Effects Of Stroboskobic Visual Training On Cognitive Performance in Adolescent Male Volleyball Pl… (NCT07162545) | Clinical Trial Compass
CompletedNot Applicable
Effects Of Stroboskobic Visual Training On Cognitive Performance in Adolescent Male Volleyball Players.
Turkey (Türkiye)34 participantsStarted 2025-10-30
Plain-language summary
Objective: To determine the effects of a stroboscopic training program on cognitive function in adolescent male volleyball players. The study aims to reveal the impact of using stroboscopic glasses during a portion of their training on volleyball players' cognitive functions.
The data obtained from the study will be important for improving volleyball training programs and contributing to the sports science literature.
Who can participate
Age range
13 Years – 18 Years
Sex
MALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Being an adolescent male volleyball player between the ages of 13-18.
* Having attended volleyball training regularly for at least one year.
* Agreeing to attend training regularly throughout the study period.
* Having signed the voluntary participation form and parental consent form.
* Having no visual or auditory impairments.
* Having completed cognitive function tests during the initial evaluation.
Exclusion Criteria:
* Having a history of a disease that could affect neurological, psychiatric, or cognitive functions.
* Individuals whose use of glasses, contact lenses, or eye health prevents them from using stroboscopic glasses.
* Having had a head, neck, or serious lower/upper extremity injury within the last 6 months.
* Regular use of any medication (especially medications that affect attention/cognitive functions).
* Individuals who declared they were unable to comply with the study process or who did not participate in follow-up assessments.
* Individuals who did not comply with the research protocol during testing or whose data were incomplete.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.