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Neuroathletic TrainingNCT07584148

Neuroathletic Training in Adolescent Basketball Players

A study testing neuroathletic training in people with Neuroathletic Training and Adolescent Basketball Players, run by Pamukkale University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 14 to 17 yearsHealthy volunteers can take part
What is being tested?
neuroathletic training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Feb 2025to 12 Jan 2026
Phase
Interventional
Are there results?
None posted in the registry

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 17 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Pamukkale University

    Denizli, Pamukkale/Kınıklı, 20070

Other trials in Turkey (Türkiye)

About this study

Official title: Effects of Neuroathletic Training on Dynamic Visual Acuity, Endurance, Balance, Kinesiophobia, and Injury Risk in Adolescent Basketball Players: A Randomized Controlled Trial

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.

Being tested
neuroathletic training

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • neuroathletic trainingOther

    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.

Study groups in NCT07584148
Study groupRoleWhat they receive
Neuroathletic Training GroupExperimentalNot described
Receives: Other: neuroathletic training
Control groupNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: Baseline and immediately following the 1-week intervention

Secondary outcomes (5)
  1. Dynamic Visual Acuity (DVA)

    Dynamic visual acuity assessed using a visual chart while the participant performs active horizontal head movements. The lowest clearly read line will be recorded.

    Measured: Baseline and immediately following the 1-week intervention

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

    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.

    Measured: Baseline and immediately following the 1-week intervention

  3. Core muscle endurance (Prone plank test)

    Core endurance assessed by the duration the participant maintains the correct prone plank position. Longer duration indicates better core endurance.

    Measured: Baseline and immediately following the 1-week intervention

  4. Tampa Scale for Kinesiophobia (TSK)

    Kinesiophobia assessed using the Tampa Scale for Kinesiophobia. Higher scores indicate greater fear of movement.

    Measured: Baseline and immediately following the 1-week intervention

  5. Visual Analog Scale (VAS) for pain

    Pain intensity assessed using a 100-mm visual analog scale, with higher scores indicating greater pain intensity.

    Measured: Baseline and immediately following the 1-week intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 May 2026
  2. Study start15 Feb 2025
  3. Primary completion26 Oct 2025
  4. Study completion12 Jan 2026

Resources

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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07584148
Sponsor's protocol ID
PAU-FTR-GG-01
Status last verified
May 2026
First submitted
29 Apr 2026
Last updated
13 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing neuroathletic training in people with Neuroathletic Training and Adolescent Basketball Players, run by Pamukkale University at 1 site in Turkey (Türkiye).

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 1 inclusion and 1 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: finished, as of the sponsor's last update on 13 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Functional Movement Screen (FMS) total score (time frame: Baseline and immediately following the 1-week intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 13 May 2026.

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