MedPath

Psychodynamic Therapy for Treating Panic Disorder

Phase 2
Completed
Conditions
Panic Disorder
Interventions
Other: PFPP
Other: ART
Registration Number
NCT00128388
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

This study will determine the effectiveness of a manualized form of brief psychodynamic psychotherapy in comparison with applied relaxation training in treating adults with panic disorder.

Detailed Description

This is a randomized controlled trial of a manualized form of brief psychodynamic psychotherapy in comparison with applied relaxation training, a less active form of treatment in other studies, for adults with primary Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) panic disorder.

Forty nine patients who have signed written consent who have primary DSM-IV panic disorder have been entered into the study. Randomization has been stratified by presence of major depression and use of psychoactive, anti-panic medications. Medications, if present, have been held constant. All patients have received 24 sessions of either psychodynamic psychotherapy, or applied relaxation training for panic disorder. This study is currently closed for recruitment, although final follow-up assessments have yet to be completed.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
49
Inclusion Criteria
  • 18-55 years old
  • Primary DSM-IV panic disorder with or without agoraphobia
  • Severity 5/8 minimum on the Anxiety Disorders Interview Schedule
Exclusion Criteria
  • Psychosis
  • Unstable medication dosage
  • Unwilling to discontinue ongoing psychotherapy
  • Organic mental syndrome
  • Substance use or abuse

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1 PFPPPFPPPanic Focused Psychodynamic Psychotherapy
2 ARTARTApplied Relaxation Training
Primary Outcome Measures
NameTimeMethod
PDSS (panic disorder severity scale)termination, 2, 4, 6, 12 month f/u
Secondary Outcome Measures
NameTimeMethod
SDS (Sheehan disability scale)termination, 2, 4, 6, 12 month f/u
HARS (Hamilton anxiety rating scale)termination, 2, 4, 6, 12 month f/u
HDRS (Hamilton depression rating scale)termination, 2, 4, 6, 12 month f/u

Trial Locations

Locations (1)

Weill Medical College

🇺🇸

New York City, New York, United States

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