Using Wearable Technology to Detect Symptoms of Posttraumatic Stress Disorder
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Posttraumatic Stress Disorder
- Sponsor
- Rush University Medical Center
- Enrollment
- 14
- Locations
- 1
- Primary Endpoint
- Clinician Administered PTSD Scale for DSM-5
- Status
- Terminated
- Last Updated
- 2 years ago
Overview
Brief Summary
The aim of the project is to advance our understanding of how individuals with Posttraumatic Stress Disorder (PTSD) experience symptoms in their every-day lives when they are in their home environment. To date, all PTSD assessments are retrospective; individuals with PTSD are asked to recount and report their symptoms over the past weeks or months. Such assessment procedures are negatively impacted by individuals' abilities to accurately recall information. Moreover, retrospective assessments provide little information about how symptoms are experienced in the moment and how these experiences then lead to other behaviors. The proposed project addresses these limitations by assessing PTSD symptoms and associated biological markers (e.g., sleep, heart rate, heart rate variability) in real-time by asking subjects to wear a smart device and complete brief surveys. Data will be collected from 50 individuals with PTSD and 20 healthy controls to help us better understand individuals' real-time experience with PTSD and lay the foundation to develop algorithms for possible in-the-moment interventions in the future.
Investigators
Philip Held
Research Director
Rush University Medical Center
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Clinician Administered PTSD Scale for DSM-5
Time Frame: Through study completion, average of 1 month
Clinician administered measure of PTSD
PTSD Checklist for DSM-5 Criteria
Time Frame: Through study completion, average of 1 month
Self-report measure of PTSD