Actively Recruiting
Early Functional Proprioceptive Stimulation Post-stroke
Led by Centre Hospitalier Universitaire de Nice · Updated on 2026-03-27
32
Participants Needed
1
Research Sites
155 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The main objective of our study is to evaluate the impact of the use of Functional Proprioceptive Stimulation (FPS) on the recovery of the postural and motor functional capacities of the patient in the subacute phase of a stroke. The hypothesis is that the use of FPS has a positive impact on the recovery of the patient's functional abilities, as well as on the duration of treatment until the sit/stand transfers are completed. To evaluate this potential effect,there will be a randomization with two groups : one will have 5 sessions a week for 6 weeks maximum of SPF and the other groupe will have the same sessions but with the device stettled but not activated.
CONDITIONS
Official Title
Early Functional Proprioceptive Stimulation Post-stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient hospitalized at Cimiez University Hospital
- Ischemic or hemorrhagic cerebrovascular accident (CVA) of less than two weeks
- Hemiparesis requiring rehabilitation treatment
- Patient with a SFPASS score 64 6
- Patient affiliated to or beneficiary of a social security scheme
- Signature of informed consent
You will not qualify if you...
- NIHSS score greater than 20
- Muscle spasticity of the lower limbs requiring botulinum toxin injection
- Inability to understand rehabilitation instructions
- Vulnerable people
- Pregnant women, parturients and breastfeeding mothers
- Persons deprived of their liberty by judicial or administrative decision
- Persons hospitalized without consent
- Persons admitted to a health or social establishment for purposes other than research
- Adults subject to legal protection measures or unable to express consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
CHU de Nice
Nice, France
Actively Recruiting
Research Team
G
Guillaume SACCO, MD
CONTACT
J
Justine LEMAIRE
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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