Effects of Oculomotor Exercises on Volleyball Players

April 17, 2021 updated by: elif yazgan, Istanbul Medipol University Hospital

Effects of Oculomotor Exercises on Balance, Dynamic Visual Acuity and Performance in Volleyball Players

The researcher aimed to investigate the effects of oculo-motor exercises on dynamic visual acuity, balance and performance of volleyball players whose performance can be improved with visual skills training.

H0: Oculo-motor exercises applied to volleyball players are effective on dynamic visual acuity, balance and performance.

H1: Oculo-motor exercises have no effect on dynamic visual acuity, balance and performance in volleyball players.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study on the Effect of Oculo-Motor Exercises on Dynamic Visual Acuity, Balance and Performance in Volleyball Players was ethically approved by the "Istanbul Medipol University Non-Invasive Ethics Committee" with file number 10840098-604.01.01-E.14171 on 16.04.2020. The study included 52 female volleyball players aged 16-26 who played participants for at least 3 years without interruption. Power analysis was performed using the 3.1.9.5 version of the G-Power program to determine the number of individuals to be included in the study. Type-1 was accepted as 0.05 and power ratio as 80%. Effect size 0.8 was taken. According to the results of the power analysis, the number of participants required to be included in the study was determined as 52.

Participants; Age, height, weight, gender, body mass index, dominant side, position played in volleyball, number of weekly training, daily training time, previous sports injuries, education status, smoking and alcohol use, accompanying illnesses were questioned. FBT and YBT were used for balance evaluations, and Nelson's Hand Reaction Test was used for reaction times. In addition, Dynamic Visual Acuity and Vertical Jumping distances were evaluated twice before and after treatment.

Participants included in the study, the control group continued their routine ball training after the evaluations, while the intervention group continued with the oculo-motor training for 4 weeks, 6 days a week, in the morning and evening, for 10 minutes, 2 times a day, in addition to normal ball training. they did the exercises. While doing the exercises, individuals were taught to focus on the purpose they held in their hands, move their head, and aim fast enough to see the image clearly. Two repetitions each week were added to the exercise numbers. Ten seconds rest between two sets and five seconds rest between movements.

Study Type

Interventional

Enrollment (Actual)

52

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

      • İstanbul, Turkey, 3434
        • Elif Aleyna Yazgan

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

16 years to 26 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Being in the age range of 16-26
  • Playing licensed volleyball for at least 3 years without interruption
  • Have normal vision and hearing

Exclusion Criteria:

  • Having a direct blow to the lower or upper extremity in the past month
  • People with musculoskeletal disorders may experience balance (forward head posture).
  • Refractive defects
  • History of ankle fracture
  • Double-sided ankle sprain
  • Vision problems
  • History of lower extremity surgery in the last 6 months

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: No intervention group
The control group continued with routine training after evaluations.
Experimental: Oculomotor exercise group
After the evaluation, the intervention group performed oculo-motor exercises for 4 weeks, 6 days a week, morning and evening, twice a day for 10 minutes, in addition to normal ball training. While doing the exercises, individuals were taught to focus on the purpose they held in their hands, move their head, and aim fast enough to see the image clearly. Two repetitions each week were added to the exercise numbers. Ten seconds rest between two sets and five seconds rest between movements.
  1. While holding the head in the middle position, holding two colored objects in both hands, looking at the object in the right hand without turning the head, counting up to 10 and looking at the object in the left hand and counting up to 10,
  2. While holding a fixed head in the middle position and holding a colored object in the right hand, following the object with the eyes while moving the right hand from right to left without turning the head and returning,
  3. With the head fixed in the middle position, with the right hand on the left, eyes are fixed on the hand-held colored object and turn the head to the right and left.
  4. The head will be fixed in the middle position, the eyes will be fixed on the colored object held in the right or left hand and the arm and the head will be turned to opposite directions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Balance
Time Frame: The evaluation will be made after 4 weeks of training.
Static balance of the individuals was evaluated by Flamingo Balance Test (FDT). A wooden stick of 50 cm length, 5 cm height and 3 cm width was used in the test. Dynamic balance changes of individuals were evaluated with YDT. In the measurement of dynamic balance with Y Balance Test (YDT), the amount of reaching out on the dominant sides of all individuals was measured.
The evaluation will be made after 4 weeks of training.
Reaction time
Time Frame: The evaluation will be made after 4 weeks of training.
Reaction time Nelson hand reaction test was used.
The evaluation will be made after 4 weeks of training.
Dynamic visual acuity
Time Frame: The evaluation will be made after 4 weeks of training.
In fact, dynamic vision is defined as the ability to detect details when there is a relative movement between the observer and the target object. It was measured by reading the numbers during neck rotation. A PowerPoint containing 10 slides, each of which randomly had 5 numbers, was used to measure dynamic vision (the size of all numbers was 12 to 20 at the center of the page). Each page had 5 numbers with the same font and each person evaluated 10 pages
The evaluation will be made after 4 weeks of training.
Vertical jump
Time Frame: The evaluation will be made after 4 weeks of training.
Vertical jump test was used.
The evaluation will be made after 4 weeks of training.

Collaborators and Investigators

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

Investigators

  • Study Director: Pınar Kaya Ciddi, İstanbul Medipol University

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, 2020

Primary Completion (Actual)

March 5, 2021

Study Completion (Actual)

April 6, 2021

Study Registration Dates

First Submitted

April 8, 2021

First Submitted That Met QC Criteria

April 17, 2021

First Posted (Actual)

April 21, 2021

Study Record Updates

Last Update Posted (Actual)

April 21, 2021

Last Update Submitted That Met QC Criteria

April 17, 2021

Last Verified

April 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • Elif Aleyna Yazgan

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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