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

Primary Purpose

Depression Symptoms, Anxiety Symptoms

Status
Active
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Internet-based Cognitive Behavioral Therapy
Sponsored by
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression Symptoms focused on measuring COVID-19, Corona, Postpandemic, Internet-based cognitive behavioral therapy (ICBT), Internet intervention, Depression, Anxiety

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept 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

Sites / Locations

  • Department of Behavioral Sciences and Learning, Linköping University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Treatment group

Control group

Arm 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.

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.

Outcomes

Primary Outcome Measures

Becks Depression Inventory-II
Measure of depressive symptoms. Range for the total sum is between 0 and 63 with a higher score indicating a higher level of depressive symptoms. Clinical ranges for minimal, mild, moderate and severe major depressive disorder are considered to be 0-13, 13-19, 20-28, and 29-63 points respectively.
Generalized Anxiety Disorder-7
Measure of anxiety symptoms and worry. When summing the points of the seven first questions, the scores are interpreted as mild, moderate and severe anxiety symptoms at 5-10, 11-15 and above 15 respectively.

Secondary Outcome Measures

Percieved Stress Scale-14
A questionnaire that aims to measure symptoms of stress. I contains 14 items that are scored on a range betewwn 0 (never) to 4 (very often). The total score range is between 0-56 and a higher score reflects higher levels of perceived stress.
Insonnia Severity Index
Measure of insomnia severity and symptoms of disordered sleep. Norm score ranges include low likelihood of sleep problems (0 to 7 points), some sleep problems (8 to 14 points), moderate sleep problems (15 to 21 points), severe sleep problems (22 to 28 points).
Short Health Anxiety Inventory-14
Measure of health anxiety, short version, with 14 items which are answered on a scale 0-3. This gives a total scare range of 0-42, where 0-14 indicate low probability of health anxiety, 15-17 is a grey zone and points over 18 indicates high probability for health anxiety.
Alcohol Use Disorder Identification Test
A 10-item screening tool to assess alcohol consumption, drinking behaviors, and alcohol-related problems. 10 items and scores ranging from 0-40 with higher scores indicating a higher level of alcohol use.
Karolinska Exhaustion Disorder Scale 9
A questionnaire aiming to measure fatigue and exhaustion. Maximum score is 54 and people scoring higher than 18 points are considered as being at risk for exhaustion syndrome.
Impact of Event Scale-6
A short version of Impact of Event Scale-R (IES-R), which assesses subjective distress caused by potentially traumatic events. It yields a total score between 0-24 with a higher score indicating more severe distress caused by the traumatic events.
UCLA loneliness scale 3
A short version of the UCLA loneliness scale, aiming to measure with three questions, for example "How often do you feel left out?" and are answered on a scale ranging from 1 (hardly ever) to 3 (often). People who gets the score 3-5 have been grouped as not lonely, while score 6-9 has been grouped as lonely.
Brunnsviken Brief Quality of Life Scale
Measure of quality of life with a total score ranging from 0 to 96 with a higher score indicating a higher quality of life. The scores of each of the six primary questions regarding perceived quality of life within an area of life are multiplied with the score of an item measuring the perceived importance of the area in question.
The Cognitive Failures Questionnaire
The measure contains 25 questions and are aiming to measure the experience of the frequency of misstakes one does in the every day life because of problems with attention, memory, and emotion regulation. Maximum score are 100, where higher score mirrors experienced problems to a greater extent.
InCharge Financial Distress/Financial Well-Being Scale
A measure aiming to measure distress related to the individual's economic situation. It contains of eight questions where the respondent gets to answer on a scale from 1 to 10.

Full Information

First Posted
December 16, 2022
Last Updated
October 4, 2023
Sponsor
Linkoeping University
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1. Study Identification

Unique Protocol Identification Number
NCT05656430
Brief Title
ICBT for Psychological Symptoms Related to the COVID-19 Pandemic Remaining After Societal Opening
Acronym
PCC
Official Title
Internet-based Cognitive Behavioral Therapy for Psychological Symptoms Related to the COVID-19 Pandemic Remaining After Societal Opening
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 1, 2023 (Actual)
Primary Completion Date
December 28, 2024 (Anticipated)
Study Completion Date
December 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Linkoeping University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression Symptoms, Anxiety Symptoms
Keywords
COVID-19, Corona, Postpandemic, Internet-based cognitive behavioral therapy (ICBT), Internet intervention, Depression, Anxiety

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
After recruitment finished, participants will be randomized to either intervention condition (treatment group) or control condition (wait list). Participants in the control group will receive the same treatment once the intervention group has finished the treatment and outcome measures has been collected.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment group
Arm Type
Experimental
Arm 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.
Arm Title
Control group
Arm Type
No Intervention
Arm 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.
Intervention Type
Behavioral
Intervention Name(s)
Internet-based Cognitive Behavioral Therapy
Intervention Description
Intervention based on cognitive behavioural therapy principles and adapted to the coronavirus pandemic situation. The 20 modules that the intervention consists of include psycho-educational texts as well as examples and exercises.
Primary Outcome Measure Information:
Title
Becks Depression Inventory-II
Description
Measure of depressive symptoms. Range for the total sum is between 0 and 63 with a higher score indicating a higher level of depressive symptoms. Clinical ranges for minimal, mild, moderate and severe major depressive disorder are considered to be 0-13, 13-19, 20-28, and 29-63 points respectively.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
Generalized Anxiety Disorder-7
Description
Measure of anxiety symptoms and worry. When summing the points of the seven first questions, the scores are interpreted as mild, moderate and severe anxiety symptoms at 5-10, 11-15 and above 15 respectively.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Secondary Outcome Measure Information:
Title
Percieved Stress Scale-14
Description
A questionnaire that aims to measure symptoms of stress. I contains 14 items that are scored on a range betewwn 0 (never) to 4 (very often). The total score range is between 0-56 and a higher score reflects higher levels of perceived stress.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
Insonnia Severity Index
Description
Measure of insomnia severity and symptoms of disordered sleep. Norm score ranges include low likelihood of sleep problems (0 to 7 points), some sleep problems (8 to 14 points), moderate sleep problems (15 to 21 points), severe sleep problems (22 to 28 points).
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
Short Health Anxiety Inventory-14
Description
Measure of health anxiety, short version, with 14 items which are answered on a scale 0-3. This gives a total scare range of 0-42, where 0-14 indicate low probability of health anxiety, 15-17 is a grey zone and points over 18 indicates high probability for health anxiety.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
Alcohol Use Disorder Identification Test
Description
A 10-item screening tool to assess alcohol consumption, drinking behaviors, and alcohol-related problems. 10 items and scores ranging from 0-40 with higher scores indicating a higher level of alcohol use.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
Karolinska Exhaustion Disorder Scale 9
Description
A questionnaire aiming to measure fatigue and exhaustion. Maximum score is 54 and people scoring higher than 18 points are considered as being at risk for exhaustion syndrome.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
Impact of Event Scale-6
Description
A short version of Impact of Event Scale-R (IES-R), which assesses subjective distress caused by potentially traumatic events. It yields a total score between 0-24 with a higher score indicating more severe distress caused by the traumatic events.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
UCLA loneliness scale 3
Description
A short version of the UCLA loneliness scale, aiming to measure with three questions, for example "How often do you feel left out?" and are answered on a scale ranging from 1 (hardly ever) to 3 (often). People who gets the score 3-5 have been grouped as not lonely, while score 6-9 has been grouped as lonely.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
Brunnsviken Brief Quality of Life Scale
Description
Measure of quality of life with a total score ranging from 0 to 96 with a higher score indicating a higher quality of life. The scores of each of the six primary questions regarding perceived quality of life within an area of life are multiplied with the score of an item measuring the perceived importance of the area in question.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
The Cognitive Failures Questionnaire
Description
The measure contains 25 questions and are aiming to measure the experience of the frequency of misstakes one does in the every day life because of problems with attention, memory, and emotion regulation. Maximum score are 100, where higher score mirrors experienced problems to a greater extent.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Title
InCharge Financial Distress/Financial Well-Being Scale
Description
A measure aiming to measure distress related to the individual's economic situation. It contains of eight questions where the respondent gets to answer on a scale from 1 to 10.
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.
Other Pre-specified Outcome Measures:
Title
Knowledge test
Description
Knowledge test about cognitive behavior therapy and how strategies in cognitive behavior therapy can be applied in every day situations. It consists of 16 questions and the respondent gets three answer options while one of the alternatives are correct. The respondent also gets to answer how confident he/she is about the answer (I'm guessing, I'm pretty certain, I'm quite certain).
Time Frame
Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerhard Andersson, PhD
Organizational Affiliation
Linkoeping University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Behavioral Sciences and Learning, Linköping University
City
Linköping
State/Province
Östergötland
ZIP/Postal Code
58183
Country
Sweden

12. IPD Sharing Statement

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

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