Guided Internet-Delivered and Tailored Cognitive Behaviour Therapy for Adolescents With Depression: a Randomized Controlled Trial

Linkoeping University1 site in 1 country70 target enrollmentFebruary 2015

ConditionsDepression Anxiety

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Depression
Sponsor: Linkoeping University
Enrollment: 70
Locations: 1
Primary Endpoint: Beck Depression Inventory
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

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

Registry

clinicaltrials.gov

Start Date

February 2015

End Date

December 2017

Last Updated

2 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Linkoeping University

Responsible Party

Principal Investigator

Gerhard Andersson

Professor

Linkoeping University

Eligibility Criteria

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

Outcomes

Primary Outcomes

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.

Secondary Outcomes

Beck Anxiety Inventory (BAI)(Baseline, post treatment, 6 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)
Patient Health Questionnaire (PHQ)(Baseline, post treatment, 6 months- and 12 months post treatment)
Social Interaction Anxiety Scale (SIAS)(Baseline, post treatment, 6 months- and 12 months post treatment)
The Mood and Feelings Questionnaire (MFQ)(Baseline, post treatment, 6 months- and 12 months post treatment)
The General Self-Efficacy Scale (GSE)(Baseline, post treatment, 6 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)