- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05901805
Validation of the Occupational Sitting and Physical Activity Questionnaire for E-Sports Players
June 5, 2023 updated by: Nilay Arman, Istanbul University - Cerrahpasa (IUC)
Electronic sports (Esports) has become a branch that started to gain popularity in the gaming community in the early 2000s and that more and more individuals are interested in.
Esports players are often called sedentary athletes because gaming requires prolonged sedentary activity.
The aim of this study is to adapt the Occupational Sitting and Physical Activity Questionnaire to individuals playing Esports and to validate it in Turkish.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Electronic sports (Esports) has become a branch that started to gain popularity in the gaming community in the early 2000s and that more and more individuals are interested in.
Esports players are often called sedentary athletes because gaming requires prolonged sedentary activity.
Although studies have examined the physical activity levels of Esports players with questionnaires, they emphasize that the results may be more variable because they do not control for potential confounding factors such as gender, age, game type, and performance level.
Among the questionnaires used in the studies, there was no study evaluating the player-specific physical activity level.
Therefore, the aim of this study is to validate the Occupational Sitting and Physical Activity Questionnaire in individuals playing Esports.
Individuals aged 12-24, who play computer games 3-4 times a week for 2-4 hours professionally or 7-14 hours a week as an amateur, and have the ability to read and understand Turkish will be included in the study.
Individuals with severe physical limitations that prevent physical activity and individuals with cognitive impairment will be excluded from the study.
Correlation of the scale with Visual Analogue Scale (VAS), International Physical Activity Questionnaire-Short Form for construct validity, Young Internet Addiction Test-Short Form (YİBT-SF) and Buss-Perry Aggression Scale will be tested, respectively.
In order to determine the test-retest reliability of the Turkish version of the scale, individuals will be asked to fill in the scale again 7-14 days after they first filled out the scale.
Study Type
Observational
Enrollment (Estimated)
30
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
- Istanbul University-Cerrahpasa
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
Esports and amateur recreational players between the ages of 12-24 who agree to voluntarily participate in the study will be included.
Description
Inclusion Criteria:
ESports Players:
- Volunteer to participate in the study
- Age between of 12-24
- Training for 2-4 hours 3-4 times a week
- Playing e-sports for at least 1 year
- Play and be licensed as an active esports player in an official esports tournament or league
Amateur Recreational players:
- Not having an e-athlete license
- Age between of 12-24
- Playing games 7-14 hours a week
- Have an active game account in any region
Exclusion Criteria:
ESports Players:
- Having had a head injury accident within the last week
- No e-sports license
- Having a congenital disease or deformity
- Having a diagnosis of psychiatric and neurological disease
- Having a diagnosis of musculoskeletal disease
Amateur Recreational players:
- Having a systemic or congenital disease
- Having a diagnosis of neurological and psychiatric disease
- Having a disorder that affects the musculoskeletal system
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 |
|---|---|---|
|
Occupational Sitting and Physical Activity Questionnaire (OSPAQ)
Time Frame: Baseline (First assessment)
|
Occupational Sitting and Physical Activity Questionnaire; It is a short scale that records the proportion of working time spent sitting, standing, walking, and doing heavy work, and the total time worked in the last five working days.
Participants will be asked to indicate the percentage of time they spend on these activities in a day.
All percentages specified by participants for sitting, standing, walking and heavy work activities will be added up.
|
Baseline (First assessment)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Occupational Sitting and Physical Activity Questionnaire (OSPAQ)
Time Frame: Within a 7-to-14-day period after the first assessment (Second assessment)
|
Occupational Sitting and Physical Activity Questionnaire; It is a short scale that records the proportion of working time spent sitting, standing, walking, and doing heavy work, and the total time worked in the last five working days.
Participants will be asked to indicate the percentage of time they spend on these activities in a day.
All percentages specified by participants for sitting, standing, walking and heavy work activities will be added up.
|
Within a 7-to-14-day period after the first assessment (Second assessment)
|
|
International Physical Activity Questionnaire-Short Form (IPAQ-Short Form)
Time Frame: Baseline (First assessment)
|
IPAQ was developed to measure the health and physical activity levels of the society.
This global scale allows the assessment of physical activity.
The short version provides information about the time spent walking, moderate and vigorous activities, and sedentary activities.
Outcome evaluation is carried out by reporting weekly activity duration with an estimation of MET energy expenditure for each activity category.
|
Baseline (First assessment)
|
|
Visual Analogue Scale (VAS)
Time Frame: Baseline (First assessment)
|
The VAS is a pain assessment scale using a 10 cm line graded as "no pain" 0 points and "worst pain imaginable" 10 points.
|
Baseline (First assessment)
|
|
Young Internet Addiction Test-Short Form (YİBT-SF)
Time Frame: Baseline (First assessment)
|
The YİBT-SF, which measures internet addiction, consists of 12 items and is a five-point Likert scale (1=Never, 5=Very often).
|
Baseline (First assessment)
|
|
Buss-Perry Aggression Questionnaire
Time Frame: Baseline (First assessment)
|
It is an aggression assessment scale consisting of 34 items.
The situations described in the items question five sub-forms of aggression (physical aggression, verbal aggression, anger, hostility, and indirect aggression).
It is a five-point Likert-type self-rating scale.
|
Baseline (First assessment)
|
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 (Estimated)
September 1, 2023
Primary Completion (Estimated)
December 1, 2023
Study Completion (Estimated)
December 1, 2023
Study Registration Dates
First Submitted
June 5, 2023
First Submitted That Met QC Criteria
June 5, 2023
First Posted (Estimated)
June 13, 2023
Study Record Updates
Last Update Posted (Estimated)
June 13, 2023
Last Update Submitted That Met QC Criteria
June 5, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IstanbulUC2023
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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