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: 2026-03-26 @ 3:19 PM
Ignite Modification Date: 2026-03-26 @ 3:19 PM
NCT ID: NCT07483333
Eligibility Criteria: Inclusion Criteria: * Youth (aged 8-18 years) who received a SPIRIT program psychological trauma screening and were deemed clinically appropriate for SPIRIT group therapy. Clinically appropriate means the youth can historically engage in a group setting (e.g., school, camp, therapy group) without significant disruption to the group process or other participants. * Youth and parent/legal guardian are willing and able to provide informed consent/assent for randomization. * Youth and parent/legal guardian are fluent in English or Spanish. * Youth is not currently engaged in individual therapy at the time of enrollment (per patient/parent report). Exclusion Criteria: * Wards of the state or DCFS youth in care. * Youth with reported or observed symptoms that would significantly impair group therapy engagement, including but not limited to: intellectual disability, moderate-to-severe autism spectrum disorder, active suicidal ideation, uncontrolled psychosis, or other acute psychiatric symptoms that could disrupt the group process. * Regular use of alcohol or other substances that interfere with participation or disrupt the group process. * Youth requiring immediate higher-level psychiatric care (e.g., intensive outpatient programming, partial hospitalization, inpatient psychiatric admission, or residential treatment) at the time of first randomization.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 8 Years
Maximum Age: 18 Years
Study: NCT07483333
Study Brief:
Protocol Section: NCT07483333