Kinematic Parameters of Running in Individuals With Pronated Foot

November 26, 2018 updated by: Gali Dar, University of Haifa
The aim of the study is to examine the kinematic parameters of individuals with pronated foot compared with individuals with normal foot

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Individual with and without pronated foot will be recruited. Pronation will be defined according to navicular drop test. Inclusion criteria : individual who run on a regular basis at least 3 times per week for one hour, can run 5 Km in less then 40 minutes, without past injuries during the last year of Achilles tendon or other lower extremities pain.

Individuals will be asked to run for 5 Km in self selected velocity. The Milestone pod device will be used to monitor kinematic parameters.

functional test will be conducted before and after the running as follows: heel raise test and one leg hop for distance test.

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Israel
      • Haifa, Israel
        • University of Haifa

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 50 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • running on a daily basis at least 3 times per week with minimum of 1 hour
  • capable to run 5 km in less then 40 minutes
  • willing to participate in the study

Exclusion Criteria:

  • previous surgery in lower extremities
  • Achilles tendon pain during the last year

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Screening
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: pronated group
individuals with pronated foot
Diagnostic test: running
individuals will be asked to run for 5 km in self selected speed
Other Names:
  • kinematic parameters of running
Active Comparator: control group
individuals with normal foot posture
Diagnostic test: running
individuals will be asked to run for 5 km in self selected speed
Other Names:
  • kinematic parameters of running

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
stride length
Time Frame: up to 6 months
stride length in cm
up to 6 months
cadence
Time Frame: up to 6 months
steps per minute
up to 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
velocity
Time Frame: up to 6 months
running velocity in Km/hour
up to 6 months
heel raise test
Time Frame: up to 6 months
how many good heel raise till fatigue
up to 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Haifa

Investigators

  • Principal Investigator: Gali Dar, PHd, University of Haifa

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 22, 2018

Primary Completion (Actual)

November 1, 2018

Study Completion (Actual)

November 1, 2018

Study Registration Dates

First Submitted

June 4, 2018

First Submitted That Met QC Criteria

June 14, 2018

First Posted (Actual)

June 15, 2018

Study Record Updates

Last Update Posted (Actual)

November 27, 2018

Last Update Submitted That Met QC Criteria

November 26, 2018

Last Verified

November 1, 2018

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 380/17

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

the results of the study will be analysed. a paper will be submitted to international journal with study description including methods, examination protocol and results

IPD Sharing Time Frame

following completion of data collection

IPD Sharing Access Criteria

according to journal policy

IPD Sharing Supporting Information Type

  • Study Protocol
  • Clinical Study Report (CSR)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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