- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02363205
Internet-Delivered Cognitive Behaviour Therapy for Adolescent Depression
December 8, 2023 updated by: Gerhard Andersson, Linkoeping University
Guided Internet-Delivered and Tailored Cognitive Behaviour Therapy for Adolescents With Depression: a Randomized Controlled Trial
The purpose of this study is to determine whether tailored internet-administrated cognitive behaviour therapy (CBT) is a feasible approach in the treatment of depressive symptoms and comorbid anxiety symptoms.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
As above
Study Type
Interventional
Enrollment (Actual)
70
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Östergotland
-
Linköping, Östergotland, Sweden, 58183
- Linköping University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
15 years to 19 years (Child, Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Be between the ages of 15-19 years old
- Have symptoms of depression, major depression
Exclusion Criteria:
- Suicidal ideation
- Alcohol addiction
- other major primary psychiatric disorder
- Ongoing psychological treatment
- recent (during last 4 weeks) change in psychiatric medication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: control
Weekly check-up
|
|
|
Experimental: internet-delivered CBT
Tailored Internet-administrated CBT-Treatment
|
Guided internet-delivered CBT with chat sessions
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Beck Depression Inventory
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment, six months and 12 months post treatment.
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Beck Anxiety Inventory (BAI)
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment, six months and 12 months post treatment.
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
|
Social Interaction Anxiety Scale (SIAS)
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment, six months and 12 months post treatment.
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
|
The General Self-Efficacy Scale (GSE)
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment, six months and 12 months post treatment.
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
|
Subscale Life activites, WHO Disability Assessment Schedule 2.0 (WHODAS 2.0)
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment, six months and 12 months post treatment.
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
|
Knowledge of CBT strategies (developed by the research group)
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment, six months and 12 months post treatment.
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
|
Patient Health Questionnaire (PHQ)
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
|
The Mood and Feelings Questionnaire (MFQ)
Time Frame: Baseline, post treatment, 6 months- and 12 months post treatment
|
Change from baseline to post treatment, six months and 12 months post treatment.
|
Baseline, post treatment, 6 months- and 12 months post treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gerhard Andersson, Linkoeping University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2015
Primary Completion (Actual)
December 1, 2017
Study Completion (Actual)
December 1, 2017
Study Registration Dates
First Submitted
February 9, 2015
First Submitted That Met QC Criteria
February 12, 2015
First Posted (Estimated)
February 13, 2015
Study Record Updates
Last Update Posted (Estimated)
December 11, 2023
Last Update Submitted That Met QC Criteria
December 8, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2014/427-31
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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