CClinicalTrials.gg
Status unknownNCT05673382Updated Oct 5, 2023

CrisisCope: ICBT for Psychological Symptoms Related to Life Crises.

An interventional study of Internet-based cognitive behavioral therapy in Depressive Symptoms and Anxiety Symptoms, sponsored by Linkoeping University. Status unknown at 1 site in Sweden. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-10-05.

Sponsored by Linkoeping University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Apr 2023), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The aim with this study is to investigate the effects of internet-based cognitive behavioral therapy (ICBT) on psychological symptoms related to one or more life crises. The target group is adults (18 years or older) who have symptoms of depression, anxiety, stress, or other psychological distress related to one or more life crises. The ICBT consists of eight modules during eight weeks with weekly support by a therapist and the treatment group will be compared to a wait-list control condition. Participants will be recruited in Sweden with nationwide recruitment.

Read the detailed description

The study is a randomized controlled trial about the effects of ICBT aiming to target psychological symptoms related to one or more life crises. Primary outcome measures are depressive 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 adaptability, stress symptoms, sleep problems, post traumatic stress symptoms and quality of life.

Because the psychological impact of a life crisis can be diverse, between different people and between different kinds of crises, a transdiagnostic individually tailored treatment will be used that has been tested in several previous trials. This treatment has been adopted to target psychological symptoms related to life crises.

02

Conditions studied

  • Depressive Symptoms
  • Anxiety Symptoms

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Keywords

  • Life crises
  • Randomized controlled trial
  • Internet-based cognitive behavioral therapy (ICBT)
  • Internet intervention
  • Depression
  • Anxiety
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's planned enrollment of 80 is close to the median of 84 across 6,720 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Linkoeping University is the lead sponsor of 189 studies on the registry; 40 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Experience psychological symptoms related to one or more life crises.
  • 18 years or older
  • Adequate ability to speak, read and write Swedish
  • Having access to the internet and a smartphone, computer or other device

Exclusion criteria

Exclusion Criteria:

  • Severe psychiatric or somatic issues that makes participation harder or impossible
  • Ongoing addiction
  • Acute suicidality
  • Other ongoing psychological treatment
  • Recent (within the past three months) changes in dose of psychotropic medication or planned change during the treatment weeks
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Treatment group

    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.

    Behavioral: Internet-based cognitive behavioral therapy

  • No intervention
    Control group

    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.

Interventions

  • BehavioralInternet-based cognitive behavioral therapy

    The intervention (the treatment) within this study is based on cognitive behavioral therapy principles and adapted to target psychological symptoms related to life crises. The 20 modules that the intervention consists of include psycho-educational texts as well as examples and exercises.

06

What researchers measure

Primary outcomes

  1. Beck Depression Inventory-II

    Measure of depressive symptoms. Range for the total sum is between 0 and 63 with a higher score 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, 14-19, 20-28, and 29-63 respectively.

    Time frame: Change between Baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.

  2. 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

    Time frame: Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.

Secondary outcomes

  1. Brief Adjustment Scale-6

    A measure of general psychological adjustment, consisting of six items. The items are on a seven-point response scale with higher scores indicating lower general psychological adjustment.

    Time frame: Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination. Also, every week during the treatment weeks.

  2. Patient Health Questionnaire-9

    Measure of depressive symptoms. Possible range for the total sum is 0 to 27 (created by summing up the scores from each item) with a higher score indicating higher levels of depression. Clinical cut-offs for mild, moderate, moderately severe and severe major depressive disorder are considered to be 5, 10, 15 and 20 respectively.

    Time frame: Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.

  3. Perceived Stress Scale-14

    A questionnaire that aims to measure symptoms of stress. It contains of 14 items that are scored on a range between 0 (never) and 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.

  4. Insomnia Severity Index

    Measure of insomnia severity and symptoms of disordered sleep. Norm score ranges include low likelihood of sleep problems (0-7 points), some sleep problems (8-14 points), moderate sleep problems (15-21 points), severe sleep problems (22-28 points).

    Time frame: Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.

  5. Alcohol Use Disorder Identification Test

    A ten-item scoring tool to assess alcohol consumption, drinking behaviors, and alcohol-related problems. Scores are 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.

  6. Impact of Events Scale-Revised

    Assesses subjective distress caused by traumatic events.Items are rated on a five-point scale from 0 (not at all) to 4 (extremely). Total score range between 0-88, 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.

  7. 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 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.

  8. InCharge Financial Distress/Financial Well-Being Scale

    A measure aiming to measure distress related to the individual's economic situation. It consists 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.

  9. Medical Outcome Study Social Support Survey

    A 12-item questionnaire aiming to measure the individual's perceived social support that is answered on a five-point scale (1-5). Besides the 12 items, the questionnaire also includes a question about how many family members and friends that the individual experience to have, who he/she can talk to. Total score range between 12 to 60.

    Time frame: Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.

  10. Posttraumatic Growths Inventory-Short form

    A questionnaire consisting of 10 items, aiming to investigate the individual's experience of positive change in relation to challenging life events. Each item are answered on a six-point scale ranging between 0 to 5, resulting in a total score range between 0-60.

    Time frame: Change between baseline, end of treatment after eight weeks and follow-up at 12 months after treatment termination.

07

Study locations

1 site
  • Department of Behavioral Sciences and Learning, Linköping University
    Linköping, Östergötland 58183, Sweden
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 5, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05673382
Lead sponsor
Linkoeping University
Responsible party
Gerhard Andersson (Professor, Linkoeping University) — Principal investigator
First posted
Jan 6, 2023
Start date
Jan 19, 2023
Primary completion
Apr 21, 2023
Completion
Jun 24, 2024 (estimated)
Last update
Oct 5, 2023

Study contacts

Gerhard Andersson, PhD
principal investigator · University Hospital, Linkoeping

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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