- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07392385
Neuro-Psychophysiological Characteristics of Athletes With Varying Levels of Experience (NEPSY-SPORT)
Effects of Volleyball-Specific Stroboscopic Training on Neuro-Psychophysiological Responses Across Different Experience Levels: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study is designed as a randomized controlled trial to examine the effects of volleyball-specific stroboscopic training on neuro-psychophysiological outcomes in athletes with different levels of competitive experience. Female volleyball players aged 10-16 years will be classified into three experience-based groups (novice, intermediate, and elite) according to their training history. Within each experience level, participants will be randomly assigned to either a stroboscopic training group or a control group, resulting in six study groups in total.
All participants will continue their routine volleyball training throughout the study period. In addition, athletes in the intervention group will complete an 8-week volleyball-specific stroboscopic training program, performed three times per week for a total of 24 sessions. Each training session will last approximately 35 minutes and will consist of volleyball-related drills, including passing, setting, receiving, rotation-based movements, and reaction-based tasks. Participants in the stroboscopic training group will perform these drills while wearing stroboscopic glasses with progressively adjusted visual disruption parameters, whereas the control group will perform the same drills under normal visual conditions.
Neuro-psychophysiological assessments will be conducted before and after the training period. Primary and secondary outcome measures will include heart rate variability, electrodermal activity, functional near-infrared spectroscopy recordings of prefrontal cortical activity, dual-task performance under varying levels of cognitive-motor demand, and eye-tracking parameters such as pupil diameter and fixation behavior. Psychological measures will also be collected using validated self-report instruments.
All measurements will be performed under standardized laboratory conditions. The study aims to determine whether stroboscopic training leads to differential neuro-psychophysiological adaptations across experience levels and whether such adaptations are associated with improved regulation of cognitive, physiological, and perceptual-motor processes relevant to volleyball performance.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Merkez
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Yozgat, Merkez, Turkey (Türkiye), 66100
- Yozgat Bozok University Faculty of Sport Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Female volleyball players aged 10 to 16 years
- Actively competing in organized volleyball
- Regular participation in team training sessions
- Classified as novice, intermediate, or elite based on training experience
- Written parental/legal guardian informed consent and participant assent obtained
Exclusion Criteria:
- Presence of any chronic medical condition affecting study outcomes
- Use of supplements or medications that may influence performance
- Current injury or participation in a rehabilitation program
- Failure to attend scheduled training sessions
- Inability to complete baseline or post-intervention assessments
- Injury occurring during the study period that prevents continued participation
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Stroboscopic Training Group
Participants will continue their regular volleyball training and perform the same volleyball-specific drills as the intervention group for 8 weeks.
All exercises will be completed under normal visual conditions without the use of stroboscopic glasses.
|
Participants will perform volleyball-specific training drills while wearing stroboscopic glasses that intermittently restrict visual input.
The training will be conducted three times per week for 8 weeks, totaling 24 sessions.
Each session will last approximately 35 minutes and will include volleyball-specific drills such as passing, setting, receiving, rotation-based movements, and reaction-based tasks.
Visual disruption parameters of the stroboscopic glasses will be progressively adjusted throughout the intervention period.
|
|
Active Comparator: Control Group
Participants will continue their regular volleyball training and perform the same volleyball-specific drills as the intervention group for 8 weeks.
All exercises will be completed under normal visual conditions without the use of stroboscopic glasses.
|
Participants will perform the same volleyball-specific training drills as the intervention group for 8 weeks under normal visual conditions, without the use of stroboscopic glasses.
Training frequency, duration, and drill content will be matched to the intervention group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prefrontal Cortical Activation (fNIRS)
Time Frame: Baseline (pre-intervention) and immediately after the 8-week intervention.
|
Change in oxygenated and deoxygenated hemoglobin concentrations in the prefrontal cortex measured by functional near-infrared spectroscopy during dual-task performance
|
Baseline (pre-intervention) and immediately after the 8-week intervention.
|
|
Heart Rate Variability (HRV)
Time Frame: Baseline (pre-intervention) and immediately after the 8-week intervention.
|
Change in heart rate variability indices reflecting autonomic nervous system regulation, assessed at rest using a photoplethysmography-based system.
|
Baseline (pre-intervention) and immediately after the 8-week intervention.
|
|
Dual-Task Performance
Time Frame: Baseline (pre-intervention) and immediately after the 8-week intervention.
|
Change in reaction time and task performance under increasing levels of cognitive-motor demand assessed using a standardized dual-task protocol.
|
Baseline (pre-intervention) and immediately after the 8-week intervention.
|
|
Electrodermal Activity (EDA)
Time Frame: Baseline (pre-intervention) and immediately after the 8-week intervention.
|
Change in skin conductance responses reflecting sympathetic nervous system activity recorded during task performance.
|
Baseline (pre-intervention) and immediately after the 8-week intervention.
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|
Eye-Tracking Measures
Time Frame: Baseline (pre-intervention) and immediately after the 8-week intervention.
|
Change in pupil diameter, fixation duration, and visual search behavior assessed using a wearable eye-tracking system during dual-task performance.
|
Baseline (pre-intervention) and immediately after the 8-week intervention.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological Status (Depression, Anxiety, Stress)
Time Frame: Baseline (pre-intervention) and immediately after the 8-week intervention.
|
Change in self-reported depression, anxiety, and stress levels assessed using a validated questionnaire.
|
Baseline (pre-intervention) and immediately after the 8-week intervention.
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Zhong X, Dai Y, Xu M, Jiang C. Volleyball training improves working memory in children aged 7 to 12 years old: an fNIRS study. Cereb Cortex. 2024 Jul 3;34(7):bhae275. doi: 10.1093/cercor/bhae275.
- Zwierko M, Jedziniak W, Popowczak M, Rokita A. Effects of six-week stroboscopic training program on visuomotor reaction speed in goal-directed movements in young volleyball players: a study focusing on agility performance. BMC Sports Sci Med Rehabil. 2024 Feb 29;16(1):59. doi: 10.1186/s13102-024-00848-y.
- Guo J, Zhao L, Liu G, Li H, Wu J. Stroboscopic training effects on athletic performance and cognitive function across populations, purposes, and skill types: a systematic review and meta-analysis of randomized controlled trials. Front Sports Act Living. 2025 Dec 11;7:1705693. doi: 10.3389/fspor.2025.1705693. eCollection 2025.
- Piva T, Zerbini V, Barducco A, Mancioppi S, Raisi A, Vassali M, Bianchini G, Laporta M, Menegatti E, Grazzi G, Mazzoni G, Mandini S. Reduction in reaction time and improved oculomotor function following football-specific vision training in young players. BMC Sports Sci Med Rehabil. 2025 Oct 16;17(1):298. doi: 10.1186/s13102-025-01368-z.
- Bherer L, Kramer AF, Peterson MS, Colcombe S, Erickson K, Becic E. Transfer effects in task-set cost and dual-task cost after dual-task training in older and younger adults: further evidence for cognitive plasticity in attentional control in late adulthood. Exp Aging Res. 2008 Jul-Sep;34(3):188-219. doi: 10.1080/03610730802070068.
- Beavan A, Hanke L, Spielmann J, Skorski S, Mayer J, Meyer T, Fransen J. The effect of stroboscopic vision on performance in a football specific assessment. Sci Med Footb. 2021 Nov;5(4):317-322. doi: 10.1080/24733938.2020.1862420. Epub 2020 Dec 20.
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
Keywords
Other Study ID Numbers
- Bozok-SBF-IK-2025
- 124C195 (Other Identifier: The Scientific Research Project Fund of Yozgat Bozok University (TÜBİTAK))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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