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Early Functional Proprioceptive Stimulation Post-stroke — StimProF  

Stroke (CVA) or TIA Clinical Trial

Official title:
Early Functional Proprioceptive Stimulation Post-stroke

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06192953
Study type Interventional
Source Centre Hospitalier Universitaire de Nice
Contact Guillaume SACCO, MD
Phone 04 92 03 47 51
Email sacco.g@chu-nice.fr
Status Recruiting
Phase N/A
Start date May 6, 2024
Completion date April 30, 2025
View Details
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