Back to resultsImproving Access To Services to Community Based Outpatient Clinics (CBOC's)
Primary Purpose
Panic Disorder
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Intensive Panic Control Treatment (IPCT)
Sponsored by
About this trial
This is an interventional treatment trial for Panic Disorder focused on measuring Panic, Anxiety
Eligibility Criteria
Inclusion Criteria:
- OEF/OIF/OND Veteran with current diagnosis of panic disorder with or without agoraphobia (presence of other anxiety disorders is acceptable)
Exclusion Criteria:
- Current substance dependence
- psychosis
- symptomatic bipolar disorder
- severe depression with suicidal intent or plan
Sites / Locations
- Michael E. DeBakey VA Medical Center and CBOC's (Lufkin, Texas City, and Conroe)Recruiting
Outcomes
Primary Outcome Measures
Intensive Panic Control Treatment (IPCT)
IPCT is a manualized treatment that consists of psychoeducation about panic disorder, behavioral exercises such as breathing retraining and interoceptive exposure to mimic symptoms during an actual panic attack, and cognitive restructuring (identifying thought distortions and replacing them with corrective thoughts based on realistic appraisals).
Secondary Outcome Measures
Full Information
NCT ID
NCT01346241
First Posted
April 29, 2011
Last Updated
April 29, 2011
Sponsor
Michael E. DeBakey VA Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01346241
Brief Title
Improving Access To Services to Community Based Outpatient Clinics (CBOC's)
Official Title
Improving Access To Services With An Intensive Two-Day Treatment For Panic
Study Type
Interventional
2. Study Status
Record Verification Date
April 2011
Overall Recruitment Status
Unknown status
Study Start Date
April 2011 (undefined)
Primary Completion Date
April 2013 (Anticipated)
Study Completion Date
April 2013 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Michael E. DeBakey VA Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to examine the feasibility of delivering IPCT in three rural VA community based outpatient clinics (CBOCs).
Detailed Description
We will first need to develop a more thorough understanding of the potential barriers associated with implementing this novel form of treatment in these settings by conducting focus groups at each facility. This information will then be used to modify the treatment, which will then be piloted with Veterans enrolled in these clinics who have panic disorder.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Panic Disorder
Keywords
Panic, Anxiety
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Intensive Panic Control Treatment (IPCT)
Other Intervention Name(s)
Panic Disorder
Intervention Description
A manualized treatment that consists of psychoeducation about panic disorder
Primary Outcome Measure Information:
Title
Intensive Panic Control Treatment (IPCT)
Description
IPCT is a manualized treatment that consists of psychoeducation about panic disorder, behavioral exercises such as breathing retraining and interoceptive exposure to mimic symptoms during an actual panic attack, and cognitive restructuring (identifying thought distortions and replacing them with corrective thoughts based on realistic appraisals).
Time Frame
3 Months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
OEF/OIF/OND Veteran with current diagnosis of panic disorder with or without agoraphobia (presence of other anxiety disorders is acceptable)
Exclusion Criteria:
Current substance dependence
psychosis
symptomatic bipolar disorder
severe depression with suicidal intent or plan
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ken Woods
Phone
713-791-1414
Ext
2247
Email
ken.woods@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ellen Teng, Ph.D
Organizational Affiliation
Michael E. DeBakey VA Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Michael E. DeBakey VA Medical Center and CBOC's (Lufkin, Texas City, and Conroe)
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ken Woods
Phone
713-791-1414
Ext
2247
Email
ken.woods@va.gov
12. IPD Sharing Statement
Learn more about this trial
Improving Access To Services to Community Based Outpatient Clinics (CBOC's)
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