Early Functional Proprioceptive Stimulation Post-stroke
Recruiting now · Not applicable
Conditions studied: Stroke (CVA) or TIA
In brief
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.
Key facts
- Study ID
- NCT06192953
- Run by
- Centre Hospitalier Universitaire de Nice
- People needed
- 32
- Starts
- 2024-05-06
- Expected to finish
- 2027-04-30
- Last updated by the study team
- 2026-03-27
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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.
Where it is running
- CHU de Nice — Nice, France (enrolling)
Full record on ClinicalTrials.gov
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