Relationship Between Foot-ankle Characteristics and Lumbopelvic Control, Balance and Physical Performance

November 30, 2017 updated by: Caner Karartı, Hacettepe University

Investigation of the Relationship Between Foot-ankle Characteristics and Lumbopelvic Control, Balance and Physical Performance in Healthy Young Adults.

It has been shown that foot and ankle postural disorders can alter the biomechanic of lower extremity and pelvis. This situation can affects balance, postural control and phsical performance of individual adversely. However, it is unknown whether the muscles that control lumbopelvic are affected or not affected. The aim of this study is to investigate the relationship between foot-ankle characteristics and lumbopelvic control, balance and physical performance in healthy young adults.

Study Overview

Detailed Description

A healthy load distribution at the foot depends on the ability of the foot to fulfill both the task of stabilization and mobilization. Studies related foot movement disorders usually focus on subtalar joint. The reason for this is that subtalar joint transmits the rotations which in leg to the foot. One of the deformities affecting the foot and subtalar joint is pes planus. Kosashvili et al. have shown that grade 2 and 3 pes planus can affect the lower limb biomechanical alignment, resulting in an increase in perceived pain associated with the knee, hip and pelvic region. Problems related to foot and ankle can affect the balance of individuals as well as affect the pelvic region. Sung et al. have shown that the postural stability and balance of individuals with pes planus are worse than those without pes planus. Studies showing that foot-ankle postural disorders negatively affect physical fitness and motor performance of individuals are also present. Akaras et al. have stated that the increase in pronation in the hindfoot affects individuals' leap and agility performance negatively. It has shown that leg-related problems can affect upper. However, there is no objective study of ultrasonographic imaging of core muscles in foot-ankle problems. The aim of this study is to investigate the relationship between foot-ankle characteristics and lumbopelvic control, balance and physical performance in healthy young adults.

Study Type

Observational

Enrollment (Actual)

64

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

      • Ankara, Turkey
        • Hacettepe University

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

18 years to 25 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

64 healthy young adults

Description

Inclusion Criteria:

  • Volunteering to participate.
  • Be between the ages of 18 and 25
  • Being a normal weighted individual with a body mass index from 18.5 to 24.9

Exclusion Criteria:

  • Presence of any systemic, locomotive or foot related problem
  • Undergone any surgical operation related to the foot
  • To have loss of sense, diabetic or peripheral neuropathy
  • The presence of any problem with the spine (back pain, scoliosis, past surgeons)
  • Presence of any neurological problem

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
INVESTIGATION OF THE RELATIONSHIP BETWEEN FOOT-ANKLE CHARACTERISTICS AND LUMBOPELVIC CONTROL, BALANCE AND PHYSICAL PERFORMANCE IN HEALTHY YOUNG ADULTS
Time Frame: 2 months
Adverse changes in foot-ankle characteristics in healthy young adults affect lumbopelvic control, balance and phsical performance adversely.
2 months

Collaborators and Investigators

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

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.

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)

November 20, 2017

Primary Completion (ANTICIPATED)

December 20, 2017

Study Completion (ANTICIPATED)

January 20, 2018

Study Registration Dates

First Submitted

November 27, 2017

First Submitted That Met QC Criteria

November 27, 2017

First Posted (ACTUAL)

December 2, 2017

Study Record Updates

Last Update Posted (ACTUAL)

December 4, 2017

Last Update Submitted That Met QC Criteria

November 30, 2017

Last Verified

November 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2017200

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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