Improving Access To Services to Community Based Outpatient Clinics (CBOC's)
Improving Access To Services With An Intensive Two-Day Treatment For Panic
1 other identifier
interventional
50
1 country
1
Brief Summary
The purpose of this study is to examine the feasibility of delivering IPCT in three rural VA community based outpatient clinics (CBOCs).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2011
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2011
CompletedFirst Submitted
Initial submission to the registry
April 29, 2011
CompletedFirst Posted
Study publicly available on registry
May 2, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2013
CompletedMay 2, 2011
April 1, 2011
2 years
April 29, 2011
April 29, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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).
3 Months
Interventions
A manualized treatment that consists of psychoeducation about panic disorder
Eligibility Criteria
You may qualify if:
- OEF/OIF/OND Veteran with current diagnosis of panic disorder with or without agoraphobia (presence of other anxiety disorders is acceptable)
You may not qualify if:
- Current substance dependence
- psychosis
- symptomatic bipolar disorder
- severe depression with suicidal intent or plan
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Michael E. DeBakey VA Medical Center and CBOC's (Lufkin, Texas City, and Conroe)
Houston, Texas, 77030, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ellen Teng, Ph.D
Michael E. DeBakey VA Medical Center
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- FED
Study Record Dates
First Submitted
April 29, 2011
First Posted
May 2, 2011
Study Start
April 1, 2011
Primary Completion
April 1, 2013
Study Completion
April 1, 2013
Last Updated
May 2, 2011
Record last verified: 2011-04