol consumption and alcohol-related problems).

    Time frame: 3, 6 and 12 months

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Study locations

1 site
  • Karolinska Institutet, Department of Clinical Neuroscience
    Stockholm, 17176, Sweden
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References and documents

Publications

  • Sinadinovic K, Berman AH, Hasson D, Wennberg P. Internet-based assessment and self-monitoring of problematic alcohol and drug use. Addict Behav. 2010 May;35(5):464-70. doi: 10.1016/j.addbeh.2009.12.021. Epub 2010 Jan 4. Erratum In: Addict Behav. 2010 Sep;35(9):853. PubMed 20092953 ↗
  • Sinadinovic K, Wennberg P, Berman AH. Population screening of risky alcohol and drug use via Internet and Interactive Voice Response (IVR): a feasibility and psychometric study in a random sample. Drug Alcohol Depend. 2011 Mar 1;114(1):55-60. doi: 10.1016/j.drugalcdep.2010.09.004. Epub 2010 Oct 27. PubMed 21030164 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01544803
Lead sponsor
Karolinska Institutet
Responsible party
Anne H Berman (Associate Professor, Karolinska Institutet) — Principal investigator
First posted
Mar 6, 2012
Start date
Sep 2009
Primary completion
Oct 2010
Completion
Oct 2011
Last update
Mar 17, 2025

Study contacts

Anne H Berman, PhD
principal investigator · Karolinska Institutet

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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