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Neuro-Athletic Training in Football

Optimizing Elite Football Performance Through Neuro-Athletic Training: A Parallel-Group Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07092735
Enrollment
56
Registered
2025-07-30
Start date
2024-06-12
Completion date
2024-08-12
Last updated
2025-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Athletic Performance, Neurocognitive Function, Proprioception, Soccer, Sensorimotor Integration, Eye Movements, Neuroathletic Training

Brief summary

This randomized controlled trial evaluates the effectiveness of an 8-week neuro-athletic training (NAT) program in enhancing sport-specific skills and physical capacities in elite male football players aged 18-23 years. Participants were randomly assigned to a NAT intervention group or a control group that maintained standard training. The NAT program involved oculomotor, vestibular, and proprioceptive drills. Primary outcomes include passing and shooting accuracy; secondary outcomes include flexibility and isokinetic knee strength.

Interventions

BEHAVIORALNeuro-Athletic Training

Participants receive a structured 8-week NAT program including oculomotor, vestibular, and proprioceptive drills, 3 sessions/week (35-45 minutes each).

Participants continue their standard in-season football training program without any NAT components.

Sponsors

Ankara Yildirim Beyazıt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Outcome assessments were performed by an independent physiotherapist who was blinded to group allocation to reduce measurement bias. Additionally, the researcher conducting the statistical analysis was also blinded to group assignments to ensure data objectivity. Participants and intervention providers were not blinded due to the nature of the behavioral intervention.

Intervention model description

This study used a parallel-group randomized controlled trial design with pre- and post-intervention assessments. Participants were randomly assigned to either a Neuro-Athletic Training (NAT) group or a control group. The NAT group received an 8-week structured program targeting sensorimotor integration through oculomotor, vestibular, and proprioceptive drills, while the control group continued standard football training without additional interventions. Outcome assessors and statistical analysts were blinded to group allocations. The study was conducted under standardized conditions to ensure methodological rigor and group comparability.

Eligibility

Sex/Gender
MALE
Age
18 Years to 23 Years
Healthy volunteers
Yes

Inclusion criteria

* Male football players aged 18-23 years * Active in the Turkish Regional Amateur League (2023-2024 season) * Minimum of 5 years of uninterrupted football training experience * No known neuromuscular or visual impairments * Participation in at least four football training sessions per week * Willingness and ability to participate in all assessments and training sessions * Provision of written informed consent

Exclusion criteria

* History of orthopedic or neurological surgery within the past year * Acute or chronic musculoskeletal injuries preventing full participation * Uncorrected visual impairment * Use of medications affecting neuromuscular performance or coordination * Previous or concurrent involvement in structured neuromuscular or neuro-athletic training programs * Irregular attendance to training sessions (\>20% missed) * Any condition precluding safe participation, as determined by medical staff

Design outcomes

Primary

MeasureTime frameDescription
Passing Accuracy (Mor-Christian Passing Test)Pre-intervention (baseline) and post-intervention (after 8 weeks).Measured as a score (max 120) based on 12 passes from 7, 8.5, and 10 meters toward a mini-goal. Assessed pre- and post-intervention.
Shooting Accuracy (Mor-Christian Shooting Test)Pre-intervention (baseline) and post-intervention (after 8 weeks).Measured as a score (max 80) based on 16 shots from 14.5 meters toward four 45 cm targets. Assessed pre- and post-intervention.

Secondary

MeasureTime frameDescription
Flexibility (Sit-and-Reach Test)Pre-intervention (baseline) and post-intervention (after 8 weeks)Measured in centimeters using a standard sit-and-reach box, assessing hamstring and lower back flexibility.
Isokinetic Knee Strength (ISOMED 2000 Dynamometer)Pre-intervention (baseline) and post-intervention (after 8 weeks).Concentric peak torque of quadriceps and hamstrings at 60°/s (5 repetitions) and 180°/s (15 repetitions), normalized to body mass (Nm/kg), and hamstring-to-quadriceps (H:Q) ratio.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026