- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07409155
Effects of a SVT on Agility and Reactive Agility in Adolescent Male Basketball Players
Effects of a Six-Week Stroboscopic Training Program on Agility and Reactive Agility in Adolescent Male Basketball Players: A Pilot Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim of this pilot study was to investigate the effects of a stroboscopic training intervention on reactive agility and agility speed in basketball players, using identical movement patterns, and to evaluate perceptual-cognitive indices derived from the relationship between agility and reactive agility performance. This study hypothesized that stroboscopic visual training would significantly improve reactive agility and agility performance in adolescent male basketball players. This study was designed as a single-blind randomized controlled trial, with the statistician blinded during the data analysis. This study was conducted at Kocaeli İzmitspor and Bulls Basketball Sports Clubs. As the study population consisted of adolescent athletes, written informed consent was obtained from their parents or legal guardians. Prior to data collection, all participants were informed about the purpose and procedures of the study, the voluntary nature of participation, and their right to withdraw at any time without any consequences. Confidentiality and anonymity of the participants were assured, and it was stated that all data would be used exclusively for scientific purposes. Inclusion criteria: Male basketball players aged 14-18 years who had at least one year of basketball experience and trained a minimum of two days per week.
Exclusion criteria: Athletes who did not consent to participate in the study; those with a history of upper or lower extremity surgery within the past year; those who had sustained any musculoskeletal injury to the upper or lower extremities within the last month; and individuals with a history of neurological disorders, epilepsy, or a diagnosis of attention-deficit/hyperactivity disorder (ADHD).
Participants were randomly allocated to either the stroboscopic visual exercise group (SVT, n = 5) or the control group (CON, n = 5) using a computer-generated randomization list. The SVT group performed basketball-specific neuromuscular warm-up exercises combined with stroboscopic glasses (Senaptec Strobe, Beaverton, ABD) at a duty cycle of 100 ms clear/150 ms opaque twice per week, whereas the CON group completed the identical neuromuscular warm-up exercise protocol under normal visual conditions without visual perturbation.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Yeni Mahalle
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Sakarya, Yeni Mahalle, Turkey (Türkiye), 54400
- Birgul Dingirdan Gultekinler
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male basketball players aged 14-18 years who had at least one year of basketball experience and trained a minimum of two days per week.
Exclusion Criteria:
- Athletes who did not consent to participate in the study; those with a history of upper or lower extremity surgery within the past year; those who had sustained any musculoskeletal injury to the upper or lower extremities within the last month; and individuals with a history of neurological disorders, epilepsy, or a diagnosis of attention-deficit/hyperactivity disorder (ADHD).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Stroboscopic visual training group (SVT)
The SVT group performed basketball-specific neuromuscular warm-up exercises combined with stroboscopic glasses (Senaptec Strobe, Beaverton, ABD) at a duty cycle of 100 ms clear/150 ms opaque twice per week.
Specifically, stroboscopic eyewear alternates between transparent and opaque phases at adjustable frequencies, thereby restricting the amount and continuity of visual information available to the athlete.
This controlled visual disruption is thought to activate neural networks involved in visual and cognitive processing, compelling athletes to perceive, decide, and respond under conditions of reduced or intermittent visual input.
|
The SVT group performed basketball-specific neuromuscular warm-up exercises combined with stroboscopic glasses (Senaptec Strobe, Beaverton, ABD) at a duty cycle of 100 ms clear/150 ms opaque twice per week, whereas the control group completed the identical neuromuscular warm-up exercise protocol under normal visual conditions without visual perturbation.
Specifically, stroboscopic eyewear alternates between transparent and opaque phases at adjustable frequencies, thereby restricting the amount and continuity of visual information available to the athlete.
This controlled visual disruption is thought to activate neural networks involved in visual and cognitive processing, compelling athletes to perceive, decide, and respond under conditions of reduced or intermittent visual input.
|
|
Other: Control group
Control group completed the identical neuromuscular warm-up exercise protocol under normal visual conditions without visual perturbation.
|
The control group completed the identical neuromuscular warm-up exercise protocol under normal visual conditions without visual perturbation.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reactive agility
Time Frame: Before the exercise program, after the exercise program and 4 weeks after
|
Reactive agility performance was assessed using the Y-shaped agility test.
The Y-shaped agility test was administered using a Witty photocell gate.
The 45° angle between the midpoint of the trigger gate and the midpoints of the target gates was determined using a goniometer, and the photoelectric cells were positioned on the inner sides of the gates.
Participants began the test 30 cm behind the start line and sprinted maximally through the first two gates.
Immediately after completing the 5-m linear sprint by passing through the first two gates, a visual stimulus appeared on the computer screen positioned in front of the athletes.
When the letter "A" was displayed, the athletes were instructed to sprint toward the cone labeled A, whereas when the letter "B" appeared, they were required to sprint toward the cone labeled B as quickly as possible.
The fastest time obtained from the three trials was used for the statistical analysis.
|
Before the exercise program, after the exercise program and 4 weeks after
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Agility
Time Frame: Before the exercise program, after the exercise program and 4 weeks after
|
Agility performance was also assessed using the Y-shaped agility test.
Prior to each trial, the athletes were informed of the direction of the turn.
They were instructed to perform the change-of-direction task, which involved an approximately 45° directional change, as quickly as possible.
In addition, athletes were instructed not to initiate the change of direction before passing through the trigger gate.
Three trials were completed for each direction (left and right), and the fastest trial for each direction was included in the analysis.
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Before the exercise program, after the exercise program and 4 weeks after
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
REAC-INDEX
Time Frame: Before the exercise program, after the exercise program and 4 weeks after
|
The REAC-INDEX, calculated as the difference between reactive agility and agility speed, was used as an indirect indicator (proxy) of perceptual-cognitive load during reactive agility performance. REAC- INDEX (ms)= RA (ms)- A (ms) |
Before the exercise program, after the exercise program and 4 weeks after
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SUBU 4
- 29.12.2025/ 2025.12.20 (Other Identifier: Ethics Committee for Non-Interventional Clinical Research Publications, Nevşehir Hacı Bektaş Veli University)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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