Actively Recruiting
Neuroplasticity After Proprioceptive Rehabiliation
Led by Institut National de la Santé Et de la Recherche Médicale, France · Updated on 2026-03-09
56
Participants Needed
1
Research Sites
234 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Sequences of muscle tendon vibrations allow to reproduce the sensory feedback during movement like locomotion and kinaesthesia. It is known that such a treatment promotes motor recovery after stroke assuming that it enhances neuroplasticity. The aim of the research is to study the activity in cerebrospinal circuitry to evaluate the neuroplastic changes during and after instrumented proprioceptive rehabilitation relying on sequences of muscle vibration in subacute stroke stages.
CONDITIONS
Official Title
Neuroplasticity After Proprioceptive Rehabiliation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hemiparesis at least transient in lower limb following an acquired brain injury (stroke or traumatic brain injury)
- French spoken
- Affiliated to a French social insurance
- No previous traumatic, vascular or neurodegenerative injuries
- Having presented during the acute phase or presenting a motor deficit of one of the lower limbs
- Presenting an absence of autonomy of walking at the entrance of the rehabilitation department
- In the sub-acute phase, i.e. from 15 days to 6 months after the accident
- Presenting moderate cognitive disorders allowing them to understand instructions and give their consent
You will not qualify if you...
- Strong cognitive disorders
- Maintenance of justice, tutelage, legal guardianship
- Pregnancy and breastfeeding
- Outpatients who do not have weekly follow-up in the rehabilitation department
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Pitié-Salpêtrière Hospital
Paris, France, 75013
Actively Recruiting
Research Team
V
Veronique Marchand-Pauvert, PhD
CONTACT
E
Eleonore Bayen, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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