NCT06192953Recruiting
Early Functional Proprioceptive Stimulation Post-stroke
Source: ClinicalTrials.gov · Last updated 27 Mar 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 32 (estimated)
- First submitted
- 11 Dec 2023
- Start date
- 6 May 2024
- Primary completion date
- 31 Jan 2027
- Lead sponsor
- Centre Hospitalier Universitaire de Nice
- Diseases
- Stroke
- NCT number
- NCT06192953
What you commit to
- Study type: Interventional
- Planned participants: 32
- From 6 May 2024 to the primary completion date, 31 Jan 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- 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.
Who the study is looking for
- 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
Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU de Nice Coordinator of this site? Confirm its status | Nice | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.