NCT07584148

Brief Summary

This randomized controlled study aims to investigate the effects of neuroathletic training on dynamic visual acuity, endurance, balance, and injury risk in adolescent basketball players. Licensed basketball players aged 14-17 years will be randomly assigned to either a neuroathletic training group or a control group. The training group will receive sport-specific progressive neuroathletic exercises in addition to their regular basketball training for one week, while the control group will continue their usual training routine. Before and after the intervention, participants will be assessed for dynamic visual acuity, core muscle endurance, balance, functional movement, pain, and kinesiophobia. The findings of this study may help clarify whether neuroathletic training can improve performance-related outcomes and reduce injury risk in adolescent basketball players.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

February 15, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 26, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 12, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 29, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

May 13, 2026

Completed
Last Updated

May 13, 2026

Status Verified

May 1, 2026

Enrollment Period

8 months

First QC Date

April 29, 2026

Last Update Submit

May 6, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Functional Movement Screen (FMS) total score

    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.

    Baseline and immediately following the 1-week intervention

Secondary Outcomes (5)

  • Dynamic Visual Acuity (DVA)

    Baseline and immediately following the 1-week intervention

  • Balance Error Scoring System (BESS) / Denge Hata Puanlama Sistemi

    Baseline and immediately following the 1-week intervention

  • Core muscle endurance (Prone plank test)

    Baseline and immediately following the 1-week intervention

  • Tampa Scale for Kinesiophobia (TSK)

    Baseline and immediately following the 1-week intervention

  • Visual Analog Scale (VAS) for pain

    Baseline and immediately following the 1-week intervention

Study Arms (2)

Neuroathletic Training Group

EXPERIMENTAL
Other: neuroathletic training

Control group

NO INTERVENTION

Interventions

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.

Neuroathletic Training Group

Eligibility Criteria

Age14 Years - 17 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pamukkale University

Denizli, Pamukkale/Kınıklı, 20070, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Master's student

Study Record Dates

First Submitted

April 29, 2026

First Posted

May 13, 2026

Study Start

February 15, 2025

Primary Completion

October 26, 2025

Study Completion

January 12, 2026

Last Updated

May 13, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations