Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder
University of Chicago · with Chicago Family Health Center, National Institute on Minority Health and Health Disparities (NIMHD) · NCT06479447
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 17000
- US sites recruiting
- 2
- Study start
- July 15, 2024
- Record last updated
- November 10, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study 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).
Being studied: PORTAL-PTSD
Conditions: PTSD
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full 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
Recruiting US locations
CFHC South Chicago
Chicago, IL 60617
Site contact: Melissa Duplantis · 773-768-5000 · mduplantis@chicagofamilyhealth.org
CFHC Chicago Lawn
Chicago, IL 60629
Site contact: Melissa Duplantis, PsyD · 773-768-5000 · mduplantis@chicagofamilyhealth.org
Study contacts (from the official record)
- Ainur Kagarmanova, MS, MA · 5742865712 · akagarmanova@bsd.uchicago.edu
- Erin Staab, MPH · 5072619859 · estaab@bsd.uchicago.edu
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