The Effect of Posture and Scapular Position on Performance Parameters in E-sport Players

February 26, 2025 updated by: Ömer Bayrak

The research aims to examine how shoulder proprioception, scapular position, physical activity levels and posture influence key performance factors such as visual reaction time, audiotory reaction time and hand-eye coordination.

Various digital tools and tests will be utilized for assessment, including reaction time tests and hand-eye coordination evaluations conducted through HumanBenchmark and Audioreactiontime websites respectively, as well as posture analysis via mobile applications. Shoulder proprioception will be measured at specific flexion angles using a smartphone-based inclinometer, while scapular dyskinesis will be assessed through the lateral scapular sliding test. Additionally, participants' physical activity levels, assessed via the International Physical Activity Questionnaire (IPAQ), will be analyzed to determine potential correlations.

Study Overview

Status

Completed

Conditions

Detailed Description

E-sport is a competitive sport based on video games played professionally and multiplayer. To perform successfully in e-sport, high coordination and good reaction speed are essential. Studies indicate that prolonged inactivity and lack of physical activity in front of the computer can lead to weakening of motor skills and postural disorders. Additionally, abnormal positioning and movement of the scapula may reflect changes in the activity of surrounding muscles, potentially disrupting the coordinated movement with the humerus and possibly affect shoulder proprioception.

Based on this information, the investigators hypothesize that scapular dyskinesis and postural disorders in e-sport players affect their performance. The aim of our study is to investigate the impact of scapular position and posture on performance parameters, including hand-eye coordination, reaction time, shoulder proprioception, and physical activity among e-sport players.

For the assessment of visual reaction time, will be measured using the test on available on "humanbenchmark.com" will be used. Auditory reaction time will be measured using the test available on "playback.fm." Hand-eye coordination will be evaluated through the "Aim Reaction" test. Posture assessment will be conducted using the mobile application "PostureScreen."

Shoulder joint position sense will be assessed with the smartphone application "Clinometer" at 55°, 90°, and 125° shoulder flexion angles. Scapular dyskinesis will be evaluated using the lateral scapular sliding test at three different shoulder angles with a caliper.

The physical activity levels of the e-sport players will be determined using the International Physical Activity Questionnaire (IPAQ).

Study Type

Observational

Enrollment (Actual)

27

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

  • Turkey
    • Eyüpsultan
      • İstanbul, Eyüpsultan, Turkey, 34030
        • Haliç 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

Yes

Sampling Method

Non-Probability Sample

Study Population

E-sport Players in FUT E-sport Teams

Description

Inclusion Criteria:

Individuals aged between 18 and 25 years. Professional engagement in PC or mobile e-sports for at least 6 hours per week continuously for the last six months.

PC professional e-sports players compete at a high level within a team, participating in competitive PC gaming.

Mobile professional e-sports players compete at a high level within a team, participating in competitive mobile gaming.

Control group: Individuals aged 18-25 years who played video games for less than 6 hours per week.

Exclusion Criteria For All Groups:

Any neurological, visual, or auditory impairment. History of upper extremity surgery. Use of medications known for their stimulant properties. Conditions that could interfere with test performance.

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
Mobile E-sport Players
Mobile professional e-sports players compete at a high level within a team, participating in competitive mobile gaming.
PC E-sport Players
PC professional e-sports players compete at a high level within a team, participating in competitive PC gaming.
Control group
Individuals aged 18-25 years who played video games for less than 6 hours per week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The International Physical Activity Questionnaire (IPAQ)
Time Frame: Baseline

The International Physical Activity Questionnaire (IPAQ) short form will assess e-sport players' physical activity levels. This validated questionnaire consists of seven items measuring time spent on walking, moderate, and vigorous activities, with energy expenditure expressed as MET minutes per week. The total score is calculated by summing the duration (minutes) and frequency (days) of each activity, while sedentary time is recorded separately. Only activities lasting at least 10 consecutive minutes are included.

Scores are calculated as "MET minutes/week" by multiplying duration, frequency, and MET values: walking (3.3 METs), moderate (4 METs), and vigorous activity (8 METs). Physical activity levels are classified as:

Physically inactive: <600 MET-min/week Low activity: 600-3000 MET-min/week Adequate activity: >3000 MET-min/week The Turkish IPAQ forms are validated for reliability.
Baseline
Auditory Reaction Time Test
Time Frame: Baseline
Auditory reaction time will be assessed using the playback.fm test (https://playback.fm/audio-reaction-time). Participants will press the "spacebar" on the keyboard upon hearing a sound. The test consists of five trials, and the average reaction time (ms) will be calculated from the recorded results.
Baseline
Visual Reaction Time Test
Time Frame: Baseline
Visual reaction time will be assessed using the "Reaction Time" test on the Human Benchmark website (https://humanbenchmark.com/tests/reactiontime). Participants will press a button as soon as the screen turns green. The test consists of five trials, and the average reaction time (ms) will be calculated from the recorded results.
Baseline
Hand-Eye Coordination
Time Frame: Baseline
The hand-eye coordination assessment is performed with the "Aim Reaction" test. The test is called "Aim Trainer" and is available on the website (https://humanbenchmark.com/tests/aim). At the beginning of the test, the participant tries to hit 30 targets on the screen as quickly and accurately as possible. After completing the test, the mean time to hit each target is displayed in milliseconds (ms)
Baseline
Scapular Dyskinesis Assessment
Time Frame: Baseline

Scapular dyskinesis will be assessed using a digital caliper based on the Kibler method, which has shown moderate to high reliability. The distance between the inferior angle of the scapula and the spinous process of the 7th thoracic vertebra (scapular distance) will be measured in centimeters (cm) across three positions:

Arms at sides (0° abduction) Hands on iliac crest (45° abduction) 90° shoulder abduction with internal rotation Measurements are taken with the caliper's distal arm at the scapula's inferior angle and the proximal arm at the spinous process. Participants remain relaxed and focus on a fixed point. A ≥1.5 cm difference between scapulae indicates dyskinesis. The mean scapular distance is recorded for analysis.
Baseline
Posture Assessment
Time Frame: Baseline

Posture will be assessed using the mobile application "PostureScreen," employing the photographic method. The application calculates posture based on reference points marked on the anterior, posterior, and lateral aspects of a photograph. These reference points, along with athlete and assessor positioning, follow the guidelines outlined in the 2018 study by Iacob et al. The method is validated and reliable, with ICC scores ranging from 0.71 to 0.99.

The application measures anterior and posterior shifts and tilts of the head, shoulders, chest, and hips, as well as lateral shifts and tilts of the head, shoulders, and hips. The total shift and tilt values are calculated as the sum of these measurements. These values will be used to generate a report detailing the participant's posture and its deviation from normal posture.
Baseline
Shoulder Joint Position Sense
Time Frame: Baseline

Shoulder joint position sense will be assessed using the "Clinometer" smartphone application (ICC = 0.98). The assessment follows a 5-minute warm-up with calisthenic exercises for the glenohumeral and scapulothoracic joints.

The participant will be tested in shoulder flexion positions of 55°, 90°, and 125°. The smartphone is fixed between the shoulder and elbow to minimize deviations. The 55° position is first practiced with eyes open, then with eyes closed, holding for 10 seconds before returning to the starting position. The participant then identifies the target angle (55°) with eyes closed, responding with "OK" once reached. This process is repeated six times with 5-second rests between trials. Deviations from the target angle are recorded as absolute errors. The same procedure is followed for 90° and 125° flexion, for both arms.
Baseline

Collaborators and Investigators

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

Sponsor

Ömer Bayrak

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.

General Publications

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)

October 1, 2024

Study Completion (Actual)

November 1, 2024

Study Registration Dates

First Submitted

February 21, 2025

First Submitted That Met QC Criteria

February 21, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 26, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HUOBayrak

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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