Immediate Effect of Postural Muscle's Vibrations on Gait in Chronic Vascular Hemiplegia

An inclusion medical exam will occur in order to explain the protocol to the patients, to receive their written informed consent and to check the inclusion and absence of non-inclusion criteria.

The study visit will happen in a 2 weeks' time span at most after the inclusion exam.

During the study visit, the patients will undergo:

• A quantitative gait analysis with Gait Rite and Optitrack before any intervention;
• Then, in a randomized order:

• A vibration stimulation on a non-postural muscle (biceps brachii muscle) in order to get a control stimulation (or "sham") with a new gait analysis with Gait Rite and Optitrack during the stimulation, then 2 and 10 minutes after it stopped,
• A vibration stimulation of the posterior neck muscles on the hemiplegic side, with a new gait analysis with Gait Rite and Optitrack during the stimulation, then 2 and 10 minutes after it stopped. The precise stimulation location will be located by the pressures centre deviation on a medio-lateral axis on a strength platform (this area can vary for a few centimetres from patient to patient),
• In order to assess the secondary outcome aiming at defining the best stimulation location, a vibration stimulation of the gluteus medius on the hemiplegic side, with a new gait analysis with Gait Rite and Optitrack during the stimulation, then 2 and 10 minutes after it stopped. In the same way than for the neck muscles, the scouting of the precise location will be assessed facing the greater trochanter by the pressures centre deviation on a medio-lateral axis on a strength platform.

The realisation of the entire protocol will last approximately 90 minutes.

At the end of the test, an optoelectronic recording by Optitrack will be realised on a treadmill in order to highlight potential differences between the gait on the ground and trained gait at comfortable speed for 2 minutes maximum.

Inclusion criteria

Hemiplegic subjects after stroke:

• Men or women aged over 18
• Stroke due to ischemic or haemorrhagic cause
• More than 6 months after stroke
• First episode of stroke
• Gait asymmetry before stimulation
• Able to walk more than 100 meters with or without cane
• Written informed consent

Exclusion criteria

• Orthopaedic or rheumatologic disorders impeding the good realisation of the measurement
• Adults under legal protective regimen or deprived of liberty