Controlled Study of Upper and Lower Limb Movements in Patients Patients with Pathologies That Have an Impact on Ambulation or Motor Function
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: ActiMyo®/Syde®.
- Who it may be relevant to
- Registry conditions: Neuromuscular Diseases. Basic parameters: from 2 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Belgium
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Controlled Study of Upper and Lower Limb Movements in Patients Patients with Pathologies That Have an Impact on Ambulation or Motor Function to Validate Signal Analysis Algorithms for Wearable Devices Using Magneto-inertial Technology
Overview
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.
Interventions
- Device ActiMyo®/Syde®
Subjects will be equipped with magneto-inertial sensors (ActiMyo®/Syde®) and passive reflective markers belonging to the MoCap® motion capture system.
Primary outcome measures
- step length and distance [Time frame: 36 months]
Eligibility criteria
Inclusion criteria
- 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
Exclusion criteria
- 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Basic science
Study locations
Belgium · 1 center
- CHR citadelle — Liège
Identifiers
NCT: NCT06439823 · MoCAP