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Effects of Virtual Reality-Based Optokinetic Stimulation Added to Neuromuscular Training in Basketball Players

31 octobre 2026 mis à jour par: Büşra Tamgüç, Bahçeşehir University

Comparison of the Effects of Optokinetic Stimulation Added to a Neuromuscular Training Program on Jump-Landing Biomechanics, Visual Dependence, and Reactive Transfer Performance

This study will investigate whether adding virtual reality-based optokinetic stimulation to neuromuscular training improves jump-landing movements, balance, and performance during a visually cued movement task in basketball players. Optokinetic stimulation involves watching moving visual patterns through a virtual reality headset. Neuromuscular training includes strength, balance, and jumping and landing exercises.

Forty-two licensed basketball players aged 16-35 years will be randomly assigned to one of three groups: usual team training alone (control group), neuromuscular training in addition to usual team training, or virtual reality-based optokinetic stimulation followed by neuromuscular training in addition to usual team training. The additional training will be provided three times per week for six weeks.

Assessments will be performed before and after the six-week program. The main outcome will be the maximum amount of knee bending during landing. Other assessments will examine landing forces, lower-limb movements, body movement, standing balance, and reliance on vision for balance. At the end of the program, participants will also complete a jump-landing task in response to colored lights to assess whether movement strategies are maintained under additional cognitive demands.

Aperçu de l'étude

Description détaillée

Basketball involves repeated jumping, landing, and rapid changes in movement. These activities require coordination of visual, vestibular, and somatosensory information. Neuromuscular training may improve movement control, while the additional contribution of virtual reality-based optokinetic stimulation to landing biomechanics and sensory integration will be investigated in this study.

This prospective, three-arm, parallel-group, randomized controlled trial will compare usual team training, additional neuromuscular training, and virtual reality-based optokinetic stimulation combined with the same neuromuscular training program. All participants will continue their usual team training throughout the study.

The neuromuscular training program will progressively incorporate strength, balance, proximal control, and plyometric exercises. In the combined intervention group, optokinetic stimulation will be delivered immediately before each neuromuscular training session using a virtual reality headset. Participants will visually track moving targets while keeping their head and trunk as still as possible. Visual stimulus speed, exposure duration, and postural difficulty will increase progressively over six weeks. Symptoms associated with virtual reality exposure will be monitored throughout the intervention.

Standardized drop vertical jump assessments will be performed using a force platform and an inertial motion capture system. Peak knee flexion angle during the landing deceleration phase will be the primary outcome. Additional measurements will characterize landing kinetics, lower-limb kinematics, center-of-mass movement, and tibial acceleration.

Standing balance will be assessed in tandem stance with eyes open and eyes closed. Center-of-pressure measurements and eyes-closed-to-eyes-open ratios will be used to characterize postural stability and visual dependence.

At the six-week assessment only, a reactive transfer task will require participants to perform the drop vertical jump in response to a predetermined target color and withhold movement in response to other colors. Biomechanical measurements from this task will be compared with those from the standard task to examine the maintenance of movement strategies under additional cognitive demands.

Type d'étude

Interventionnel

Inscription (Estimé)

42

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

      • Istanbul, Turquie (Türkiye), 34022
        • Bahcesehir University, Faculty of Engineering and Natural Sciences, Biomedical Engineering Motion Analysis Laboratory
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

16 ans à 35 ans (Enfant, Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

- Aged 16-35 years.

Body mass index of 18.5-25 kg/m².

Landing Error Scoring System (LESS) score of at least 6.

A licensed basketball player at a club actively competing at the second-league level.

At least three years of regular basketball playing and training experience.

Participation in regular basketball training at least three days per week, with each session lasting at least one hour.

A System Usability Scale (SUS) classification of A+ for the virtual reality system, corresponding to the 96th-100th percentile range.

No trunk or lower-extremity injury within the previous six months.

Willingness to provide written informed consent. For participants younger than 18 years, parental or legal guardian consent and participant assent will also be obtained.

Exclusion Criteria:

  • More than two weeks away from sport due to a lower-extremity injury within the previous six months.

A history of lower-extremity fracture, dislocation, or surgery resulting in functional limitations.

A congenital or acquired musculoskeletal abnormality that may affect lower-extremity biomechanics.

Inability to perform the study tasks safely because of a visual, auditory, vestibular, or neurological disorder.

A history of migraine, epilepsy, severe motion sickness, or concussion within the previous six months.

Participation in vestibular rehabilitation or a structured neuromuscular injury-prevention program within the previous six months.

Cybersickness symptoms severe enough to prevent tolerance of the virtual reality intervention.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Aucune intervention: Control Group

Participants will continue their usual basketball team training for six weeks. No additional neuromuscular training or virtual reality-based optokinetic stimulation will be provided as part of the study.

Comparateur actif: Neuromuscular Training Group

Participants will continue their usual basketball team training and additionally receive supervised neuromuscular training three times per week for six weeks, totaling 18 sessions. Each session will last approximately 25-30 minutes and include progressively advanced strength, balance, proximal control, and plyometric exercises targeting jump-landing mechanics.

Supervised neuromuscular training will be delivered three times per week for six weeks (18 sessions), in addition to usual basketball team training. Each session will last approximately 25-30 minutes and include strength, balance, proximal control, and plyometric exercises. Exercises will progress from bilateral squats, walking lunges, single-leg balance, and drop landings to single-leg squats, drop jumps, single-leg countermovement jumps, and single-leg standing long jumps. Exercises will be performed in 3-4 sets, with 60-90 seconds of rest between sets. Exercise difficulty and repetitions will progress according to the weekly protocol.

Autres noms:
  • NMT
Expérimental: VR-Based Optokinetic Stimulation Group

Participants will continue their usual basketball team training and receive the same supervised neuromuscular training program as the active comparator group, three times per week for six weeks, totaling 18 sessions. Immediately before each neuromuscular training session, participants will receive virtual reality-based optokinetic stimulation. Visual stimulus speed, exposure duration, and postural difficulty will increase progressively over the six-week intervention.

Supervised neuromuscular training will be delivered three times per week for six weeks (18 sessions), in addition to usual basketball team training. Each session will last approximately 25-30 minutes and include strength, balance, proximal control, and plyometric exercises. Exercises will progress from bilateral squats, walking lunges, single-leg balance, and drop landings to single-leg squats, drop jumps, single-leg countermovement jumps, and single-leg standing long jumps. Exercises will be performed in 3-4 sets, with 60-90 seconds of rest between sets. Exercise difficulty and repetitions will progress according to the weekly protocol.

Autres noms:
  • NMT

Optokinetic stimulation will be delivered using a Meta Quest 3S headset and custom Unity software immediately before neuromuscular training, three times per week for six weeks. Participants will track moving balloons with their eyes while keeping their head and trunk as still as possible. Weekly progression will be: week 1, seated, 20 degrees/s, 3 x 30 s; week 2, standing with feet together, 20 degrees/s, 3 x 60 s; week 3, semi-tandem stance, 30 degrees/s, 3 x 90 s; week 4, tandem stance, 40 degrees/s, 3 x 120 s; week 5, tandem stance, 50 degrees/s, 3 x 150 s; week 6, tandem stance, 60 degrees/s, 3 x 180 s. Clockwise and counterclockwise motion will be presented for equal durations. Background rotation speed will be twice the balloon speed. Symptoms will be monitored using the Simulator Sickness Questionnaire, with exposure adjusted according to tolerance.

Autres noms:
  • VR-OKS

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in Peak Knee Flexion Angle During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak knee flexion angle of the dominant limb will be measured in degrees using the Xsens MVN Awinda inertial motion capture system during a standardized drop vertical jump from a 30-cm box. The peak angle will be identified during the landing deceleration phase, from initial ground contact to maximum knee flexion. Initial contact will be determined using synchronized force-platform data. The dominant limb will be defined as the preferred leg for kicking a ball. Three successful trials will be recorded at each assessment. Change from baseline to the end of the six-week intervention will be evaluated.

Baseline and immediately after the six-week intervention

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in Peak Vertical Ground Reaction Force During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak vertical ground reaction force will be measured using a Bertec force platform sampling at 1000 Hz during the standardized drop vertical jump. Initial contact will be defined as the first instant at which filtered vertical ground reaction force exceeds 10 N. Peak force will be identified as the maximum vertical ground reaction force within the first 0.20 seconds after initial contact and normalized to body weight, expressed in multiples of body weight. Three successful trials will be recorded at each assessment. Change from baseline to the end of the six-week intervention will be evaluated.

Baseline and immediately after the six-week intervention
Change in Time to Peak Vertical Ground Reaction Force During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

The time interval between initial ground contact and peak vertical ground reaction force will be measured in seconds using a Bertec force platform sampling at 1000 Hz during the standardized drop vertical jump. Initial contact will be defined as the first instant at which filtered vertical ground reaction force exceeds 10 N. Peak vertical ground reaction force will be identified within the first 0.20 seconds after initial contact. Three successful trials will be recorded at each assessment. Change from baseline to the end of the six-week intervention will be evaluated.

Baseline and immediately after the six-week intervention
Change in Landing Load Absorption Duration During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Landing load absorption duration will be measured in seconds as the time interval between peak vertical ground reaction force and maximum knee flexion of the dominant limb during the standardized drop vertical jump. Peak vertical ground reaction force will be identified within the first 0.20 seconds after initial contact using a Bertec force platform. Maximum knee flexion will be identified using synchronized Xsens MVN Awinda motion capture data. The dominant limb will be defined as the preferred leg for kicking a ball. Three successful trials will be recorded at each assessment. Change from baseline to the end of the six-week intervention will be evaluated.

Baseline and immediately after the six-week intervention
Change in Hip Flexion Range of Motion During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Hip flexion range of motion will be measured in degrees using the Xsens MVN Awinda system, from initial ground contact to the instant of maximum dominant-knee flexion during the standardized drop vertical jump. Bilateral measurements will be calculated within the same analysis window.

Baseline and immediately after the six-week intervention
Change in Knee Flexion Range of Motion During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Knee flexion range of motion will be measured in degrees using the Xsens MVN Awinda system, from initial ground contact to the instant of maximum dominant-knee flexion during the standardized drop vertical jump. Bilateral measurements will be calculated within the same analysis window.

Baseline and immediately after the six-week intervention
Change in Ankle Dorsiflexion Range of Motion During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Ankle dorsiflexion range of motion will be measured in degrees using the Xsens MVN Awinda system, from initial ground contact to the instant of maximum dominant-knee flexion during the standardized drop vertical jump. Bilateral measurements will be calculated within the same analysis window.

Baseline and immediately after the six-week intervention
Change in Time to Peak Knee Flexion During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

The interval from initial ground contact to maximum knee flexion of the dominant limb will be measured in seconds using synchronized Bertec force-platform and Xsens MVN Awinda data during the standardized drop vertical jump.

Baseline and immediately after the six-week intervention
Change in Peak Knee Valgus Angle During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak dominant-knee valgus angle will be measured in degrees using the Xsens MVN Awinda system during the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Valgus will be defined as the maximum positive value of the dominant-knee abduction/adduction angle.

Baseline and immediately after the six-week intervention
Change in Peak Resultant Tibial Acceleration During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak resultant tibial acceleration will be calculated from the three-axis free-acceleration signals of the lower-leg sensors of the Xsens MVN Awinda system during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Acceleration will be expressed in meters per second squared.

Baseline and immediately after the six-week intervention
Change in Romberg Sway Area Ratio
Délai: Baseline and immediately after the six-week intervention

Visual dependence will be assessed using the ratio of eyes-closed to eyes-open center-of-pressure sway area measured with a Bertec force platform during tandem stance. Two 30-second trials will be performed under each condition. The ratio is dimensionless, with higher values indicating greater reliance on vision for postural control.

Baseline and immediately after the six-week intervention
Change in Romberg Sway Velocity Ratio
Délai: Baseline and immediately after the six-week intervention

Visual dependence will be assessed using the ratio of eyes-closed to eyes-open mean center-of-pressure velocity measured with a Bertec force platform during tandem stance. Two 30-second trials will be performed under each condition. The ratio is dimensionless, with higher values indicating greater reliance on vision for postural control.

Baseline and immediately after the six-week intervention
Change in Center-of-Pressure Sway Area During Tandem Stance
Délai: Baseline and immediately after the six-week intervention

Center-of-pressure sway area will be measured using a Bertec force platform during tandem stance with eyes open and eyes closed. Two 30-second trials will be performed under each condition. Results will be reported separately for each visual condition in square centimeters.

Baseline and immediately after the six-week intervention
Change in Center-of-Pressure Total Path Length During Tandem Stance
Délai: Baseline and immediately after the six-week intervention

Total center-of-pressure path length will be measured using a Bertec force platform during tandem stance with eyes open and eyes closed. Two 30-second trials will be performed under each condition. Results will be reported separately for each visual condition in centimeters.

Baseline and immediately after the six-week intervention
Change in Mean Center-of-Pressure Velocity During Tandem Stance
Délai: Baseline and immediately after the six-week intervention

Mean center-of-pressure velocity will be measured using a Bertec force platform during tandem stance with eyes open and eyes closed. Two 30-second trials will be performed under each condition. Results will be reported separately for each visual condition in centimeters per second.

Baseline and immediately after the six-week intervention
Change in Peak Anterior-Posterior Center-of-Mass Velocity During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak anterior-posterior center-of-mass velocity will be obtained from Xsens MVN Awinda data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Velocity will be expressed in meters per second.

Baseline and immediately after the six-week intervention
Change in Peak Medial-Lateral Center-of-Mass Velocity During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak medial-lateral center-of-mass velocity will be obtained from Xsens MVN Awinda data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Velocity will be expressed in meters per second.

Baseline and immediately after the six-week intervention
Change in Peak Vertical Center-of-Mass Velocity During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak vertical center-of-mass velocity will be obtained from Xsens MVN Awinda data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Velocity will be expressed in meters per second.

Baseline and immediately after the six-week intervention
Change in Peak Anterior-Posterior Center-of-Mass Acceleration During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak anterior-posterior center-of-mass acceleration will be obtained from Xsens MVN Awinda data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Acceleration will be expressed in meters per second squared.

Baseline and immediately after the six-week intervention
Change in Peak Medial-Lateral Center-of-Mass Acceleration During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak medial-lateral center-of-mass acceleration will be obtained from Xsens MVN Awinda data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Acceleration will be expressed in meters per second squared.

Baseline and immediately after the six-week intervention
Change in Peak Vertical Center-of-Mass Acceleration During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Peak vertical center-of-mass acceleration will be obtained from Xsens MVN Awinda data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Acceleration will be expressed in meters per second squared.

Baseline and immediately after the six-week intervention
Change in Anterior-Posterior Center-of-Mass Displacement During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Anterior-posterior center-of-mass displacement will be calculated from Xsens MVN Awinda position data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Displacement will be expressed in meters.

Baseline and immediately after the six-week intervention
Change in Medial-Lateral Center-of-Mass Displacement During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Medial-lateral center-of-mass displacement will be calculated from Xsens MVN Awinda position data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Displacement will be expressed in meters.

Baseline and immediately after the six-week intervention
Change in Vertical Center-of-Mass Displacement During Drop Vertical Jump Landing
Délai: Baseline and immediately after the six-week intervention

Vertical center-of-mass displacement will be calculated from Xsens MVN Awinda position data during landing load absorption, defined as the interval from peak vertical ground reaction force to maximum dominant-knee flexion. Displacement will be expressed in meters.

Baseline and immediately after the six-week intervention
Peak Knee Flexion Angle During the Reactive Drop Vertical Jump Task
Délai: Immediately after the six-week intervention

Peak dominant-knee flexion angle will be measured in degrees using the Xsens MVN Awinda system during a visually cued drop vertical jump. Participants will perform the task when a predetermined target color appears on the BlazePod system and withhold movement for other colors. Five successful trials will be recorded. Peak knee flexion will be identified during the landing deceleration phase, from initial ground contact to maximum dominant-knee flexion.

Immediately after the six-week intervention

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 novembre 2026

Achèvement primaire (Estimé)

1 novembre 2027

Achèvement de l'étude (Estimé)

1 novembre 2027

Dates d'inscription aux études

Première soumission

31 octobre 2026

Première soumission répondant aux critères de contrôle qualité

31 octobre 2026

Première publication (Réel)

5 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

5 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

31 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 61351342/020-2509

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

There are no plans to share individual participant data with other researchers. Study findings will be disseminated through aggregate results in scientific publications and presentations.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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