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Clinical Trials/NCT04366011
NCT04366011
Completed
Not Applicable

Efficacy and Mechanisms of Psychosocial Treatments for Panic Disorder

Southern Methodist University1 site in 1 country40 target enrollmentNovember 2011
ConditionsPanic Disorder

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Panic Disorder
Sponsor
Southern Methodist University
Enrollment
40
Locations
1
Primary Endpoint
Panic Disorder Symptoms Severity change
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of the present study is to a) determine the comparative efficacy of the brief capnometry-assisted respiratory therapy (CART) and standard cognitive behavioural therapy (CBT), and b) to determine moderators and mediators.

With the data collected from the study, the investigators will test the following hypotheses: (a) CART will be as effective in treating PD/A as CBT, albeit in shorter time, b) patients with greater respiratory dysregulations, especially hyperventilation, at pretreatment will benefit more from CART, whereas patients with greater cognitive dysregulation will benefit more from CBT. CART, but not CBT, will result in reversal of hyperventilation.

Registry
clinicaltrials.gov
Start Date
November 2011
End Date
October 2015
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Heather McClary

Director of Research Compliance

Southern Methodist University

Eligibility Criteria

Inclusion Criteria

  • A current DSM-IV (Diagnostic and Statistical Manual IV) diagnosis of panic disorder with or without agoraphobia that is designated by the patient as the most important source of current distress
  • Patients must be willing to engage in exposure to fearful situations and sensations.

Exclusion Criteria

  • Diagnostic Exclusion Criteria:
  • A history of bipolar disorder, psychosis or delusional disorders (as evaluated by the SCID-IV-L (Structured Clinical Interview for the DSM IV) screening questions), substance abuse or dependence or alcohol abuse or dependence (other than nicotine in the last 3 months)
  • Medical exclusion factors:
  • Patients with severe unstable medical illness, clinically significant laboratory findings, or serious medical illness for which hospitalization may be likely within the next three months
  • Patients with a history of seizures, angina, myocardial infarction, congestive heart failure, clinically significant arrhythmias, transient ischemic attacks, cerebrovascular accidents, diabetes mellitus, significant asthma, emphysema, or chronic obstructive pulmonary disease

Outcomes

Primary Outcomes

Panic Disorder Symptoms Severity change

Time Frame: During treatment (weeks 1- 12) and 2-months and 6-months follow-ups

Panic Disorder Severity Scale (PDSS)

Secondary Outcomes

  • End-tidal PCO2 (carbon dioxide partial pressure) change(during treatment (weeks 1-12), 2 -and 6 months follow-up)

Study Sites (1)

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