Neuroathletic Training Effects on Muscle Strength, Balance, and Cognition
Acute Effects of Neuroathletic Training on Posterior Chain Muscle Strength, Endurance, Proprioception, Dynamic Balance, and Cognitive Performance in Non-Athletic Individuals
1 other identifier
interventional
52
1 country
1
Brief Summary
Neuroathletic training is an innovative approach aimed at enhancing neurophysiological processes to improve motor control, reflex responses, balance, proprioception, and cognitive functions. While this method has shown promise in athletes, its acute effects on non-athletic individuals remain underexplored. The posterior chain (gluteus maximus, hamstrings, and erector spinae) plays a critical role in postural stability, movement, and injury prevention. Weakness in these muscles, coupled with poor balance and proprioception, may increase injury risk. Additionally, cognitive performance, including attention and reaction time, is vital for functional activities and may be enhanced through neuroathletic interventions. This study seeks to address the gap in understanding the acute effects of neuroathletic training on non-athletic individuals, providing evidence to support its integration into rehabilitation and injury prevention programs.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2025
Shorter than P25 for not_applicable
1 active site
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
April 11, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 13, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 15, 2025
CompletedFirst Submitted
Initial submission to the registry
August 5, 2025
CompletedFirst Posted
Study publicly available on registry
August 12, 2025
CompletedMarch 10, 2026
March 1, 2026
1 month
August 5, 2025
March 8, 2026
Conditions
Outcome Measures
Primary Outcomes (8)
Gluteus Maximus Muscle Strength (Newton)
Assessed using a digital handheld dynamometer (Lafayette Manual Muscle Tester, Model 01165) during maximal voluntary isometric contraction in prone hip extension. Three trials are conducted, and the highest value is recorded.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Erector Spinae Endurance (Seconds)
Evaluated using the Biering-Sørensen Test. Participants maintain a horizontal trunk position with the lower body fixed until fatigue. Time is recorded with a stopwatch.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Knee Joint Proprioception (Degrees)
Measured using an inclinometer to assess knee joint position sense. Angular deviation from 30° knee flexion target is recorded. The mean error across trials is used as the final score.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Dynamic Balance (Percent Reach Distance)
Assessed with the Y-Balance Test in three directions: anterior, posteromedial, and posterolateral. Reach distances are normalized to limb length and averaged to calculate dynamic balance performance.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Cognitive Performance - Stroop Test Reaction Time
Assesses selective attention and cognitive interference using the Stroop Color-Word Test. Reaction time is recorded in milliseconds during the incongruent trial phase.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Cognitive Performance - Stroop Test Error Count
Assesses accuracy during the Stroop Color-Word Test. The number of errors made during the incongruent trials is recorded.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Cognitive Performance - Trail Making Test Completion Time
Assesses visual attention and task-switching using Trail Making Test Parts A and B. Time to complete each part is recorded in seconds.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Cognitive Performance - Trail Making Test Error Count
Assesses accuracy during Trail Making Test Parts A and B. The number of errors committed during each test part is recorded.
Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post
Study Arms (2)
Neuroathletic Training
EXPERIMENTALParticipants will undergo a 20-minute neuroathletic training protocol using the Z-Health® kit, targeting visual, vestibular, and proprioceptive systems. The protocol includes visual reset exercises (eye massage, palming), star chart eye muscle training, saccade training with letter cards, convergence-divergence training, Brock string training, hip and spine extension exercises, saccule activation lunge exercises, slap tap coordination exercises, and pinhole glasses exercises to enhance motor control, balance, and cognitive performance.
Standard Warm-Up
ACTIVE COMPARATORParticipants will perform a 20-minute standard warm-up protocol consisting of 10 minutes of light walking at a moderate pace on flat terrain, followed by 10 minutes of dynamic stretching exercises (10 repetitions each of leg swings, hip flexor stretches, knee hugs, high knees, butt kicks, arm circles, and trunk rotations). This protocol serves as a control to compare against the neuroathletic training intervention.
Interventions
This 20-minute warm-up consists of two components: 10 minutes of light walking at a moderate pace and 10 minutes of dynamic stretching (leg swings, hip flexor stretches, knee hugs, high knees, butt kicks, arm circles, and trunk rotations). It is intended to mimic standard pre-activity routines and serves as the comparator condition.
This intervention involves a 20-minute neuroathletic training session using the Z-Health® kit. It includes visual reset exercises (eye massage, palming), star chart eye muscle training, saccade training with letter cards, convergence-divergence drills using Brock string, vestibular activation through lunges, spinal and hip extension exercises, slap tap coordination drills, and use of pinhole glasses. The aim is to stimulate sensory pathways and enhance neuromotor readiness acutely.
Eligibility Criteria
You may qualify if:
- Age 18-30 years.
- No regular physical activity in the past 6 months (IPAQ Short Form: physical activity level \>3000 MET-min/week excluded).
- Body Mass Index (BMI) 18.5-24.9 kg/m².
- No history of lower extremity injury or neurological conditions.
- Ability to perform study tests and exercises.
- Written informed consent.
You may not qualify if:
- Acute injury in the past 6 months.
- Chronic pain or postural deformities.
- Sensory impairments affecting study participation.
- Musculoskeletal, neurological, respiratory, or cardiovascular conditions limiting exercise.
- History of malignancy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Health Sciences, Gulhane Faculty of Physiotherapy and Rehabilitation
Ankara, Etlik, 06010, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The outcomes assessors, responsible for conducting and analyzing measurements (e.g., muscle strength, balance, proprioception, and cognitive tests), will be blinded to the group allocation of participants to minimize bias in data collection and interpretation. Participants, care providers, and investigators will not be blinded due to the nature of the intervention, which requires active participation and specific instructions for neuroathletic training or standard warm-up protocols.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
August 5, 2025
First Posted
August 12, 2025
Study Start
April 11, 2025
Primary Completion
May 13, 2025
Study Completion
July 15, 2025
Last Updated
March 10, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared due to institutional data protection policies and ethical considerations. The collected data are limited to the scope of the approved protocol and will only be used for internal analysis by the research team.