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Clinical Trials/NCT02231827
NCT02231827CompletedNot Applicable

A Study of the Balance Control During Gait : Comparison of Data Acquisition Between Force Plate and 3D Optoelectronic Gait Analysis System

University Hospital, Rouen1 site in 1 country50 target enrollmentStarted: October 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
50
Locations
1
Primary Endpoint
Braking of the center of mass index during gait initiation

Study Overview

Brief Summary

Gait and balance disorders are important public health problem necessitating studies to try to prevent falls. Many studies have dealt with spatiotemporal gait parameters or balance during quiet standing (posturography). Nevertheless, falls occurred predominantly during gait, and rarely during quiet standing. We have developed a tool to measure balance during gait : the braking of the center of mass (CM), a biomechanical parameter obtained from the vertical velocity of the CM recorded with a force plate.

In previous studies, we have shown that the braking of the CM was a physiological and a active mechanism, reflecting balance during gait. Unfortunately, the braking of the CM measured on a force plate provide an important intra-individual variability.

The 3D optoelectronic gait analysis system (VICON) also provide an estimation of the CM. The primary goal of this study is to compare intra-individual variability of the braking of the CM determined by a force plate or the 3D optoelectronic gait analysis system (VICON) in healthy subjects.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Healthy subjects
  • Between 20 and 40 years old
  • Effective contraception for women of childbearing age

Exclusion Criteria

  • Neurological, vestibular, rheumatologic, orthopaedic disorders, which could influence gait and balance.
  • Known spinal deformity
  • Severe visual impairment : visual acuity less than 6/10
  • Inability to stand and walk without assistance 15 meters
  • Subjects without social security
  • Subjects involved in another biomedical trial during this study
  • Pregnant or breastfeeding women

Arms & Interventions

Gait analysis

Experimental

Intervention: Gait analysis (Other)

Outcomes

Primary Outcomes

Braking of the center of mass index during gait initiation

Time Frame: 1 day

Braking of the center of mass (CM), a biomechanical parameter obtained from the vertical velocity of the CM, determined by a force plate or a 3D optoelectronic gait analysis system (VICON).

Secondary Outcomes

  • Braking of the center of mass index during locomotion(1 day)

Investigators

Sponsor
University Hospital, Rouen
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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