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 @ 12:56 AM
Ignite Modification Date:
2025-12-25 @ 12:56 AM
NCT ID:
NCT05511467
Eligibility Criteria:
INCLUSION CRITERIA
For all participants:
* adult volunteers (age ≥18 years)
* right-hand dominance as defined by the Edinburgh Handedness Inventory
Stroke-specific inclusion criteria:
* ischemic or hemorrhagic lesion
* subcortical or cortical tissue involvement
* chronic phase (\>6 months) after their index lesion
* voluntary whole-hand grip force (MRC, Medical Research Council scale for muscle force ≥2)
* repeated release (standardized as a reduction of 50% of maximum voluntary contraction measured with a dynamometer)
EXCLUSION CRITERIA
For all participants:
* Presence of any MRI risk factors
* substance use disorder
* psychotic disorders
Stroke-group specific exclusion criteria:
* Primary intracerebral hematoma
* subarachnoid hemorrhage
* bi-hemispheric or cerebellar strokes
* other concomitant neurological disorders affecting upper extremity motor function
* documented history of dementia before or after stroke
* severe aphasia, particularly of receptive nature (NIHSS Language subsection ≥2), affecting their ability to understand the purpose of the study and give informed consent
* uncontrolled hypertension despite treatment
* intake of tricyclic anti-depressants or neuroleptic medication.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05511467
Study Brief:
Protocol Section:
NCT05511467