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:
2025-12-24 @ 12:24 PM
Ignite Modification Date:
2025-12-24 @ 12:24 PM
NCT ID:
NCT06354361
Eligibility Criteria:
Inclusion Criteria - participants must:
* be fluent in English
* reside in Ontario
* be public safety personnel (e.g. police officer, corrections officer, probation or parole officer, firefighter, search and rescue, paramedic, nurse, dispatcher)
* be able to provide written informed consent
* meet criteria on the PTSD Checklist for DSM-5 (PCL-5) for a provisional diagnosis of PTSD (cut-off score of \>30), administered during screening
* be able to attend regular online, 2-hour sessions once a week for 9 weeks, and be willing to complete the pre- and post- treatment assessments
* have access to a smart phone, tablet, or computer with a working microphone and camera, and have reliable and consistent internet
Exclusion Criteria:
* daily or almost daily use of benzodiazepines
* daily or almost daily use of narcotics
* diagnosed with alcohol use disorder OR substance use disorder in the past 12 months
* meet criteria on the Mini-International Neuropsychiatric Interview (M.I.N.I.) for diagnosis of alcohol use disorder OR substance use disorder
* history of moderate-to-severe brain injury and/or loss of consciousness with prolonged effects that interfere with daily functioning at school, work, or family unit
* history of neurological disorder(s) that may impact ability to participate in the study
* diagnosis of psychotic disorder(s) or bipolar disorder(s)
* diagnosis of neurodevelopmental disorder(s) that may impact ability to participate in the study
* other conditions/impairments/considerations that may interfere with completion of study tasks
* previous participation in Goal Management Training
* receiving treatment with anti-cholinergic medication, anti-psychotic medication, or psychostimulants
* had electroconvulsive therapy (ECT) within the past year
* currently engaged in a trauma-specific intervention that may impact the findings of the current study such as Eye Movement Desensitization and Reprocessing (EMDR), Cognitive Processing Therapy (CPT), Prolonged Exposure (PE), etc.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT06354361
Study Brief:
Protocol Section:
NCT06354361