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

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• 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

Locations
United States
Illinois
CFHC Chicago Lawn
RECRUITING
Chicago
CFHC South Chicago
RECRUITING
Chicago
Contact Information
Primary
Ainur Kagarmanova, MS, MA
akagarmanova@bsd.uchicago.edu
5742865712
Backup
Erin Staab, MPH
estaab@bsd.uchicago.edu
5072619859
Time Frame
Start Date: 2024-07-15
Estimated Completion Date: 2026-07-14
Participants
Target number of participants: 17000
Treatments
Experimental: PORTAL-PTSD Intervention
Chicago Family Health Center clinics are randomly assigned to any of the 5 steps. The PORTAL-PTSD intervention is implemented after clinic staff and clinicians have been trained.
No_intervention: No PORTAL-PTSD Intervention
Standard of care offered to all patients
Related Therapeutic Areas
Sponsors
Leads: University of Chicago
Collaborators: Chicago Family Health Center, National Institute on Minority Health and Health Disparities (NIMHD)

This content was sourced from clinicaltrials.gov