Internet-administrated Treatment of Anxiety Disorders

Not Applicable

Completed

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

• Registration Number: NCT01390168
• Lead Sponsor: Umeå University

Brief Summary

The purpose of this study is to determine whether tailored internet-administered cbt is a feasible treatment for anxiety disorders in clinical settings.

Detailed Description

Not available

Study Timeline

• Study Start: 2010-01
• Study First Submitted: 2011-07-01
• Study First Submitted QC: 2011-07-06
• Study First Posted: 2011-07-08
• Primary Completion: 2012-12
• Study Completion: 2012-12
• Status Verified: 2013-03
• Last Update Submitted: 2013-03-04
• Last Update Posted: 2013-03-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• over 18 years
• fulfill the criteria for at least one anxiety syndrome

Exclusion Criteria

• ongoing psychological treatment
• suicidal prone
• ongoing alcohol addiction

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
waitlist	Waitlist	waitlist
tailored internet-administrated CBT	Tailored Internet-administrated CBT-Treatment	Behavioral: tailored internet-administrated CBT

Primary Outcome Measures

Name	Time	Method
Change from baseline in Clinical Outcome in Routine Evaluation - Outcome Measure (CORE-OM)	Two weeks pre treatment (baseline), two weeks post treatment, and 12 months post treatment	Measures anxiety and depressive symptoms.; Change from baseline in anxiety and depressive symptoms expected between time frames.

Secondary Outcome Measures

Name	Time	Method
Change from baseline in Beck Anxiety Inventory (BAI)	Two weeks pre treatment (baseline), two weeks post treatment, 12 months post treatment	Measures anxiety symtoms.; Change from baseline in anxiety symptoms expected between time frames.
Change from baseline in Montgomery Åsberg Depression Rating Scale-Self Rated (MADRS-S)	Two weeks pre treatment (baseline), two weeks post treatment, and 12 months post treatment	Measures depressive symptoms.; Change from baseline in depressive symptoms expected between time frames.
Change from baseline in Quality of Life Inventory (QOLI)	Two weeks pre treatment (baseline), two weeks post treatment, and 12 months post treatment	Measures quality of life.; Change from baseline in quality of life expected between time frames.

Trial Locations

Locations (1)

Department of Behavioural Sciences and Learning, Linköping University; 🇸🇪 Linköping, Östergötland, Sweden