Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06789250

Co-occurence of Mental Illness and Problematic Alcohol Use: an Internet-based Cognitive Behavior Therapy Intervention

Led by Linkoeping University · Updated on 2025-02-24

240

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating internet-based cognitive behavior therapy (ICBT) to treat adults with co-occurring problematic alcohol use and mild to moderate symptoms of mental illness, such as depression, anxiety, stress, or sleep disturbances. The study aims to find out if the ICBT program can reduce self-reported mental health suffering and alcohol intake compared to a control group receiving weekly attention from the research team. Participants will receive either 10 weeks of individually tailored, therapist-supported ICBT modules delivered on their computer or be placed in a wait-list control group that receives weekly attention but no immediate treatment. After the initial 10 weeks and post-treatment assessments, the control group will also have the opportunity to complete the same ICBT program. Therapists provide both scheduled weekly and on-demand support during weekdays. During the study, participants will complete forms rating their mental health and alcohol use at the start, weekly during treatment, at the end of treatment, and at 6 and 12 months follow-up via online surveys. Researchers will measure changes in depression, anxiety, and stress symptoms using the DASS-21 scale and track alcohol intake through self-reports. Additional assessments will include insomnia symptoms, disability, craving, and other mental health and alcohol-related measures. The total study duration includes treatment and follow-up over 12 months after treatment ends.

CONDITIONS

Brief Title

Co-occurence of Mental Illness and Problematic Alcohol Use: an Internet-based Cognitive Behavior Therapy Intervention

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • AUDIT score of 6 or higher for women, 8 or higher for men
  • Symptoms of depression, anxiety disorder, or stress-related illness
  • Ability to speak, read, and write Swedish adequately
  • Access to the internet and a smartphone, computer, or other device
Not Eligible

You will not qualify if you...

  • Currently receiving psychological treatment
  • Currently using medication for alcohol use disorder
  • Recent changes in psychiatric medication within the past three months or planned changes during treatment
  • Severe psychiatric disorders based on MINI interview and medical history
  • Severe medical conditions that could affect participation
  • Severe cognitive impairment
  • Current suicidality
  • Severe alcohol addiction requiring specialized treatment
  • Risk of severe alcohol withdrawal needing medical treatment unless completed withdrawal treatment
  • Substance use disorder other than alcohol or nicotine within the past six months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) to assess eligibility criteria

Outpatient Treatment

Duration - 10 weeks

Participants undergo 10 weeks of therapist-supported, individually tailored, internet-based cognitive behavior therapy targeting harmful alcohol use and co-occurring psychological symptoms.

Weekly online sessions with therapist support and on-demand assistance

Follow-up

Duration - 12 months

Participants are monitored for 12 months after the end of treatment to assess changes in alcohol use and psychological symptoms.

Follow-up assessments at 3 months (end of treatment), 6 months, and 12 months after treatment

Trial Site Locations

Total: 2 locations

1

Linköping University

Linköping, Sweden, 58183

Actively Recruiting

2

Department of Behavioral Sciences and Learning, Linköping University

Linköping, Östergötland County, Sweden, 58183

Not Yet Recruiting

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Research Team

G

Gerhard Andersson, Professor

Å

Åsa Steensland, PhD student

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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