Development Of a Virtual Stress Inoculation Training (SIT) Platform and Mobile Health App

Recruiting N/A Interventional Study
PTSD Trauma and Stressor Related Disorders Traumatic Brain Injury
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 79
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
The University of Texas Health Science Center, Houston · Other
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About This Trial
The purpose of this study is to demonstrate the feasibility and utility of SIT delivered asynchronously (self-paced) via fully virtual platform with and without the aid of a mobile health application and to determine initial change over baseline in terms of reduction in PTSD symptoms and improvement in resiliency in participants receiving the virtual SIT prototype, using Linear Mixed Models (LMMs)…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * US Military Veterans / Service Members * diagnosis of PTSD as measured by a Posttraumatic Symptom Checklist for DSM-5 (PCL-5) score of \>33 * history of combat trauma and/or military service in an imminent danger pay area * be fluent in English. * be capable of giving signed i…
Contacts

Sarah Jackson, PhD

(281) 825-9923

Sarah.E.Jackson@uth.tmc.edu

CONTACT