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Not yet recruitingNCT07665333Updated Jun 24, 2026

Multidisciplinary Health Monitoring for Esports Players

An interventional study of Multidisciplinary Preventive Exercise Program in Musculoskeletal Pain, Sedentary Behavior and Diet Habit, sponsored by Yeditepe University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to male participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-24.

Sponsored by Yeditepe University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Male
01

Study summary

This study aims to develop a holistic, multidisciplinary health monitoring/screening module that evaluates the health and performance parameters of esports players, and to apply and assess the effectiveness of an individualized multidisciplinary preventive intervention program (PIP) based on the screening findings. Esports players are frequently exposed to prolonged sitting, repetitive movements, high screen time, and irregular lifestyle habits, which can lead to musculoskeletal problems, visual strain, increased cardiovascular load, sleep disturbances, and psychological effects. Comprehensive, systematic, and multidisciplinary screening models addressing these risks remain limited in the literature.

Amateur and/or professional players from the Yeditepe University Esports Club will undergo a multidimensional baseline assessment covering cardiovascular and respiratory parameters, musculoskeletal analysis, visual strain, nutritional status, cognitive function, and mental status. Participants will then be allocated to a control group or an intervention group. The intervention group will complete a 12-week individualized preventive exercise protocol in addition to their usual training, while the control group continues their usual training routine. All measurements will be repeated after 12 weeks to evaluate the effectiveness of the program.

02

Conditions studied

  • Musculoskeletal Pain
  • Sedentary Behavior
  • Diet Habit
  • Physiological Stress

Keywords

  • Esport athletes
  • Preventative intervention
  • Exercise program
03

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged 18-35 years
  • Active esports player at university or professional level
  • Regularly engaged in esports training/play for at least the past 6 months (>=3 days/week)
  • Cognitively able to understand and complete the tests and questionnaires
  • Average daily screen/gaming exposure of >=3 hours
  • Willing to participate in the assessment and exercise program and providing written informed consent

Exclusion criteria

Exclusion Criteria:

  • Serious musculoskeletal injury or surgery within the past 6 months
  • Diagnosed neurological disease (e.g., epilepsy, MS, Parkinson's)
  • Cardiovascular or respiratory disease that contraindicates exercise
  • Diagnosed serious psychiatric disorder (e.g., major depression, bipolar disorder, psychotic disorders) or being in active treatment
  • Regular medication use at a level that could affect physiological or cognitive measurements
  • Any condition that would prevent regular participation throughout the study (e.g., time constraints, lack of motivation)
04

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Multidisciplinary Preventive Exercise Program

    Participants in this arm continue their usual esports training and additionally receive a 12-week individualized multidisciplinary preventive physiotherapy and rehabilitation program. The program is delivered 2 days per week and consists of dynamic stretching/mobility exercises, strength and endurance exercises, and vestibular/visual training, integrated into gameplay (a 5-minute exercise block during the 10-minute break after each 45-minute play session).

    Behavioral: Multidisciplinary Preventive Exercise Program

  • No intervention
    Control Group

    Participants in this arm continue their usual esports training routine without any additional preventive exercise program. The same multidimensional assessments are administered at baseline and at week 12.

Interventions

  • BehavioralMultidisciplinary Preventive Exercise Program

    A 12-week individualized program delivered 2 days per week, integrated into gameplay as a 5-minute exercise block during the 10-minute break following each 45-minute play session. Three components: (1) dynamic stretching and mobility (thoracic extension, hip swings, pectoralis dynamic stretches; 2 sets x 10 reps each); (2) strength and endurance (craniocervical flexion 2x15 with 10-sec holds, plank 3x15 sec, isometric wrist extension 3x45 sec at 30% MVIC, air squats 3x12); (3) vestibular and visual training (quiet eye training 2x15, letter-tracking, and sport-specific VOR training 3x20 sec each).

05

What researchers measure

Primary outcomes

  1. Change in core endurance (McGill Core Endurance Test Battery)

    Trunk muscle endurance assessed with the McGill Core Endurance Test Battery (trunk flexor, extensor, and lateral bridge endurance times in seconds). Change from baseline to week 12 is compared between groups.

    Time frame: Baseline and 12 weeks

Secondary outcomes

  1. Change in upper extremity function (DASH)

    Self-reported upper extremity disability measured with the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire.

    Time frame: Baseline and 12 weeks

  2. Change in pain (McGill Pain Questionnaire, MPQ)

    Pain experience assessed with the short-form McGill Pain Questionnaire.

    Time frame: Baseline and 12 weeks

  3. Change in functional exercise capacity (6-Minute Walk Test)

    Distance walked in 6 minutes (meters), reflecting cardiovascular/functional capacity.

    Time frame: Baseline and 12 weeks

  4. Change in muscle mechanical properties (MyotonPRO)

    Muscle tone, stiffness, and elasticity measured with the MyotonPRO device.

    Time frame: Baseline and 12 weeks

  5. Change in hand grip strength (Jamar dynamometer)

    Maximal grip strength measured with a Jamar hydraulic hand dynamometer.

    Time frame: Baseline and 12 weeks

  6. Change in posture (PostureScreen Mobile)

    Postural angular deviations of head, shoulder, trunk, and hip segments assessed photogrammetrically with the PostureScreen Mobile application.

    Time frame: Baseline and 12 weeks

  7. Change in Maximal inspiratory pressure (MIP)

    Maximal inspiratory pressure measured with the Micro RPM device.

    Time frame: Baseline and 12 weeks

  8. Change in attention (d2 Test of Attention)

    Attention performance assessed with the d2 Test of Attention.

    Time frame: Baseline and 12 weeks

  9. Change in sleep quality (Pittsburgh Sleep Quality Index, PSQI)

    Sleep quality measured with the Pittsburgh Sleep Quality Index.

    Time frame: Baseline and 12 weeks

  10. Change in psychological status (DASS-21)

    Depression, anxiety, and stress levels measured with the DASS-21 scale.

    Time frame: Baseline and 12 weeks

  11. Change in maximal expiratory pressure (MEP)

    Maximal expiratory pressure measured with the Micro RPM device.

    Time frame: Baseline and 12 weeks

  12. Change in response inhibition (Go/No-Go Test)

    Response inhibition assessed with the Go/No-Go task.

    Time frame: Baseline and 12 weeks

06

Study locations

1 site
  • Yeditepe University Kozyatağı Hospital
    Istanbul, Turkey (Türkiye)
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07665333
Lead sponsor
Yeditepe University
Responsible party
Sponsor
First posted
Jun 24, 2026
Start date
Sep 2026 (estimated)
Primary completion
Dec 2028 (estimated)
Completion
Mar 2029 (estimated)
Last update
Jun 24, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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