Early Functional Proprioceptive Stimulation Post-stroke
ConditionStroke (CVA) or TIA
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-100
SponsorCentre Hospitalier Universitaire de Nice
About this trial
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.
Eligibility criteria
Qualifiers
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 ≤ 6;
Disqualifiers
NIHSS > 20;
Muscle spasticity of the lower limbs requiring botulinum toxin injection
Inability to understand rehabilitation instructions;
Vulnerable people
Trial design
Treatments tested in this trial
- Functional Proprioceptive Stimulation
Treatment groups
32 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov