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Controlled Study of Upper and Lower Limb Movements in Patients Patients with Pathologies That Have an Impact on Ambulation or Motor Function

L

Laurent Servais

Status

Enrolling

Conditions

Neuromuscular Diseases

Treatments

Device: ActiMyo®/Syde®

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

2+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Patient with neuromuscular disease or control subjects
Experimental group
Description:
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.
Treatment:
Device: ActiMyo®/Syde®

Trial contacts and locations

1

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Central trial contact

Laurie Medard

Data sourced from clinicaltrials.gov

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