Sports Physical TherapyNCT07168681
The Effects of Visual Input on Cognitive Function, Physical Performance, and Postural Stability in Adolescent Male Basketball Players
A study of Sports Physical Therapy and Stroboscopic Visual Training, run by Hacettepe University.
Trial 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. Read more about this study
- Who is it for?
- Ages 14 to 19 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Sports Physical Therapy, Stroboscopic Visual Training, Cognitive Function
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 36 participants
- Where
- No sites listed yet
- Study dates
- 15 Sep 2025to 30 Oct 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 14 to 19 years
- Men only
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- Male basketball players aged 14-19 years
- With at least one year of basketball experience
- Minimum training frequency of two days per week.
Who cannot join
- 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)
About this study
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.
Read more
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.
- Conditions
- Sports Physical Therapy, Stroboscopic Visual Training, Cognitive Function, Physical Performance, Postural Stability
- Being tested
- Control group
- Keywords
- physical performance, stroboscopic visual training, cognitive function
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Control groupOther
Also called Exercise training under normal visual conditions
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.
| Study group | Role | What they receive |
|---|---|---|
| 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. Receives: 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. Receives: Other: Control group |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: Day 1, after the 6 weeks and after the 4 weeks
Secondary outcomes (5)
Static Postural stability
Postural stability will be assessed statically using the GYKO inertial sensor. The GYKO inertial sensor system (dimensions: 50 × 70 × 20 mm, weight: 35 g; Microgate, Bolzano, Italy) includes a three-dimensional accelerometer, gyroscope, and magnetometer, enabling data acquisition at a sampling frequency of 500 Hz (full-scale range: 8 g).
Measured: Day 1, after the 6 weeks and after the 4 weeks
Dynamic Postural stability
Dynamic postural stability will be assessed using the Lower Extremity Y Balance Test, which is employed to evaluate dynamic balance, mobility, and neuromuscular control.
Measured: Day 1, after the 6 weeks and after the 4 weeks
Change of direction ability
In the assessment of physical performance, change of direction ability, reactive agility, and jumping performance will be evaluated. The change-of-direction (COD) ability will be assessed using the V-Cut Test. The V-Cut Test is a valid and reliable COD assessment for young basketball players (ICC = 0.92) [26].
In this test, athletes perform a 25-meter sprint incorporating a 45° change of direction every 5 meters. The total completion time of the test is recorded.
Measured: Day 1, after the 6 weeks and after the 4 weeks
Reactive agility
In the assessment of physical performance, change of direction ability, reactive agility, and jumping performance will be evaluated. Reactive agility assess Y shaped test. The Y-Shaped Agility Test will be administered to evaluate reactive agility performance. This test is specifically designed to represent the change-of-direction movements and running patterns frequently encountered in basketball [29]. The protocol consists of a 5-meter straight sprint followed by a 45° change of direction to either the left or right side, followed by another 5-meter sprint. Athletes begin from a stationary position 30 cm behind the starting line, and timing is initiated once the first photocell gate is crossed. After completing the initial 5-meter sprint, the athlete changes direction to the predetermined side (left or right) and sprints an additional 5 meters. The timing is stopped when the athlete passes through the second photocell gate.
Measured: Day 1, after the 6 weeks and after the 4 weeks
Jumping Performance
In the assessment of physical performance, change of direction ability, reactive agility, and jumping performance will be evaluated. Jump performance will be assessed using the My Jump Lab application.
Athletes will perform one familiarization trial at submaximal effort, followed by a 1-minute rest period, and then complete three vertical jumps.
The validity and reliability of the My Jump Lab application have been previously demonstrated.
Measured: Day 1, after the 6 weeks and after the 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Sep 2025
- Study start15 Sep 2025 (estimated)
- Primary completion30 Sep 2027 (estimated)
- Study completion30 Oct 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Sports Physical TherapyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 36 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hacettepe University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Birgül Dıngırdan, Hacettepe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07168681
- Sponsor's protocol ID
- HÜ- FTR- BD- 5
- Status last verified
- Sep 2025
- First submitted
- 12 Aug 2025
- Last updated
- 11 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Dingirdan Gultekinler B, Uzlasir S, Tunay VB. Integrating stroboscopic visual perturbation into a neuromuscular warm-up in adolescent male basketball players: effects on cognitive function, physical performance, and postural stability-a randomized controlled trial. BMC Sports Sci Med Rehabil. 2026 May 14;18(1):303. doi: 10.1186/s13102-026-01748-z.
PubMed 42135790
Study at a glance
From the registry record, last updated by the sponsor on 11 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effects of Visual Input on Cognitive Function, Physical Performance, and Postural Stability in Adolescent Male Basketball Players
- ClinicalTrials.gov ID
- NCT07168681
- Acronym / sponsor ID
- HÜ- FTR- BD- 5
- Conditions
- Sports Physical Therapy, Stroboscopic Visual Training, Cognitive Function, Physical Performance, Postural Stability
- Keywords
- physical performance, stroboscopic visual training, cognitive function
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 36 participants (estimated)
- Lead sponsor
- Hacettepe UniversityUniversity, hospital or other
- Study start
- 15 Sep 2025 (estimated)
- Primary completion
- 30 Sep 2027 (estimated)
- Study completion
- 30 Oct 2027 (estimated)
- First posted
- 11 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Stroboscopic visual training group | Experimental | Other: Control groupThe 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. |
| Control group | Active comparator | Other: Control groupThe 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. |
Who may qualify
- Ages
- 14 to 19 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (3 listed)
- Male basketball players aged 14-19 years
- With at least one year of basketball experience
- Minimum training frequency of two days per week.
Key exclusion criteria (6 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Control groupAlso: Exercise training under normal visual conditionsActive 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. | Other | Control group, Stroboscopic visual training group |
Primary outcome
Cognitive function
Time frame: Day 1, after the 6 weeks and after the 4 weeks
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.
5 secondary outcomes
Static Postural stability
Time frame: Day 1, after the 6 weeks and after the 4 weeks
Dynamic Postural stability
Time frame: Day 1, after the 6 weeks and after the 4 weeks
Change of direction ability
Time frame: Day 1, after the 6 weeks and after the 4 weeks
Reactive agility
Time frame: Day 1, after the 6 weeks and after the 4 weeks
Jumping Performance
Time frame: Day 1, after the 6 weeks and after the 4 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Sep 2025.
- Derived from this study: PubMed 42135790Dingirdan Gultekinler B, Uzlasir S, Tunay VB. Integrating stroboscopic visual perturbation into a neuromuscular warm-up in adolescent male basketball players: effects on cognitive function, physical performance, and postural stability-a randomized controlled trial. BMC Sports Sci Med Rehabil. 2026 May 14;18(1):303. doi: 10.1186/s13102-026-01748-z.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
A study of Sports Physical Therapy and Stroboscopic Visual Training, run by Hacettepe University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 11 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cognitive function (time frame: Day 1, after the 6 weeks and after the 4 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07168681, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2025.