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Clinical Trials/NCT02745834
NCT02745834
Unknown
Not Applicable

The Influence of Dual Task and Gait Speed on Gait Variability in Patients With Chronic Ankle Instability - a Case-control Study

Medical Corps, Israel Defense Force1 site in 1 country40 target enrollmentOctober 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Instability of Joint
Sponsor
Medical Corps, Israel Defense Force
Enrollment
40
Locations
1
Primary Endpoint
Stride length variability
Last Updated
10 years ago

Overview

Brief Summary

Case-control study to evaluate gait parameters during different conditions between patients who suffer from chronic ankle instability and healthy individuals.

Detailed Description

This case-control study will compare the different gait parameters such as stride time and stride length variability in different gait conditions (e.g., normal speed, normal speed with dual task, fast speed and fast speed with dual task) between healthy individuals and patients who suffer from chronic ankle instability. the measurements will be collected using the OPTOGait system installed on a treadmill.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
October 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Medical Corps, Israel Defense Force
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • history of at least one significant ankle sprain which occurred at least 12 months prior to enrolment in the study and was diagnosed by a physician or a physical therapist using clinical examination classifications described by Malliaropoulos et al
  • history of at least two episodes of 'giving way', and feelings of ankle joint instability in the previously injured ankle joint of 1 year post-initial sprain
  • the most recent injury occurred more than 6 weeks prior to the study enrolment
  • the ability to apply full weight bearing on the injured lower extremity with no more than mild discomfort

Exclusion Criteria

  • evidence of a concomitant injury (such as a bony injury or significant muscular/tendon injury)
  • previous ankle surgery
  • other pathological conditions or surgical procedures in lower extremity
  • neurological/vestibular or any other balance disorder.
  • The control group included healthy participants with no current or previous conditions that could affect proprioception.

Outcomes

Primary Outcomes

Stride length variability

Time Frame: Day 1

Coefficient of variance of the stride length, measured in % by the OPTOGait system

Stride time variability

Time Frame: Day 1

Coefficient of variance of the stride time, measured in % by the OPTOGait system

Secondary Outcomes

  • Dual task general score(Day 1)

Study Sites (1)

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