Actively Recruiting
Controlled Study of Upper and Lower Limb Movements in Patients with Pathologies Affecting Ambulation or Motor Function to Validate Signal Analysis Algorithms for Wearable Magneto-inertial Devices
Led by Laurent Servais · Updated on 2025-02-12
200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
L
Laurent Servais
Lead Sponsor
S
SYSNAV
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying upper and lower limb movements in people with conditions that affect walking or motor function, using wearable devices with magneto-inertial sensors. The goal is to validate algorithms that analyze signals from these sensors to reconstruct limb movements in both normal and pathological situations. This study includes patients with neuromuscular diseases and healthy control subjects to compare movement patterns. Participants will wear magneto-inertial sensors called ActiMyo4/Syde4 along with passive reflective markers from the MoCap4 motion capture system. They will undergo assessments of their upper and lower limbs performed by a neurologist or neuropediatrician in a walking laboratory setting. Each participant will have a single session during which their movements will be recorded and analyzed. During the study visit, participants will have their limb movements carefully examined and recorded using these advanced devices. Researchers will measure step length and distance over a period of 36 months as the main outcomes. This study involves only one session per participant, and all data collected will help improve movement analysis technology for people affected by neuromuscular diseases or motor impairments.
CONDITIONS
Brief Title
Controlled Study of Upper and Lower Limb Movements in Patients Patients with Pathologies That Have an Impact on Ambulation or Motor Function
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects over 2 years old
- Male or female
- Control subjects with no conditions affecting walking or motor function
- Signed informed consent; for minors, consent from parent or guardian
You will not qualify if you...
- Any other current or past condition affecting motor or balance function
- Recent surgery or trauma to upper or lower limbs within 6 months
- Control subjects who are athletes at national level or higher
- Pregnant or breastfeeding women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants are equipped with wearable magneto-inertial sensors and reflective markers to perform upper and lower limb assessments in a walking laboratory during a single session.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
CHR citadelle
Liège, Liege, Belgium, 4000
Actively Recruiting
Research Team
L
Laurie Medard
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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