Foot Positions Affect Basketball Players With Flatfoot

April 28, 2025 updated by: Ayman Mohamed, Beni-Suef University

Effect of Various Initial Foot Positions on Proprioception, Balance, Jump, and Electromyographical Muscle Activity in Basketball Players With Flatfoot and Chronic Ankle Instability: A Cross-sectional Study

This study investigated the effect of various initial foot positions on knee and ankle proprioception, balance, dynamic balance, vertical jump, and electromyographical muscle activity in basketball players with FF.

Study Overview

Status

Completed

Detailed Description

Objective: To investigate the effect of various initial foot positions on knee and ankle proprioception, balance, dynamic balance, vertical jump, and electromyographical muscle activity in basketball players with FF.

Methods: Eighty-four basketball players with chronic ankle instability were distributed to three groups (28 with flexible FF, 28 with rigid FF, and 28 without FF). The outcome measures will include static and dynamic balance, knee and ankle proprioception, vertical jump, and electromyography (EMG) of ankle muscles (including gastrocnemius (GE), soleus (SOL), tibialis anterior (TA), and peroneus longus (PL) muscles)

Study Type

Observational

Enrollment (Actual)

84

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

    • Beni Suef
      • Banī Suwayf, Beni Suef, Egypt
        • Nahda 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

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Basketball players with chronic ankle instability

Description

Inclusion Criteria:

  • The presence of flatfoot in the dominant leg.
  • The presence of chonic ankle instability

Exclusion Criteria:

  • The exclusion criteria were the existence of limited hallux dorsiflexion
  • previous hip, pelvis, knee, or foot surgeries within the last year; obesity or pregnancy; leg-length discrepancies;
  • Had any vestibular disorder neurological disorder, brain concussion within the last 3 months that may cause balance impairment; or administering any drugs that could disturb alertness or balance

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
flexible FF
28 basketball player with flexible flatfoot and chronic ankle instability
Rigid FF
28 basketball player with rigid flatfoot and chronic ankle instability
Control
28 basketball player without flatfoot but chronic ankle instability

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee proprioception with repositioning error test
Time Frame: 3 months
The knee proprioception will be measured using the repositioning error test on the dominant leg to measure the absolute angular error. This test will assess the ability of the participant to reproduce a previously performed position (45 and 15 degrees of knee flexion).
3 months
Ankle proprioception with angular error measurement test
Time Frame: 3 months
This test will assess the ability of the participant to reproduce previously performed ankle positions (15° dorsiflexion and 15° plantar flexion.)
3 months
Static balance with The Y-Balance test
Time Frame: 3 months
The Y-Balance test will be used to evaluate static balance 27. The test will assess the ability of the participant to maintain balance while reaching as far as possible in all three directions (anterior (A), posteromedial (PM), and posterolateral (PL) directions).
3 months
Dynamic balance with Biodex Balance device
Time Frame: 3 months
In this study, dynamic balance will be measured by the Biodex Balance System (Biodex 945-302, Biodex Medical Systems Inc., New York, USA). The Biodex Balance System has been demonstrated to be a reliable and validated instrument to assess dynamic balance. The biodex will assess the anteroposterior and lateral stability.
3 months
Vertical jump height with vertical jump tester
Time Frame: 3 months
A vertical jump tester (Sports Imports, Columbus, OH)32 will be utilized to evaluate the vertical jump height in cm of each participant. The achieved height distance in cm in each step will be recorded, and the maximum height will be used in the statistical analysis.
3 months
Electromyographical activity (EMG) during one-leg standing
Time Frame: 3 months
A wireless surface EMG system will record electromyographical signals (EMG) of ankle muscles, including gastrocnemius (GE), soleus (SOL), tibialis anterior (TA), and peroneus longus (PL) muscles.
3 months

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)

September 1, 2023

Primary Completion (Actual)

April 30, 2024

Study Completion (Actual)

April 30, 2024

Study Registration Dates

First Submitted

April 15, 2025

First Submitted That Met QC Criteria

April 28, 2025

First Posted (Actual)

April 29, 2025

Study Record Updates

Last Update Posted (Actual)

April 29, 2025

Last Update Submitted That Met QC Criteria

April 28, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

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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