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Evaluation of PTSD Family Coach, a Mobile Phone App for Family Members of Individuals With PTSD

Stress Disorders, Post-Traumatic Clinical Trial

Official title:
Pilot Evaluation of PTSD Family Coach, a Mobile Phone App for Family Members of Individuals With PTSD

Clinical Trial Summary

The proposed pilot study is designed to test the feasibility, acceptability, and potential effectiveness of a mobile phone application (app) developed by the VA National Center for PTSD (VA NCPTSD) for use by family members of those with Posttraumatic Stress Disorder (PTSD). The primary objective of the proposed study is to assess whether family members of veterans with PTSD find the PTSD Family Coach app to be satisfactory and feasible to use. Secondary objectives are to determine if use of the app increases family members' self-efficacy and their ability to manage their own life stress, which may in part be the result of living with someone who has PTSD.

Clinical Trial Description

PTSD Family Coach is a mobile phone app for family members of individuals with PTSD. This application provides:

- education about PTSD

- a self-assessment tool measuring life stress

- self-management skills to address acute distress and stress

- direct connection to support and

- information about VA and community resources for family members of individuals with PTSD

From this research, the investigators wish to learn whether family members of someone with PTSD find the PTSD Family Coach to be satisfactory and feasible to use. The investigators would also like to know if use of the app increases family members' knowledge of PTSD, and its treatment, and their ability to manage their own life stress, which may in part be the result of living with a Veteran with PTSD.

Currently, there are very few resources for family members of Veterans with PTSD. If this research demonstrates that PTSD Family Coach is a promising tool for family members, it has the potential to address a tremendous unmet need using a very cost-effective, scalable solution. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02486705
Study type Interventional
Source VA Palo Alto Health Care System
Contact
Status Completed
Phase Phase 1
Start date January 2015
Completion date September 2015
View Details
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