- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01346241
Improving Access To Services to Community Based Outpatient Clinics (CBOC's)
April 29, 2011 updated by: Michael E. DeBakey VA Medical Center
Improving Access To Services With An Intensive Two-Day Treatment For Panic
The purpose of this study is to examine the feasibility of delivering IPCT in three rural VA community based outpatient clinics (CBOCs).
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Anticipated)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ken Woods
- Phone Number: 2247 713-791-1414
- Email: ken.woods@va.gov
Study Locations
-
-
Texas
-
Houston, Texas, United States, 77030
- Recruiting
- Michael E. DeBakey VA Medical Center and CBOC's (Lufkin, Texas City, and Conroe)
-
Contact:
- Ken Woods
- Phone Number: 2247 713-791-1414
- Email: ken.woods@va.gov
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Intensive Panic Control Treatment (IPCT)
Time Frame: 3 Months
|
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).
|
3 Months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ellen Teng, Ph.D, Michael E. DeBakey VA Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2011
Primary Completion (Anticipated)
April 1, 2013
Study Completion (Anticipated)
April 1, 2013
Study Registration Dates
First Submitted
April 29, 2011
First Submitted That Met QC Criteria
April 29, 2011
First Posted (Estimate)
May 2, 2011
Study Record Updates
Last Update Posted (Estimate)
May 2, 2011
Last Update Submitted That Met QC Criteria
April 29, 2011
Last Verified
April 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-28272
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Panic Disorder
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