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Clinical Trials/NCT02165787
NCT02165787
Completed
Not Applicable

Investigation of Gait Parameters in Health and Neurological Disease Under Varying Locomotor Conditions

University of Zurich1 site in 1 country208 target enrollmentApril 1, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gait Analysis in Neurological Disorders
Sponsor
University of Zurich
Enrollment
208
Locations
1
Primary Endpoint
Change of gait parameter after injury to CNS
Status
Completed
Last Updated
7 months ago

Overview

Brief Summary

In the cross-sectional component of this study, our overall objective is to gather a large pool of data from which we can generate gait "profiles". These profiles will consist of a constellation of gait (+/- electrophysiological) parameters associated with a particular neurological diagnosis or specific lesion(s) in neuroanatomical systems. Once developed, these profiles can be compared for differences and similarities; allowing insights into the specificity of the effect on gait of a given diagnosis or lesion in the case of the former and redundancy of neuroanatomical systems in that of the latter. A longitudinal component of the study will look at the evolution of gait parameters over time in a group of patients with spinal cord injury.

Registry
clinicaltrials.gov
Start Date
April 1, 2014
End Date
December 10, 2019
Last Updated
7 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age 18 - 80
  • written, informed consent
  • one of the following established diagnoses: unilateral stroke affecting motor system, Parkinson syndrome, cerebellar disease, vestibular dysfunction, spinal cord injury, multiple sclerosis
  • Brain and whole spine T1, T2 \& FLAIR magnetic resonance imaging performed within the last four months and available for study purposes or no contraindications to performing these scans
  • Healthy subjects:
  • age 18 - 80
  • written informed consent

Exclusion Criteria

  • Colour-blindness
  • Known to be pregnant or breastfeeding
  • Body mass index (weight in kg/height in metres squared) \>40 Unable to walk 50m within 6 minutes (with or without walking aids) Inability to undertake any component of the trial protocol
  • Terminal diagnosis with life expectancy less than six months
  • Cognitive disturbance defined as MMSE \< 25 Clinically significant comorbidities such as severe cardiovascular, pulmonary or malignant disease
  • Healthy subjects:
  • Colour-blindness
  • Known to be pregnant or breastfeeding
  • Body mass index (weight in kg/height in metres squared) \>40 Unable to walk 50m within 6 minutes
  • Reliance on walking aids / prostheses for mobilisation

Outcomes

Primary Outcomes

Change of gait parameter after injury to CNS

Time Frame: Timepoint 0 plus timepoint 6 months and 12 months

Study Sites (1)

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