Early Functional Proprioceptive Stimulation Post-stroke
- Conditions
- Stroke (CVA) or TIA
- Interventions
- Other: Functional Proprioceptive Stimulation
- Registration Number
- NCT06192953
- Lead Sponsor
- Centre Hospitalier Universitaire de Nice
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 32
- 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;
- Patient affiliated to or beneficiary of a social security scheme;
- Signature of informed consent
Exclusion criteria :
- NIHSS > 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 a judicial or administrative decision, persons hospitalized without consent and persons admitted to a health or social establishment for purposes other than research,
- Adults who are subject to a legal protection measure or who are unable to express their consent.
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Stimulated group Functional Proprioceptive Stimulation 5 sessions per week for 6 weeks maximum of reeducation with Functional Proprioceptive Stimulation
- Primary Outcome Measures
Name Time Method Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS) 10 weeks The SFPASS is a short instrument used to assess balance in lying, sitting and standing positions. It was designed specifically for stroke patients and is appropriate for all individuals, regardless of their postural performance. SFPASS focuses on mobility in bed and sitting to standing transfer. It is composed of 5 items rated on a 3-point scale with total scores ranging from 0 to 15 and is evaluated by a health professional.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
CHU de Nice
🇫🇷Nice, France