Influence of Gait and Running on Foot Posture

July 17, 2023 updated by: Aurora Castro Mendez, University of Seville

Influence of Gait and Running on Foot Posture Index and Navicular Drop Modifications for Non-athletes.

Objective: To evaluate in a sample of healthy non-athlete subjects, if the foot tends to a pronated position during a period of running compared to walking, evaluated during and after one hour after performing said activity.

Design: Quasi-experimental study, experimental and control group. Setting: Subjects who attend the Podiatry Clinical Area of the University of Seville.

Participants: N=72 healthy non-athlete volunteer adults who regularly run.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Interventions: The volunteers will participate in the research on three occasions, the day of data collection, one day when they will carry out a one-hour walking period and on another occasion where they will carry out an hour of running. Changes in foot posture [FPI] or foot pronation position (navicular drop [ND]) were identified in various periods of time at the time of the initial assessment and examination (p1), after 30 minutes of walking or running ( p2), 45 minutes of walking or running (p3) and 60 minutes of walking or running (p4) of the activity elapsed.

Main outcome measures: Foot position will be measured using the Foot Posture Index (FPI) and navicular height using the navicular drop test (ND) at p1, p2, p3 and p4.

Study Type

Observational

Enrollment (Estimated)

25

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 Contact

Study Contact Backup

Study Locations

      • Sevilla, Spain, 41018
        • Recruiting
        • Aurora Castro Mendez
        • Contact:
          • aurora c mendez
          • Phone Number: 677608957

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Healthy non atletes subjects

Description

Inclusion Criteria:

The inclusion criteria are: healthy adults, of both sexes, who come to the center on the indicated date and who are professional athletes but who do practice some regular physical activity, understood as running for one hour three times a week as minimum.

-

Exclusion Criteria:

a congenital or traumatic foot deformity, wearing plantar supports, pregnancy or being in current rehabilitation treatment or serious illness.

-

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
control
healthy adults than gait over 1 hour,
the tendency to foot pronation in healthy subjects will be compared during one hour of walking versus one hour of running in subjects who usually run.
Other Names:
  • Navicular drop test
experimental
healthy adults that run over 1 hour
the tendency to foot pronation in healthy subjects will be compared during one hour of walking versus one hour of running in subjects who usually run.
Other Names:
  • Navicular drop test

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Foot posture index
Time Frame: 15 minutes

The FPI consists of 6 criteria obtained from the subject's foot where each of them gives a score from -2 to +12. Its use is simple and is scientifically validated.

The subject must be in a comfortable standing position where they support their feet as they usually do naturally. Its realization lasts approximately 2 minutes maximum for each of the feet, and after its execution an independent total value is obtained for each one of them that indicates a pronated, supinated or normal posture that goes from -12 to +12 value. .

15 minutes
navicular drop test
Time Frame: 15 minutes
to evaluate the difference between the original height of the navicular tuberosity in sitting position and in load corresponds to the drop of the scaphoids, therefore, to the descent of the internal longitudinal arch
15 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Foot posture index
Time Frame: 60 minutes

The FPI consists of 6 criteria obtained from the subject's foot where each of them gives a score from -2 to +12. Its use is simple and is scientifically validated.

The subject must be in a comfortable standing position where they support their feet as they usually do naturally. Its realization lasts approximately 2 minutes maximum for each of the feet, and after its execution an independent total value is obtained for each one of them that indicates a pronated, supinated or normal posture that goes from -12 to +12 value. .

60 minutes
Navicular drop test
Time Frame: 60 minutes
o evaluate the difference between the original height of the navicular tuberosity in sitting position and in load corresponds to the drop of the scaphoids, therefore, to the descent of the internal longitudinal arch
60 minutes

Collaborators and Investigators

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

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 20, 2023

Primary Completion (Actual)

June 20, 2023

Study Completion (Estimated)

July 25, 2023

Study Registration Dates

First Submitted

June 28, 2023

First Submitted That Met QC Criteria

July 7, 2023

First Posted (Actual)

July 17, 2023

Study Record Updates

Last Update Posted (Actual)

July 19, 2023

Last Update Submitted That Met QC Criteria

July 17, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 0973-N-20

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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