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Clinical Trials/NCT00063375
NCT00063375
Completed
Phase 1

Interactive Computer Treatment for Panic Disorder

Florida State University1 site in 1 country60 target enrollmentJanuary 2002
ConditionsPanic Disorder

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Panic Disorder
Sponsor
Florida State University
Enrollment
60
Locations
1
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This study will develop an interactive computer-based version of cognitive behavioral therapy (CBT) and compare its effectiveness to book-based CBT for the treatment of panic disorder.

Detailed Description

Panic disorder (PD) is a highly prevalent and debilitating condition. Unfortunately, many people with PD go untreated because of the high cost and low availability of treatment. Research shows that CBT is an effective treatment for PD. When administered as a self-help, computer based treatment, CBT may provide a less expensive, more engaging treatment for PD. Participants in this study will be randomly assigned to receive computer based treatment, book based treatment, or no treatment for 10 weeks. After these 10 weeks, symptoms of anxiety and depression will be measured with patient interviews, scales, and questionnaires.

Registry
clinicaltrials.gov
Start Date
January 2002
End Date
February 2007
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Norman Schmidt

Professor

Florida State University

Eligibility Criteria

Inclusion Criteria

  • DSM-IV diagnosis of panic disorder, with or without agoraphobia

Exclusion Criteria

  • Change in medication type or dose 12 weeks prior to study entry
  • Current substance abuse
  • Current or past schizophrenia, bipolar disorder, or organic mental disorder. Patients on medications must meet stability requirements such that initial administration of the medication and dose has been maintained for at least 3 months prior to treatment and will be maintained until post-treatment.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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