- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07584148
Neuroathletic Training in Adolescent Basketball Players
Effects of Neuroathletic Training on Dynamic Visual Acuity, Endurance, Balance, Kinesiophobia, and Injury Risk in Adolescent Basketball Players: A Randomized Controlled Trial
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Pamukkale/Kınıklı
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Denizli, Pamukkale/Kınıklı, Turkey (Türkiye), 20070
- Pamukkale University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Aged between 14 and 17 years, Being a professional or amateur basketball player, Participating in sports for at least five hours per week and having engaged in the sport for a minimum of two years, Having no cognitive or motor dysfunction, Providing written informed consent signed by the parents/legal guardians.
Exclusion Criteria:
Reporting a back or lower extremity injury within the previous six months, Having any relevant medical history or current condition that could affect the balance system or perception-action system (e.g., neurological disorders, inner ear disorders, or color blindness), Using medications or substances that could affect balance and visual-motor reaction time performance.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control group
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Experimental: Neuroathletic Training Group
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This intervention is a progressive neuroathletic training program developed by the research team to improve motor skills, balance, eye coordination, and vestibular function in adolescent basketball players.
The program is performed for approximately 20 minutes per day over 6 days and includes visual relaxation exercises, eye massage, unilateral vertical jumping, Brock string training, shoulder/wrist/ankle circular movements, sacculus activation, cerebellar activation, and antisaccade exercises.
The content is progressively advanced across days by integrating balance challenges and visual-vestibular tasks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Movement Screen (FMS) total score
Time Frame: Baseline and immediately following the 1-week intervention
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Assessment of injury risk and movement quality using the Functional Movement Screen total score.
The test consists of 7 movement patterns scored from 0 to 3, with higher scores indicating better functional movement quality and lower injury risk.
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Baseline and immediately following the 1-week intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dynamic Visual Acuity (DVA)
Time Frame: Baseline and immediately following the 1-week intervention
|
Dynamic visual acuity assessed using a visual chart while the participant performs active horizontal head movements.
The lowest clearly read line will be recorded.
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Baseline and immediately following the 1-week intervention
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Balance Error Scoring System (BESS) / Denge Hata Puanlama Sistemi
Time Frame: Baseline and immediately following the 1-week intervention
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Postural stability assessed by the number of balance errors performed in double-leg, single-leg, and tandem stance conditions.
Lower scores indicate better balance performance.
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Baseline and immediately following the 1-week intervention
|
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Core muscle endurance (Prone plank test)
Time Frame: Baseline and immediately following the 1-week intervention
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Core endurance assessed by the duration the participant maintains the correct prone plank position.
Longer duration indicates better core endurance.
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Baseline and immediately following the 1-week intervention
|
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Tampa Scale for Kinesiophobia (TSK)
Time Frame: Baseline and immediately following the 1-week intervention
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Kinesiophobia assessed using the Tampa Scale for Kinesiophobia.
Higher scores indicate greater fear of movement.
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Baseline and immediately following the 1-week intervention
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Visual Analog Scale (VAS) for pain
Time Frame: Baseline and immediately following the 1-week intervention
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Pain intensity assessed using a 100-mm visual analog scale, with higher scores indicating greater pain intensity.
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Baseline and immediately following the 1-week intervention
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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
Other Study ID Numbers
- PAU-FTR-GG-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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