Internet-Delivered Cognitive Behaviour Therapy for Adolescent Depression

Depression Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02363205
• Other study ID #: 2014/427-31
• Status: Completed
• Phase: N/A
• Start date: February 2015
• Est. completion date: December 2017

Study information

• Verified date: December 2023
• Source: Linkoeping University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

As above

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: December 2017
• Est. primary completion date: December 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 15 Years to 19 Years

Eligibility

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

Related Conditions & MeSH terms

• Anxiety
• Depression
• Depressive Disorder

Intervention

Behavioral:
• Tailored Internet-administrated CBT-Treatment
Guided internet-delivered CBT with chat sessions

Locations

Country	Name	City	State
Sweden	Linköping University	Linköping	Östergotland

Sponsors (1)

Lead Sponsor	Collaborator
Linkoeping University

Country where clinical trial is conducted

Sweden, 

Outcome

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