Actively Recruiting
Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder
Led by University of Chicago · Updated on 2025-11-10
17000
Participants Needed
2
Research Sites
104 weeks
Total Duration
On this page
Sponsors
U
University of Chicago
Lead Sponsor
C
Chicago Family Health Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
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 (CFHC).
CONDITIONS
Official Title
Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Had an appointment at the study site in the last 24 months
- Were not screened for PTSD in the last 12 months
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 2 locations
1
CFHC South Chicago
Chicago, Illinois, United States, 60617
Actively Recruiting
2
CFHC Chicago Lawn
Chicago, Illinois, United States, 60629
Actively Recruiting
Research Team
A
Ainur Kagarmanova, MS, MA
CONTACT
E
Erin Staab, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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