Recruiting

PORTAL-PTSD

Sponsor:

University of Chicago

Code:

NCT06479447

Conditions

PTSD

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

PORTAL-PTSD

Study Details

Brief 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).

Conditions

PTSD

Study ID

NCT06479447

Start date

Jul 15, 2024

Status verified date

May, 2025

Completion date

Jul 14, 2026

Anticipated

Primary completion date

Jul 14, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

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

Study Design

Enrollment

17000 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

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

Interventions

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.

Primary outcome measure

  • PTSD screening rates [ Time Frame: every 6 months post-intervention for 2 years ]
  • PTSD diagnoses rates [ Time Frame: every 6 months post-intervention for 2 years ]
  • PTSD prescribed treatment rates [ Time Frame: every 6 months post-intervention for 2 years ]
  • PTSD symptoms severity [ Time Frame: every 6 months post-intervention for 2 years ]

Central Contacts and Locations

Central contacts

Locations

CFHC South Chicago

Recruiting

Chicago, Illinois, United States, 60617

Contacts

CFHC Chicago Lawn

Recruiting

Chicago, Illinois, United States, 60629

Contacts

More Information

Sponsor

University of Chicago

Last update posted

Nov 10, 2025

Last verified

May, 2025

Keywords

  • behavioral health
  • PTSD
  • PTSD screening

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Chicago on 2025-11-10.