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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02745834
Other study ID # IDF-1482-2014
Secondary ID
Status Recruiting
Phase N/A
First received March 15, 2016
Last updated April 19, 2016
Start date October 2015
Est. completion date October 2016

Study information

Verified date January 2016
Source Medical Corps, Israel Defense Force
Contact Shmuel Springer, PhD
Phone +972-584572869
Email shmuels@ariel.ac.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date October 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 40 Years
Eligibility 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.

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


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.

Locations

Country Name City State
Israel IDF Medical Corp Zrifin

Sponsors (2)

Lead Sponsor Collaborator
Medical Corps, Israel Defense Force Ariel University Center of Samaria

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stride time variability Coefficient of variance of the stride time, measured in % by the OPTOGait system Day 1 No
Primary Stride length variability Coefficient of variance of the stride length, measured in % by the OPTOGait system Day 1 No
Secondary Dual task general score 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). Day 1 No
See also
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Recruiting NCT06296537 - Effectiveness of Balance Training And Dynamic Neuromuscular Stabilization Training in Amateur Athletes With Chronic Ankle Instability N/A
Completed NCT02978365 - Factors Associated With Full Recovery After Surgical Repair of Shoulder Instability N/A
Completed NCT04644601 - Italian Version of The Cumberland Ankle Instability Tool (CAIT)