Using Smart Phone Technology To Rural Veterans

Sponsor
Michael E. DeBakey VA Medical Center (U.S. Fed)
Overall Status
Unknown status
CT.gov ID
NCT01346228
Collaborator
South Central VA Mental Illness Research, Education & Clinical Center (U.S. Fed)
15
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28
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Panic Control Treatment (PCT)
N/A

Detailed Description

The first goal is to see how helpful the Smart Phone application is in helping veterans with panic symptoms continue to improve after you complete treatment.

The second goal of this study is to find out how much veterans like the Smart Phone application.

The third goal is to see how practical it is to use the Smart Phone application as a form of follow-up care. We want to see how much time is needed to provide technical support in using the application.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
USING SMART PHONE TECHNOLOGY AS A PLATFORM FOR DELIVERING MENTAL HEALTH CARE TO RURAL VETERANS
Study Start Date :
Apr 1, 2011
Anticipated Primary Completion Date :
May 1, 2013
Anticipated Study Completion Date :
Aug 1, 2013

Outcome Measures

Primary Outcome Measures

  1. Panic Control Treatment (PCT) [2 days]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Participants must

  1. be an Operation Enduring Freedom/Operation Iraqi Freedom/Operation New Dawn (OEF/OIF/OND) Veteran

  2. currently meet criteria for PD with or without Agoraphobia

  3. complete the weekend PD treatment at the Lufkin, Conroe or Texas City CBOC.

Exclusion Criteria:
  1. current substance dependence

  2. organic psychosis

  3. symptomatic bipolar disorder

  4. severe depression with suicidal intent or plan

  5. cognitive impairment (indicated by scores <20 on SLUMS)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Michael E. DeBakey VA Medical Center Houston Texas United States 77030

Sponsors and Collaborators

  • Michael E. DeBakey VA Medical Center
  • South Central VA Mental Illness Research, Education & Clinical Center

Investigators

  • Principal Investigator: Ellen Teng, Ph.D, Michael E. DeBakey VA Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01346228
Other Study ID Numbers:
  • H-28199
First Posted:
May 2, 2011
Last Update Posted:
May 2, 2011
Last Verified:
Apr 1, 2011
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 2, 2011