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

NAActive, not recruitingINTERVENTIONAL
Enrollment

17,000

Participants

Timeline

Start Date

July 15, 2024

Primary Completion Date

July 14, 2026

Study Completion Date

July 14, 2026

Conditions
PTSD
Interventions
OTHER

PORTAL-PTSD

Patients will be eligible if they are 18+ years, have had a primary care visit in the last 2 years, and have not been screened for PTSD in the last year. The validated PC-PTSD-5 (Primary Care Post Traumatic Stress Disorder-5) screener will be used. Clinics will implement visit-based and population health screening for patients enrolled in the patient portal who have not been screened for PTSD in the last year and have had a clinic appointment in the last 2 years. The PCBH care manager or patient navigator will follow-up with patients every 2 weeks to ensure they have been connected to care and re-measure their PTSD symptoms. The follow-up calls will continue until symptom remission, after which follow-ups will occur quarterly for 6 months. Primary care clinicians will receive training on trauma-informed care and PTSD management, and will be surveyed at baseline, immediately after training, and 6 months-post intervention to evaluate changes in their knowledge of trauma-informed care.

Trial Locations (2)

60617

CFHC South Chicago, Chicago

60629

CFHC Chicago Lawn, Chicago

Sponsors
All Listed Sponsors
collaborator

Chicago Family Health Center

UNKNOWN

collaborator

National Institute on Minority Health and Health Disparities (NIMHD)

NIH

lead

University of Chicago

OTHER

NCT06479447 - Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder | Biotech Hunter | Biotech Hunter