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Clinical Trials/NCT01296321
NCT01296321
Unknown
Not Applicable

Tailored Internet-administrated Treatment of Panic Symptoms - A Randomised Controlled Trial

Linkoeping University0 sites57 target enrollmentFebruary 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety Disorders
Sponsor
Linkoeping University
Enrollment
57
Primary Endpoint
Panic Disorder Severity Scale (PDSS)
Last Updated
15 years ago

Overview

Brief Summary

The purpose of this study is to determine whether tailored internet-administrated CBT is a feasible approach in the treatment of panic symptoms and comorbid anxiety and depressive symptoms.

Registry
clinicaltrials.gov
Start Date
February 2010
End Date
April 2011
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Linkoeping University

Eligibility Criteria

Inclusion Criteria

  • Be between the ages of 18-30 years old or 31-46 years old
  • Have reoccurring panic attacks

Exclusion Criteria

  • Suicide prone
  • Alcohol addiction
  • Ongoing psychological treatment

Outcomes

Primary Outcomes

Panic Disorder Severity Scale (PDSS)

Time Frame: Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

Change from baseline in panic symptoms two weeks post treatment, at six months and at 12 months post treatment.

Secondary Outcomes

  • Clinical Outcome in Routine Evaluation - Outcome Measure (CORE-OM)(Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment)
  • Beck Anxiety Inventory (BAI)(Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment)
  • Montgomery Åsberg Depression Rating Scale-Self Rated (MADRS-S)(Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment)
  • Quality of Life Inventory (QOLI)(Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment)

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