Testing a proprioceptive stimulation method for stroke recovery in adults
Tests whether stimulation of body position sense helps adults recover movement after stroke.
Plain-language title generated from the registry record
Registry title: Early Functional Proprioceptive Stimulation Post-stroke
Key facts
- Where
- Nice, FranceSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 100 years old?
Source: NCT06192953, who can take part
Where in France
- CHU de NiceNice, FranceTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Centre Hospitalier Universitaire de Nice
- Trial code
- NCT06192953
- Record updated
- 27 March 2026
- Original description
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.Read full original descriptionShow less
Early Functional Proprioceptive Stimulation Post-stroke
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.
Inclusion: 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: 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.