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Improving Access To Services to Community Based Outpatient Clinics (CBOC's)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2011 by Michael Debakey Veterans Affairs Medical Center.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Michael Debakey Veterans Affairs Medical Center
ClinicalTrials.gov Identifier:
NCT01346241
First received: April 29, 2011
Last updated: NA
Last verified: April 2011
History: No changes posted
  Purpose

The purpose of this study is to examine the feasibility of delivering IPCT in three rural VA community based outpatient clinics (CBOCs).


Condition Intervention
Panic Disorder
 Behavioral: Intensive Panic Control Treatment (IPCT)

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Improving Access To Services With An Intensive Two-Day Treatment For Panic

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Michael Debakey Veterans Affairs Medical Center:

Primary Outcome Measures:
  • Intensive Panic Control Treatment (IPCT) [ Time Frame: 3 Months ] [ Designated as safety issue: No ]
    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).


Estimated Enrollment: 50
Study Start Date: April 2011
Estimated Study Completion Date: April 2013
Estimated Primary Completion Date: April 2013 (Final data collection date for primary outcome measure)
Intervention Details:
    Behavioral: Intensive Panic Control Treatment (IPCT)
    A manualized treatment that consists of psychoeducation about panic disorder
    Other Name: Panic Disorder
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.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01346241

Contacts
Contact: Ken Woods 713-791-1414 ext 2247 ken.woods@va.gov

Locations
United States, Texas
Michael E. DeBakey VA Medical Center and CBOC's (Lufkin, Texas City, and Conroe) Recruiting
Houston, Texas, United States, 77030
Contact: Ken Woods     713-791-1414 ext 2247     ken.woods@va.gov    
Sponsors and Collaborators
Michael Debakey Veterans Affairs Medical Center
Investigators
Principal Investigator: Ellen Teng, Ph.D Michael E. DeBakey VA Medical Center
  More Information

No publications provided

Responsible Party: Ellen Teng, Ph.D, Michael E. DeBakey VA Medical Center
ClinicalTrials.gov Identifier: NCT01346241     History of Changes
Other Study ID Numbers: H-28272
Study First Received: April 29, 2011
Last Updated: April 29, 2011
Health Authority: United States: Institutional Review Board

Keywords provided by Michael Debakey Veterans Affairs Medical Center:
Panic
Anxiety

Additional relevant MeSH terms:
Panic Disorder
Anxiety Disorders
Mental Disorders

ClinicalTrials.gov processed this record on May 19, 2013