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 @ 4:23 AM
Ignite Modification Date: 2025-12-25 @ 4:23 AM
NCT ID: NCT02674620
Eligibility Criteria: Inclusion Criteria: * Must meet the diagnostic criteria of a concussion set forth by the Consensus Statement on Concussion in Sport 4th Annual Conference of Concussion in Sport, 2013 as determined by the treating neurosurgeon. * Presence of concussion-related symptoms at the time of testing. * Glasgow coma scale (GCS)=15 * Patients for who parental consent can be obtained. Exclusion Criteria: * Patients with a history of moderate or severe traumatic brain injury, epilepsy, or stroke. * Patients who have been diagnosed with a skull fracture, traumatic subarachnoid hemorrhage, subdural hematoma, epidural hematoma, intraparenchymal hemorrhage, or cerebral contusion on previous neuro-imaging studies. * Pregnant female patients. * GCS ≤ 14. * Patients with contraindications to exercise testing as assessed by PARmed-X assessment. * Patients for who parental consent can not be obtained.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 13 Years
Maximum Age: 19 Years
Study: NCT02674620
Study Brief:
Protocol Section: NCT02674620