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 @ 11:10 PM
Ignite Modification Date:
2025-12-24 @ 11:10 PM
NCT ID:
NCT01020669
Eligibility Criteria:
* INCLUSION CRITERIA:
1. Participants must be enrolled in the current UMB longitudinal study protocol.
2. All participants will be between 12 and 17 years old (inclusive).
3. All participants must be able to provide informed assent and have a parent/guardian who can provide informed consent.
EXCLUSION CRITERIA:
1. Report of a history of significant medical/neurological illness that might interfere with imaging data such as HIV positive status, cerebral vascular accident (CVA), central nervous system (CNS) tumor, head trauma, multiple sclerosis (MS) or other demyelinating diseases, epilepsy, or movement disorders.
2. Metallic devices in the body that preclude MRI scanning, as determined by self and parent (guardian) report.
3. Current use of psychotropic medication that may alter attentional functioning (e.g., Clonidine, antipsychotics, Effexor, stimulants).
4. Currently using respiratory, cardiovascular, anticonvulsant or other medications that might interfere with the mechanisms producing the BOLD signal.
5. Currently abusing street drugs as assessed by history and urine testing.
6. Pregnancy, which will be assessed by history during screening and by urine testing on scan days.
7. Claustrophobia by self and/or parent (guardian) report severe enough to preclude toleration of the scanning environment.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
13 Years
Maximum Age:
17 Years
Study:
NCT01020669
Study Brief:
Protocol Section:
NCT01020669