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Not yet recruiting NCT07503119

The Effect of Sport-Specific Visual and Vestibular Training in Open-Skill Athletes

No phase Interventional Open-Skill Athletes

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Pinhole Glass Training, T-Drill Agility Exercise, Letter Tracking Station, Sport-Specific Vestibulo-Ocular Reflex Training.
Who it may be relevant to
Registry conditions: Open-Skill Athletes. Basic parameters: 18 years — 23 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Sport-Specific Visual and Vestibular Training on Reaction Time and Dynamic Balance in Open-Skill Athletes

Overview

This study aims to examine the effects of a 6-week sport-specific visual and vestibular training program on athletes' reaction time and dynamic balance, while comparing outcomes with a control group to determine the extent to which the training contributes to performance improvements.

Detailed description

This pre-test and post-test experimental study will include 20 open-skill athletes randomly divided into two groups (n = 10 each): a control group and an intervention group.

The intervention group will participate in a 6-week sport-specific visual and vestibular training program conducted twice weekly, while the control group will continue their regular training and receive a one-time visual-vestibular educational brochure and online session. Reaction time and dynamic balance will be assessed at baseline and after the 6-week period. Reaction time will be measured using the Light Trainer system and dynamic/static balance will be evaluated using the ProKin 252 device.

Interventions

  • Other Pinhole Glass Training
    Participants work in 5-person groups using pinhole glasses to restrict peripheral vision, performing a continuous 5-minute ball-passing exercise using both upper and lower extremities.The exercise is repeated three times over a period of six weeks
  • Other T-Drill Agility Exercise
    Participants complete a T-shaped course with BlazePod® lights, reacting to randomly illuminated cones and returning to the center; the exercise is repeated three times. The exercise is repeated three times over a period of six weeks
  • Other Letter Tracking Station
    Participants perform Eye Letter Saccades tasks by reading sequences of letters and numbers with eye movements while performing rapid lower limb stepping; a ball is caught at the 20th second, repeated three times. The exercise is repeated three times over a period of six weeks.
  • Other Sport-Specific Vestibulo-Ocular Reflex Training
    Participants fixate on a target while moving their head up and down and stepping rapidly; a ball is caught at the 20th second, repeated three times. The exercise is repeated three times over a period of six weeks

Primary outcome measures

  • Simple Motor Reaction Time Test [Time frame: 6 weeks]
  • Hit the Dots Test [Time frame: 6 weeks]
  • Trail Making Test (Part B) [Time frame: 6 weeks]
  • ProKin 252, TecnoBody® Dynamic Balance Evaluation [Time frame: 6 weeks]
  • ProKin 252, TecnoBody® Static Balance Evaluation [Time frame: 6 weeks]

Eligibility criteria

Inclusion criteria

  • Athletes aged 18-23 years.
  • Possess an active sports license in any open-skill sport (e.g., volleyball, basketball, football, etc.).
  • No upper or lower extremity injury or surgery in the past three months.
  • Participate in regular training sessions throughout the study period.

Exclusion criteria

  • Having an injury in the last three months that required being away from training for more than two weeks.
  • Having undergone upper or lower extremity surgery in the last six months.
  • Having any neurological or cardiovascular condition.
  • Having any vestibular or visual disorder.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

Turkey (Türkiye) · 1 center
  • Yeditepe University — Ataşehir

Identifiers

NCT: NCT07503119 · Talyay

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗