ICBT for Mental Health Problems Related to the Coronavirus Pandemic

  • STATUS
    Recruiting
  • participants needed
    120
  • sponsor
    Linkoeping University
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Updated on 5 August 2020
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Summary

The study seeks to investigate the effects of a guided internet-based cognitive behavioral therapy (ICBT) programme a on adult mental health problems related to the current coronavirus pandemic. ICBT will be compared to a wait-list control group.

Participants will be recruited in Sweden with a nationwide recruitment.

Description

The study is set up as a randomized controlled trial. Quality of life, depressive symptoms, anxiety, sleep problems and traumatic stress will be measured. Given uncertainties regarding the psychological effects of Covid-19 pandemic a transproblematic tailored treatment approach will be used that has been tested in several previous trials. However, the present program has been adapted for the target population of people who are affected by the societal and individual consequences of the pandemic. The study does not focus on people who have or have had the corona virus.

Details
Condition Depression and Quality of Life Related to the Coronavirus Pandemic
Age 18years - 100years
Treatment Intervention group CoronaCope
Clinical Study IdentifierNCT04424212
SponsorLinkoeping University
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

Experience mental health problems that are caused or exacerbated by the corona pandemic and/or its consequences
years or older
Adequate ability to understand and speak Swedish
Access to the internet and a smartphone/computer

Exclusion Criteria

Other ongoing psychological treatment or counselling that interfere with trial treatment
Recent (within the past 3 months) changes in the dose of psychotropic medication
Any severe psychiatric or somatic conditions that would interfere with trial treatment
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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