Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder
Recruiting
N/A
Interventional Study
PTSD
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 17,000 (estimated)
- Sponsor
- University of Chicago · Other
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About This Trial
This study aims to implement and evaluate a more timely approach to post-traumatic stress disorder (PTSD) diagnosis and management, entitled Patient Outcome Reporting for Timely Assessments of Life with Post-Traumatic Stress Disorder (PORTAL-PTSD) in a primary care setting with a high prevalence of trauma, specifically the South Side of Chicago, in partnership with Chicago Family Health Center (CF…
Trial Locations
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Eligibility Criteria
Patient Inclusion Criteria:
* Age ≥18 years
* Had an appointment at the study site in the last 24 months
* Were not screened for PTSD in the last 12 months
Exclusion Criteria:
* N/A
Contacts