Study of limb movements in patients with neuromuscular diseases
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
This study is testing new technology to see how well it can track and understand limb movements in people with neuromuscular diseases compared to those without any movement issues.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 2 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire de Liege Academic / other |
| Locations | 1 site (Liège, Liege) |
| Trial ID | NCT06439823 on ClinicalTrials.gov |
What this trial studies
This study aims to validate algorithms that analyze signals from sensors in magneto-inertial control units to reconstruct upper and lower limb movements in patients with neuromuscular diseases. It involves both patients with these conditions and control subjects without any motor function impairments. The study will assess movement patterns under various conditions to improve understanding of motor function and ambulation. The interventions used in this study include ActiMyo® and Syde®.
Who should consider this trial
Good fit: Ideal candidates include individuals over 2 years old with neuromuscular diseases affecting their motor function.
Not a fit: Patients with other pathologies affecting motor function or recent surgeries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding and treatment of motor function impairments in patients with neuromuscular diseases.
How similar studies have performed: While similar studies have explored sensor-based movement analysis, the specific algorithms and approach in this study may be novel.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Liège, Liege
- CHR citadelle — Liège, Liege, Belgium (Recruiting)
Study contacts
- Study coordinator: Laurie Medard
- Email: laurie.medard@citadelle.be
- Phone: 003243218222
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.