Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06479447

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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