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NCT01346228 Clinical Trial

Using Smart Phone Technology To Rural Veterans

Anxiety Disorders Clinical Trial

Official title:
USING SMART PHONE TECHNOLOGY AS A PLATFORM FOR DELIVERING MENTAL HEALTH CARE TO RURAL VETERANS

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01346228
Other study ID # H-28199
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 29, 2011
Last updated April 29, 2011
Start date April 2011
Est. completion date August 2013

Study information
Verified date April 2011
Source Michael Debakey Veterans Affairs Medical Center
Contact Ken Woods
Phone 713-791-1414
Email ken.woods@va.gov
Is FDA regulated No
Health authority United States: Federal GovernmentUnited States: Institutional Review Board
Study type Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 15
Est. completion date August 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 64 Years
Eligibility 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)

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Panic Control Treatment (PCT)
2 Day treatment for Panic Disorder

Locations
Country Name City State
United States Michael E. DeBakey VA Medical Center Houston Texas

Sponsors (2)
Lead Sponsor Collaborator
Michael Debakey Veterans Affairs Medical Center South Central VA Mental Illness Research, Education & Clinical Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary 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 No
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