We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Using Smart Phone Technology To Rural Veterans

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified April 2011 by Michael Debakey Veterans Affairs Medical Center.
Recruitment status was:  Not yet recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01346228
First Posted: May 2, 2011
Last Update Posted: May 2, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
South Central VA Mental Illness Research, Education & Clinical Center
Information provided by:
Michael Debakey Veterans Affairs Medical Center
  Purpose
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 Intervention
Panic Disorders Anxiety Disorders Behavioral: Panic Control Treatment (PCT)

Study Type: Interventional
Study Design: 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

Resource links provided by NLM:


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

Primary Outcome Measures:
  • Panic Control Treatment (PCT) [ Time Frame: 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.



Estimated Enrollment: 15
Study Start Date: April 2011
Estimated Study Completion Date: August 2013
Estimated Primary Completion Date: May 2013 (Final data collection date for primary outcome measure)
Intervention Details:
    Behavioral: Panic Control Treatment (PCT)
    2 Day treatment for Panic Disorder
    Other Names:
    • Panic Group
    • Weekend Panic Group
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.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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

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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01346228


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

Locations
United States, Texas
Michael E. DeBakey VA Medical Center Not yet recruiting
Houston, Texas, United States, 77030
Sponsors and Collaborators
Michael Debakey Veterans Affairs Medical Center
South Central VA Mental Illness Research, Education & Clinical Center
Investigators
Principal Investigator: Ellen Teng, Ph.D Michael E. DeBakey VA Medical Center
  More Information

Responsible Party: Ellen Teng, PhD., Michael E. DeBakey VA Medical Center
ClinicalTrials.gov Identifier: NCT01346228     History of Changes
Other Study ID Numbers: H-28199
First Submitted: April 29, 2011
First Posted: May 2, 2011
Last Update Posted: May 2, 2011
Last Verified: April 2011

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

Additional relevant MeSH terms:
Disease
Anxiety Disorders
Panic Disorder
Pathologic Processes
Mental Disorders