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Clinical Trials/NCT00845260
NCT00845260CompletedPhase 3

Internet- Versus Group-Administered Cognitive Behavior Therapy for Panic Disorder in a Psychiatric Setting: A Randomized Equivalence Trial

Karolinska Institutet2 sites in 1 country113 target enrollmentStarted: December 2004Last updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
113
Locations
2
Primary Endpoint
Panic Disorder Severity Scale (PDSS)

Study Overview

Brief Summary

Panic Disorder with or without agoraphobia (PD/A) is a common, and unless it is treated, often chronic psychiatric disorder. The are effective pharmacological as well as psychological treatments for PD/A. Because of the lack of availability of the most effective psychological treatment, cognitive behavior therapy (CBT), self-help based CBT treatments have been developed. One of those are Internet-based CBT. The aim of this study is to compare the effectiveness of Internet and group CBT for PD/A in a regular psychiatric setting. 113 patients are consecutively and randomly assigned to either treatment (both lasting 10 weeks). The main outcome measure is the Panic Disorder Severity Scale(PDSS). The study hypothesis is that treatments will show equal effectiveness.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Primary Panic Disorder with or without Agoraphobia (PD/A)

Exclusion Criteria

  • active substance abuse
  • physiological etiology of panic symptoms
  • under 18 years of age
  • severe depression or suicidal ideation.
  • if on drugs for PD, not having had a constant dosage for 2 months
  • undergoing other cognitive behavioral treatment

Outcomes

Primary Outcomes

Panic Disorder Severity Scale (PDSS)

Time Frame: Pre, post at 6-month follow-up

Secondary Outcomes

  • Montgomery-Åsberg Depression Rating Scale (MADRS) Anxiety Sensitivity Index (ASI) Sheehan Disability Scale (SDS)(Pre, post and 6-month follow-up)

Investigators

Sponsor Class
Other

Study Sites (2)

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