RecruitingNot Applicable

Early Functional Proprioceptive Stimulation Post-stroke

France32 participantsStarted 2024-05-06

Plain-language 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.

Who can participate

Age range18 Years – 100 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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.

What they're measuring

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: Inclusion

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: Every week during 5 weeks maximum

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: 6 weeks

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: 10 weeks

Trial details

NCT IDNCT06192953

SponsorCentre Hospitalier Universitaire de Nice

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-01-31

Contact for this trial

Guillaume SACCO, MD

04 92 03 47 51 sacco.g@chu-nice.fr

View on ClinicalTrials.gov More Stroke (CVA) or TIA trials

Plain-language summary

Who can participate

Age range18 Years – 100 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: Inclusion

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: Every week during 5 weeks maximum

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: 6 weeks

Score at the Short Form of Postural Assessment Scale for Stroke Patients (SFPASS)

Timeframe: 10 weeks