Skip to content

Evaluation of a Mobile Phone App for Veterans With PTSD

Evaluation of a Mobile Phone App for Veterans With PTSD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03199742
Enrollment
101
Registered
2017-06-27
Start date
2017-07-01
Completion date
2019-03-01
Last updated
2019-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress Disorders, Post-Traumatic, Veterans

Brief summary

The purpose of this study is to evaluate a mobile phone app designed to help Veterans with PTSD. Participants in this study will be randomized to receive one of 2 possible mobile phone apps. The term randomized means that which app a participant receives will not be based on any characteristic or behavior of the participant, but will be determined solely by chance like a flip of a coin.

Detailed description

Participants will receive access to the mobile app PTSD Coach. Participants will be randomized (by computerized coin flip) to one of two versions of the mobile app. All versions of the app will provide comprehensive information and tools for managing trauma symptoms, but one version of the app will provide personalized, confidential coaching messages delivered by either a Veteran peer or clinical psychologist. Participants will be asked to complete an online survey before using the mobile phone application and again 8 weeks later. Participants will be provided with the option to complete a telephone interview after 8 weeks of using the mobile phone application. To be eligible, participants must be a U.S. military Veteran, age 18 or older, have received a previous diagnosis of PTSD, and own an iPhone or iPad device.

Interventions

BEHAVIORALPersonalized App Coaching

All coaching messages will be based on how each participant responds to baseline survey questionnaires and how they interact with the experimental mobile phone application during the course of the study. Participants will be provided with feedback about recent progress & use of the app, information about coping strategies provided by the app, and a recommendation for making the best use of the app over the subsequent few days.

BEHAVIORALActive Comparator

Mobile phone application providing extensive information about PTSD and treatment, tools for managing PTSD symptoms, self-monitoring using the PTSD Checklist, and resources for obtaining support.

Sponsors

VA Palo Alto Health Care System
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Participants are randomized to receive one of 2 forms of the mobile phone application being tested in this study: with and without personalized coaching. Among those who receive coaching, participants will receive either peer-based coaching messages, clinician-based coaching messages, or automated messages.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* U.S. military Veteran * age 18 or older * previously diagnosed with PTSD * own an iPhone or iPad device

Exclusion criteria

* no previous history of PTSD

Design outcomes

Primary

MeasureTime frameDescription
PTSD Checklist 58 weeksMeasures symptoms of post-traumatic stress disorder
Functional Well-Being8 weeksMeasures functional well-being of Veterans across a number of domains, including self-care, romantic relationships, work, family functioning, and parenting. Subscale scores will be aggregated to create a summary score for this measure.
Engagement with the Application8 weeksObjectively-measured engagement with the intervention (# sessions)

Secondary

MeasureTime frameDescription
Self-Efficacy for Coping8 weeksSelf-efficacy for managing symptoms of PTSD using an author-constructed outcome measure.
Perceived Helpfulness of Intervention8 weeksHow helpful the intervention was for providing information and tools for managing PTSD.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026