NCT07168681

Brief Summary

The aim of this study is to investigate the effects of exercises performed with stroboscopic glasses-recently gaining popularity in sports-on cognitive function, physical performance, and postural stability, which are among the key skills in athletic performance. The originality of the study lies in being the first to examine the effects of stroboscopic glasses-based exercises on basketball players. Hypotheses of the study: H1: Exercises performed with stroboscopic glasses have an effect on athletes' cognitive functions. H2: Exercises performed with stroboscopic glasses have an effect on athletes' physical performance. H3: Exercises performed with stroboscopic glasses have an effect on athletes' static and dynamic postural stability.

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
18mo left

Started Sep 2025

Typical duration for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress30%
Sep 2025Oct 2027

First Submitted

Initial submission to the registry

August 12, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

September 11, 2025

Completed
4 days until next milestone

Study Start

First participant enrolled

September 15, 2025

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2027

Last Updated

September 11, 2025

Status Verified

September 1, 2025

Enrollment Period

2 years

First QC Date

August 12, 2025

Last Update Submit

September 4, 2025

Conditions

Keywords

physical performancestroboscopic visual trainingcognitive function

Outcome Measures

Primary Outcomes (1)

  • Cognitive function

    It is planned to conduct the assessment using the Central Nervous System Vital Signs test battery. The Central Nervous System Vital Signs is a computer-based neurocognitive test battery with established validity and reliability, and is utilized in 66 countries.

    Day 1, after the 6 weeks and after the 4 weeks

Secondary Outcomes (5)

  • Static Postural stability

    Day 1, after the 6 weeks and after the 4 weeks

  • Dynamic Postural stability

    Day 1, after the 6 weeks and after the 4 weeks

  • Change of direction ability

    Day 1, after the 6 weeks and after the 4 weeks

  • Reactive agility

    Day 1, after the 6 weeks and after the 4 weeks

  • Jumping Performance

    Day 1, after the 6 weeks and after the 4 weeks

Study Arms (2)

Stroboscopic visual training group

EXPERIMENTAL

The exercise program to be implemented within the scope of the study is the SHRed (Sports Injury Prevention for the Lower Extremity, focusing on musculoskeletal and head-related injuries) neuromuscular training program. The program will be administered over six weeks, with two sessions per week. In the experimental group, the exercises will be performed using stroboscopic glasses. For the experimental group, the exercises with stroboscopic glasses will be administered in intervals of 2.5 minutes of exercise followed by 2.5 minutes of rest.

Other: Control group

Control group

ACTIVE COMPARATOR

The exercise program to be implemented within the scope of the study is the SHRed (Sports Injury Prevention for the Lower Extremity, focusing on musculoskeletal and head-related injuries) neuromuscular training program. The program will be administered over six weeks, with two sessions per week. Participants will be randomly assigned into two groups. The experimental group will perform the exercises while wearing stroboscopic glasses, whereas the control group will perform the exercises under normal visual conditions.

Other: Control group

Interventions

Active Comparator: Control group The exercise program to be implemented within the scope of the study is the SHRed (Sports Injury Prevention for the Lower Extremity, focusing on musculoskeletal and head-related injuries) neuromuscular training program. The program will be administered over six weeks, with two sessions per week. The control group will perform the exercises under normal visual conditions. The exercise program to be implemented within the scope of the study is the SHRed (Sports Injury Prevention for the Lower Extremity, focusing on musculoskeletal and head-related injuries) neuromuscular training program. The program will be administered over six weeks, with two sessions per week. Previous research has shown that the SHRed injury prevention neuromuscular training program reduces ankle and knee injuries in youth basketball players by 36% \[35\]. The program consists of balance, agility, strength, and aerobic exercises.

Also known as: Exercise training under normal visual conditions
Control groupStroboscopic visual training group

Eligibility Criteria

Age14 Years - 19 Years
Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Male basketball players aged 14-19 years
  • With at least one year of basketball experience
  • Minimum training frequency of two days per week.

You may not qualify if:

  • Not willing to participate in the study
  • A history of any upper or lower extremity surgery within the past year
  • A history of any musculoskeletal injury in the upper or lower extremities within the past month
  • The presence of a neurological disorder
  • A history of epilepsy
  • A diagnosis of attention deficit hyperactivity disorder (ADHD)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Control Groups

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Student

Study Record Dates

First Submitted

August 12, 2025

First Posted

September 11, 2025

Study Start

September 15, 2025

Primary Completion (Estimated)

September 30, 2027

Study Completion (Estimated)

October 30, 2027

Last Updated

September 11, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share