Investigation of University Level Volleyball Players in Terms of Ankle Functions and Postural Control Variables

February 14, 2023 updated by: Aysem Ecem Ozdemir, Istanbul Gelisim University

In this study, it is aimed to evaluate different ankle functions and postural control variables in university level volleyball players and students with stable ankles and to examine the results obtained. In this way, we aim to contribute to the physiotherapy and rehabilitation literature and clinical studies of physiotherapists who are interested in athlete health.

The hypothesis set in this study is:

H0: There is no difference between ankle functions and postural control variables of volleyball players and healthy controls.

H1: There is a difference between ankle functions and postural control variables of volleyball players and healthy controls.

Study Overview

Status

Completed

Detailed Description

There are studies proving that athletes with poor postural control have a higher risk of injury to the ankle and knee regions than those with normal. Balanced stance and effective postural control in activities involving ball contact during the game are the basic skills of volleyball. The ankle is a joint that needs to be evaluated frequently and its functions should be improved both in order to improve postural control ability and to prevent possible injuries. It has been proven in studies that the capacity shown in different functional parameters such as joint range of motion, strength and proprioception and balance both reduces the risk of injury and positively reflects on the performance parameters of the athlete. It will be useful to evaluate and examine the ankle functions and postural controls that change as a result of the training and exercises performed by the athletes, unlike healthy individuals who are not athletes, in order to understand the abilities developed specifically for the sport.

The study will be carried out in Yeditepe University Physiotherapy and Rehabilitation Graduate Laboratory. Female individuals aged 18-25 years, with stable ankles will be included in the study as a sample. The study will consist of two groups. The first group will include volleyball players playing in university teams, and healthy university students meeting the same criteria in the control group. The sample size of the study was calculated using the GPower program as type 1 error value= 0.05, power = 0.90, effect size (f value) calculated from the reference article and total of 40 subjects for the independent sample t-test.

The Cumberland Ankle Instability Tool will be used to select suitable participants for the study. Only ankles considered stable according to the questionnaire will be included in this study. First, static balance will be evaluated with the PK Prokin 252 system during the silent stand for postural control assessment. Then, different ankle functions of the people who will participate in the study will be evaluated. The measurement of the range of motion of the ankle will be evaluated with the help of a goniometer. Different degrees of position sense of the ankle joint will be evaluated with the aid of a goniometer and the sense of vibration will be evaluated with a tuning fork. Muscle strength will be measured with the help of a manual dynamometer during the movements of the muscles around the ankle. In addition, the participants who volunteered to participate in the study before the tests will be given a Voluntary Consent Form and a Demographic Information Form. Participants will be given rest periods between each test. Evaluation time will be 45 minutes for each participant. Participants will not be followed up after the assessments.

Study Type

Observational

Enrollment (Actual)

40

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

      • Istanbul, Turkey, 34000
        • Yeditepe Üniversitesi

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

Female

Sampling Method

Non-Probability Sample

Study Population

The study was carried out with female individuals aged 18-25 who have stable ankles and have not had an ankle injury in the last 1 year. The study includes volleyball players playing in university teams and healthy university students who meet the same criteria.

Description

Inclusion Criteria:

  • Female gender,
  • Being between the ages of 18-25,
  • Having a score of ≥24 on the Cumberland Ankle Instability Questionnaire,
  • Volunteering for the study.

Exclusion Criteria:

  • Presence of neuromuscular system disease,
  • Presence of vestibular or visual problems,
  • Presence of acute or chronic pain,
  • An ankle injury in the last year,
  • For the control group, regular participation in sports activities or physical activity for more than 150 minutes, 5 days a week.

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

  • Observational Models: Case-Control
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Volleyball Group
Female Volleyball players who are currently playing in a university team and who are meeting the inclusion criteria.
Control Group
Female university students who are meeting the inclusion criteria.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postural control
Time Frame: Baseline
Postural control is evaluated according to the results of the static stability test performed on the PK Prokin 252 balance device with proven reliability. Postural control outcome is measured by the findings of the Prokin System, wich are: Average center of gravity on the X-axis (mm), Average Y-axis center of gravity (mm), Forward-backward standard deviation (mm), Medial-lateral standard deviation (mm) variables.
Baseline
Ankle Joint Range of Motion
Time Frame: Baseline
Range of motion assessment is made using a goniometer. Dorsiflexion and plantarflexion in the tibiotalar joint, and eversion and inversion in the subtalar joint is evaluated both actively and passivley. These evaluations will be repeated 3 times and their averages will be recorded.
Baseline
Ankle Joint Proprioception
Time Frame: Baseline
The assessment is made by a goniometer. First the referance degree is passively tought and then while eyes are closed, the person tries to reach the referance degree. The movements starts from 145 degrees of plantar flexion to the degrees of 105, 120, 130 and 140.
Baseline
Vibration Sense
Time Frame: Baseline
Vibration evaluation is made with the help of tuning fork (128 Hz). The eyes are closed throughout the application. Reference points are the big toe, fifth toe, and medial malleolus. The person is instructed to say when the feeling of vibration ends. A timer was used to count the time.
Baseline
Ankle Joint Muscle Strength
Time Frame: Baseline
The maximum isometric strength of the ankle is evaluated with the manual dynamometer measurement, the validity and reliability of which has been proven. JTECH Commander Powertrack Manual Dynamometer was used for measurements. Dorsiflexion, plantar flexion, eversion and inversion movements are assessed.
Baseline

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cumberland Ankle Instability Tool
Time Frame: Baseline
The tool is used to to understand if the ankle is stable or unstable. The scale consists of nine questions about ankle joint functions and whether there is pain in different activities and a total of 30 points. Functional instability increases with low scores from the questionnaire. The cutoff point for the stable ankle is ≥24.
Baseline

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)

August 25, 2022

Primary Completion (Actual)

January 24, 2023

Study Completion (Actual)

February 8, 2023

Study Registration Dates

First Submitted

June 9, 2022

First Submitted That Met QC Criteria

June 9, 2022

First Posted (Actual)

June 13, 2022

Study Record Updates

Last Update Posted (Actual)

February 15, 2023

Last Update Submitted That Met QC Criteria

February 14, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

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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