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Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder

Who can join

Ages 18 and older · All sexes · Healthy volunteers welcome

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

About the study

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).

What is being tested

• PORTAL-PTSD (other)

Sponsor: University of Chicago · Participants: 17,000 · Started: Jul 15, 2024

Contact the study team

• Ainur Kagarmanova, MS, MA · Phone: 5742865712
• Erin Staab, MPH · Phone: 5072619859

Official record on ClinicalTrials.gov — NCT06479447

Locations in the U.S.

Conditions

• Post-Traumatic Stress Disorder

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.