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

Last updated: February 10, 2025
Sponsor: Laurent Servais
Overall Status: Active - Recruiting

Phase

N/A

Condition

Neurologic Disorders

Dystonias

Treatment

ActiMyo®/Syde®

Clinical Study ID

NCT06439823
MoCAP
  • Ages > 2
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Subjects over 2 years old

  • Male or female

  • Control subjects with no pathologies that have an impact on ambulation or motorfunction.

  • Signed informed consent and, in the case of minors, informed consent signed by theperson with parental authority/guardian

Exclusion

Exclusion Criteria:

  • Any other previous or present pathology having an impact on current motor or balancefunction

  • 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

Study Design

Total Participants: 200
Treatment Group(s): 1
Primary Treatment: ActiMyo®/Syde®
Phase:
Study Start date:
August 24, 2022
Estimated Completion Date:
August 31, 2028

Connect with a study center

  • CHR citadelle

    Liège, Liege 4000
    Belgium

    Active - Recruiting

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