Controlled Study of Upper and Lower Limb Movements in Patients Patients with Pathologies That Have an Impact on Ambulation or Motor Function
NCT ID: NCT06439823
Last Updated: 2025-02-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
200 participants
INTERVENTIONAL
2022-08-24
2028-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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Patient with neuromuscular disease or control subjects
Patients and controls will be examined by a neuropediatric or neurologist. they will perform upper and lower limb assessments in a walking laboratory. this study comprises a single session per patient/control subject.
ActiMyo®/Syde®
Subjects will be equipped with magneto-inertial sensors (ActiMyo®/Syde®) and passive reflective markers belonging to the MoCap® motion capture system.
Interventions
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ActiMyo®/Syde®
Subjects will be equipped with magneto-inertial sensors (ActiMyo®/Syde®) and passive reflective markers belonging to the MoCap® motion capture system.
Eligibility Criteria
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Inclusion Criteria
* 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
Exclusion Criteria
* 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
2 Years
ALL
Yes
Sponsors
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SYSNAV
INDUSTRY
Laurent Servais
OTHER
Responsible Party
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Laurent Servais
Professor Laurent Servais
Locations
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CHR citadelle
Liège, Liege, Belgium
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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MoCAP
Identifier Type: -
Identifier Source: org_study_id
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