Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 1:31 AM
Ignite Modification Date: 2025-12-25 @ 1:31 AM
NCT ID: NCT06618794
Eligibility Criteria: Inclusion Criteria: * Treatment for a violent injury at the University of Chicago Trauma Center * Ages 14-64 years * Able to provide informed consent (18 years and older) or assent (14-17 years) Inclusion of women and minorities: This research proposal includes women and ethnic minorities. Patient participants will be primarily non-Hispanic Black or Hispanic race and ethnicity. The study expects participants to be proportional to the population-wide estimates for the South Side community. The majority will be low-income with variable functional health literacy. These characteristics are representative of the target population and describe the population most likely to benefit from the proposed study. Youth stakeholder participants will be multi-ethnic and racially diverse. Inclusion of children: This study will include children ages 14-17 years old, based on Illinois state labor laws for child employment, as well as the ages of youth who are primarily treated for penetrating injury at the UCMC trauma center. This age is also a pragmatic cutoff for children providing meaningful input on community and healthcare solutions to violence. Exclusion Criteria: * Diagnosis of severe mental illness (i.e., psychotic disorder, schizophrenia, suicidality) * Unable to provide informed consent due to mental status * Prior receipt of legal services at UCMC within the past year * Currently imprisoned or incarcerated * Residing at an Indiana address.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 14 Years
Maximum Age: 64 Years
Study: NCT06618794
Study Brief:
Protocol Section: NCT06618794