About this trial
The main aim of the study is to validate the algorithms developed to analyze the signals from the various sensors contained in the magneto-inertial control units and reconstruct upper and lower limb movements under different normal and pathological conditions.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Subjects over 2 years old
Male or female
Control subjects with no pathologies that have an impact on ambulation or motor function.
Signed informed consent and, in the case of minors, informed consent signed by the person with parental authority/guardian
Disqualifiers
Any other previous or present pathology having an impact on current motor or balance function
Recent surgery or trauma to upper or lower limbs, or major surgery or trauma within 6 months of inclusion.
For control subjects, athlete of at least national level.
Pregnant or breast-feeding women
Trial design
Single group
Treatments tested in this trial
ActiMyo®/Syde®
DeviceSubjects will be equipped with magneto-inertial sensors (ActiMyo®/Syde®) and passive reflective markers belonging to the MoCap® motion capture system.
Treatment groups
Trial outcomes
Primary outcomes
step length and distance
Validate the algorithms developed to analyze the signals from the various sensors contained in magneto-inertial control units and reconstruct upper and lower limb movements.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Laurent Servais
Lead sponsor
Centre Hospitalier Universitaire de Liege
Sponsor institution
SYSNAV
Collaborator