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 @ 1:50 PM
Ignite Modification Date:
2025-12-24 @ 1:50 PM
NCT ID:
NCT07254195
Eligibility Criteria:
Inclusion Criteria:
* Hospitalized for a first ischemic or hemorrhagic stroke
* Stroke occurrence more than 30 days prior
* Presenting motor deficits affecting the upper limb, with or without involvement of the lower limb
* Able to follow the instructions of the home program using the MindMotion GO device
* Having at home an accessible email address, an Internet connection with password, a smartphone, a screen or TV with HDMI input (Full HD 1080p resolution), and a free space of approximately 1 m x 2.5 m in front of the screen
* Ability to sit without assistance
* Patient agreeing to participate in the study by signing an informed consent form
* Affiliated with, or entitled to, a social security scheme
Exclusion Criteria:
History of stroke
* Neurological pathology other than stroke
* Patient with uncontrolled epilepsy or seizure disorder
* Cardiac disease limiting exercise
* Pain limiting rehabilitation dose
* Major comprehension problems or severe psychiatric and/or cognitive disorders that could compromise understanding of the protocol and the smooth running of the study.
* Uncorrected hearing or visual deficits
* Severe apraxia
* Severe memory impairment
* Severe unilateral spatial neglect
* Total plegia of affected limb
* Pregnant, parturient or breast-feeding women
* Persons deprived of their liberty by judicial or administrative decision
* Persons admitted to a health or social institution for purposes other than research
* Adults under legal protection (guardianship, curatorship)
* Subjects participating in other intervention research.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
85 Years
Study:
NCT07254195
Study Brief:
Protocol Section:
NCT07254195