The Influence of Dual Task and Gait Speed on Gait Variability in Patients With Chronic Ankle Instability

Sponsor
Medical Corps, Israel Defense Force (Other)
Overall Status
Unknown status
CT.gov ID
NCT02745834
Collaborator
Ariel University (Other)
40
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2
12
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Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Gait analysis
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
The Influence of Dual Task and Gait Speed on Gait Variability in Patients With Chronic Ankle Instability - a Case-control Study
Study Start Date :
Oct 1, 2015
Anticipated Primary Completion Date :
May 1, 2016
Anticipated Study Completion Date :
Oct 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Chronic Ankle Instability

Soldiers who suffer from chronic ankle instability who had a first major ankle sprain one year or more ago, and did not sustained any major ankle sprain in the last two months, will go through Gait analysis intervention.

Other: Gait analysis
Gait will be analysed while participants will walk on a treadmill at different self selected speeds, using the OPTOGait system. Spatiotemporal measures are collected without the use of any markers.

Experimental: Healthy controls

Healthy soldiers who are not suffering from chronic ankle instability, will go through Gait analysis intervention.

Other: Gait analysis
Gait will be analysed while participants will walk on a treadmill at different self selected speeds, using the OPTOGait system. Spatiotemporal measures are collected without the use of any markers.

Outcome Measures

Primary Outcome Measures

  1. Stride time variability [Day 1]

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

  2. Stride length variability [Day 1]

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

Secondary Outcome Measures

  1. Dual task general score [Day 1]

    Participants will be asked to count backward, reducing 7 at a time, starting at different 3 digits number. The outcome measure is a calculation of the number of total answers multiple by (number of correct answers - number of wrong answers).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 IDF Medical Corp Zrifin Israel

Sponsors and Collaborators

  • Medical Corps, Israel Defense Force
  • Ariel University

Investigators

  • Principal Investigator: Shmuel Springer, PhD, Researcher

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical Corps, Israel Defense Force
ClinicalTrials.gov Identifier:
NCT02745834
Other Study ID Numbers:
  • IDF-1482-2014
First Posted:
Apr 20, 2016
Last Update Posted:
Apr 20, 2016
Last Verified:
Jan 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 20, 2016