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Recruiting NCT06479447
Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder
Trial Parameters
Condition PTSD
Sponsor University of Chicago
Study Type INTERVENTIONAL
Phase N/A
Enrollment 17,000
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-07-15
Completion 2026-07-14
Interventions
PORTAL-PTSD
Brief Summary
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).
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