Using Smart Phone Technology To Rural Veterans
USING SMART PHONE TECHNOLOGY AS A PLATFORM FOR DELIVERING MENTAL HEALTH CARE TO RURAL VETERANS
1 other identifier
interventional
15
1 country
1
Brief Summary
The purpose of this study is to see if a new Smart Phone application can help Veterans manage their panic symptoms after completing a two-day treatment for panic attacks.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 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
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2013
CompletedMay 2, 2011
April 1, 2011
2.1 years
April 29, 2011
April 29, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Panic Control Treatment (PCT)
A cognitive-behavioral therapy for PD that is highly efficacious, the standard delivery format of these sessions are typically offered once a week over a period of several months. This can pose challenges to rural Veterans who have multiple commitments and face long travel distances for mental health services. To improve accessibility to panic treatment, one innovative approach has been to deliver PCT in an intensive, two-day format.
2 days
Interventions
2 Day treatment for Panic Disorder
Eligibility Criteria
You may qualify if:
- Participants must
- be an Operation Enduring Freedom/Operation Iraqi Freedom/Operation New Dawn (OEF/OIF/OND) Veteran
- currently meet criteria for PD with or without Agoraphobia
- complete the weekend PD treatment at the Lufkin, Conroe or Texas City CBOC.
You may not qualify if:
- current substance dependence
- organic psychosis
- symptomatic bipolar disorder
- severe depression with suicidal intent or plan
- cognitive impairment (indicated by scores \<20 on SLUMS)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Michael E. DeBakey VA Medical Center
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
May 1, 2013
Study Completion
August 1, 2013
Last Updated
May 2, 2011
Record last verified: 2011-04