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Investigation of the Effects of Exercises Performed With Stroboscopic Glasses on Athletic Performance in Volleyball Players

NCT07323108 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-01-07

No results posted yet for this study

Summary

The aim of this study was to examine the effects of exercises performed with stroboscopic glasses on athletic performance in volleyball players. 40 professional male volleyball players aged between 18-35, who had not undergone any surgery in the last 6 months and who had no chronic systemic disease were included in the study. 20 individuals were randomly assigned to the stroboscopic glasses group and 20 individuals to the control group. Individuals in the stroboscopic glasses group were informed about stroboscopic glasses. Individuals in the stroboscopic glasses group wore glasses and individuals in the control group did their exercises without glasses for 6 weeks. Individuals' visual reaction time, auditory reaction time and target-oriented reaction time were measured with the Human Benchmark test, agility assessment with the T Agility test, anaerobic capacity assessment with the vertical jump test, balance assessment with the Flamingo Balance test and coordination assessment with the Hexagonal Coordination test. The evaluations were made three times, before exercise, 6 weeks after exercise and 10 weeks after exercise.

Conditions

  • Stroboscopic Glasses

Interventions

DEVICE

stroboscopic visual training

40 volleyball players were evaluated at three times: pre-exercise, after 6 weeks and after 10 weeks regard to reaction time, agility, anaerobic performance, balance and coordination. Experimental group used stroboscopic glasses when doing exercise. Exercise program consisted lunge, jumping and balance exercises. Each exercise consisted 12 repetitions and 3 sets. Stroboscopic glasses were adjusted to 100 ms on/150 ms off flash level 3. This frequency is always preferred scientific research about stroboscopic visual training.

Sponsors & Collaborators

  • Baskent University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-01
Primary Completion
2025-02-01
Completion
2025-02-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07323108 on ClinicalTrials.gov