ClinicalTrials.Veeva

Menu

ICBT for Psychological Symptoms Related to the COVID-19 Pandemic Remaining After Societal Opening (PCC)

L

Linköping University (LiU)

Status

Completed

Conditions

Depression Symptoms
Anxiety Symptoms

Treatments

Behavioral: Internet-based Cognitive Behavioral Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05656430
PostCoronaCope

Details and patient eligibility

About

This study aim to investigate the effects of internet-based cognitive behavioral therapy (ICBT) addressing psychological symptoms related to the COVID-19 pandemic and its consequences that remain after societal opening. The target group is adults (18 years or older) who still experience psychological symptoms related to the pandemic and the ICBT consists of eight modules during eight week with weekly support by a therapist. ICBT will be compared to a wait-list control condition. Participants will be recruited in Sweden with nationwide recruitment.

Full description

The study is a randomized controlled trial about the effects of ICBT regarding psychological symptoms related to the COVID-19 pandemic and its consequences remaining after societal opening. Primary outcome measures are depression symptoms (measured with Beck Depression Inventory-II) and anxiety symptoms (measured with Generalized Anxiety Disorder-7). Other outcome measures used will for example be about stress symptoms, sleep problems, post traumatic stress symptoms and quality of life.

Because of uncertainties about the psychological effects of COVID-19 pandemic, a transproblematic individually tailored treatment will be used that has been tested in several previous trials and adapted for addressing problems related to the pandemic and its consequences. The study (nor the recruitment within it) has not a focus on whether people have or have not been infected by the COVID-19 virus.

Enrollment

24 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Experience mental health problems related to the COVID-19 pandemic and/or its consecuences, which are still experienced as a problem (when the pandemic is not considered as dangerous to the society)
  • 18 years or older
  • Adequate ability to speak, read and write in Swedish
  • Having access to the internet and a smartphone, computer or other device

Exclusion criteria

  • Severe psychiatric or somatic issues that makes participation harder or impossible (which can include the diagnosis postcovid)
  • Ongoing addiction
  • Acute suicidality
  • Other ongoing psychological treatment
  • Recent (within the past 3 months) changes in the dose of psychotropic medication or planned change during the treatment weeks

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

24 participants in 2 patient groups

Treatment group
Experimental group
Description:
Eight weeks of individually tailored ICBT, were participants receives in total 8 modules out of 20 possible depending on their current problems and described situation with weekly support by a therapist.
Treatment:
Behavioral: Internet-based Cognitive Behavioral Therapy
Control group
No Intervention group
Description:
The control group is a wait-list control condition. Participants are instructed to wait. After the treatment group has finished their treatment and post-treatment measures has been collected, the control group receive the same treatment as the treatment group got.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems