Internet-Delivered Cognitive Behaviour Therapy for Adolescent Depression

Not Applicable

Completed

• Conditions: Depression; Anxiety
• Interventions: Behavioral: Tailored Internet-administrated CBT-Treatment

• Registration Number: NCT02363205
• Lead Sponsor: Linkoeping University

Brief Summary

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.

Detailed Description

As above

Study Timeline

• Study Start: 2015-02
• Study First Submitted: 2015-02-09
• Study First Submitted QC: 2015-02-12
• Study First Posted: 2015-02-13
• Primary Completion: 2017-12
• Study Completion: 2017-12
• Status Verified: 2023-12
• Last Update Submitted: 2023-12-08
• Last Update Posted: 2023-12-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

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 & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
internet-delivered CBT	Tailored Internet-administrated CBT-Treatment	Tailored Internet-administrated CBT-Treatment

Primary Outcome Measures

Name	Time	Method
Beck Depression Inventory	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment, six months and 12 months post treatment.

Secondary Outcome Measures

Name	Time	Method
Beck Anxiety Inventory (BAI)	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment, six months and 12 months post treatment.
Knowledge of CBT strategies (developed by the research group)	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment, six months and 12 months post treatment.
Patient Health Questionnaire (PHQ)	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment
Social Interaction Anxiety Scale (SIAS)	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment, six months and 12 months post treatment.
The Mood and Feelings Questionnaire (MFQ)	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment, six months and 12 months post treatment.
The General Self-Efficacy Scale (GSE)	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment, six months and 12 months post treatment.
Subscale Life activites, WHO Disability Assessment Schedule 2.0 (WHODAS 2.0)	Baseline, post treatment, 6 months- and 12 months post treatment	Change from baseline to post treatment, six months and 12 months post treatment.

Trial Locations

Locations (1)

Linköping University; 🇸🇪 Linköping, Östergotland, Sweden