Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Multidisciplinary Health Monitoring for Esports Players

23. juni 2026 opdateret af: Yeditepe University

Evaluating the Effectiveness of a Multidisciplinary Health Monitoring and Preventive Intervention Model for Esports Players

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.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

30

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ja

Beskrivelse

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:

  • 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)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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).
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).
Ingen indgriben: 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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in core endurance (McGill Core Endurance Test Battery)
Tidsramme: Baseline and 12 weeks
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.
Baseline and 12 weeks

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in upper extremity function (DASH)
Tidsramme: Baseline and 12 weeks
Self-reported upper extremity disability measured with the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire.
Baseline and 12 weeks
Change in pain (McGill Pain Questionnaire, MPQ)
Tidsramme: Baseline and 12 weeks
Pain experience assessed with the short-form McGill Pain Questionnaire.
Baseline and 12 weeks
Change in functional exercise capacity (6-Minute Walk Test)
Tidsramme: Baseline and 12 weeks
Distance walked in 6 minutes (meters), reflecting cardiovascular/functional capacity.
Baseline and 12 weeks
Change in muscle mechanical properties (MyotonPRO)
Tidsramme: Baseline and 12 weeks
Muscle tone, stiffness, and elasticity measured with the MyotonPRO device.
Baseline and 12 weeks
Change in hand grip strength (Jamar dynamometer)
Tidsramme: Baseline and 12 weeks
Maximal grip strength measured with a Jamar hydraulic hand dynamometer.
Baseline and 12 weeks
Change in posture (PostureScreen Mobile)
Tidsramme: Baseline and 12 weeks
Postural angular deviations of head, shoulder, trunk, and hip segments assessed photogrammetrically with the PostureScreen Mobile application.
Baseline and 12 weeks
Change in Maximal inspiratory pressure (MIP)
Tidsramme: Baseline and 12 weeks
Maximal inspiratory pressure measured with the Micro RPM device.
Baseline and 12 weeks
Change in attention (d2 Test of Attention)
Tidsramme: Baseline and 12 weeks
Attention performance assessed with the d2 Test of Attention.
Baseline and 12 weeks
Change in sleep quality (Pittsburgh Sleep Quality Index, PSQI)
Tidsramme: Baseline and 12 weeks
Sleep quality measured with the Pittsburgh Sleep Quality Index.
Baseline and 12 weeks
Change in psychological status (DASS-21)
Tidsramme: Baseline and 12 weeks
Depression, anxiety, and stress levels measured with the DASS-21 scale.
Baseline and 12 weeks
Change in maximal expiratory pressure (MEP)
Tidsramme: Baseline and 12 weeks
Maximal expiratory pressure measured with the Micro RPM device.
Baseline and 12 weeks
Change in response inhibition (Go/No-Go Test)
Tidsramme: Baseline and 12 weeks
Response inhibition assessed with the Go/No-Go task.
Baseline and 12 weeks

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. september 2026

Primær færdiggørelse (Anslået)

1. december 2028

Studieafslutning (Anslået)

1. marts 2029

Datoer for studieregistrering

Først indsendt

18. juni 2026

Først indsendt, der opfyldte QC-kriterier

23. juni 2026

Først opslået (Faktiske)

24. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

24. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Muskuloskeletale smerter

3
Abonner