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:
2025-12-26 @ 10:44 PM
Ignite Modification Date:
2025-12-26 @ 10:44 PM
NCT ID:
NCT05945212
Eligibility Criteria:
Inclusion Criteria:
* Stroke patients in subacute rehabilitation phase (between 14 days and 3 months post-stroke)
* Presenting with a stroke, ischemic or hemorrhagic
* Lower-limb deficiency with an initial motor testing \< 4 according to the MRC scale
* No neurological history with functional impact other than stroke
* Having received informed information about the study and having signed the written consent
* Affiliated or entitled to a social security scheme.
* Patients under guardianship may be included; they may give their consent with the assistance of their guardian.
If the participant is unable to write, their consent may be given and documented by other appropriate means in the presence of at least one impartial witness. In this case, the witness will sign and date the informed consent document.
Exclusion Criteria:
* Multiple stroke
* Other neurological, cognitive or psychiatric conditions
* Orthopedic ankle history compromising measurements
* Botulinum toxin injected in the lower limb prior the study protocol
* Patient with phlebitis or risk of thrombosis in the lower limb
* Patient under tutorship
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT05945212
Study Brief:
Protocol Section:
NCT05945212