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 @ 1:58 PM
Ignite Modification Date:
2025-12-24 @ 1:58 PM
NCT ID:
NCT01574495
Eligibility Criteria:
Inclusion Criteria:
* adult (age \>18)
* survived a single cortical stroke at least 6 months previously involving ischemia or hemorrhage of the middle cerebral artery (MCA),
* demonstrated the presence of some active shoulder and elbow movement (characterized by Fugl-Meyer Assessment Upper Extremity scores ranging from 15-50 for ARM 1; 25-50 for ARM 2).
Exclusion Criteria:
* diffuse or multiple lesion sites or multiple stroke events
* bilateral paresis
* severe spasticity or contracture (Modified Ashworth ≥3
* severe concurrent medical problems
* severe sensory deficits
* cerebellar strokes resulting in severe ataxia
* significant shoulder pain
* focal tone management with Botulinim Toxin (Botox®) injection to the hemiparetic upper extremity (UE) within the previous four months,
* aphasia that would influence the ability to perform the experiment
* cognitive impairment (Mini Mental State Examination \< 23/30)
* affective dysfunction that would influence the ability to perform the experiment
* depth perception impairment (\< 3 on Stereo Circle Test)
* visual field cut or hemispatial neglect that would influence the ability to participate in the activity
* inability to provide informed consent
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01574495
Study Brief:
Protocol Section:
NCT01574495