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Effects of Mental Fatigue Duration on Cortical Activity and Jump Performance (MF-CMJ-EEG)

2026年8月4日 更新者:Oğuzhan Bozkurt、Inonu University

Duration-Dependent Effects of Mental Fatigue on Cortical Activation Patterns and Lower-Limb Explosive Performance

"This study investigates whether the length of time spent on a mentally demanding task affects brain activity and jumping performance in physically active young men. Twelve healthy male university students, all regularly engaged in sport, completed four separate testing sessions on different days, each at least 72 hours apart. In one session (the control condition), participants watched a calm nature documentary. In the other three sessions, mental fatigue was induced by having participants perform a demanding attention task (the Stroop color-word test) continuously for 10, 15, or 30 minutes. Before and after each session, brain activity was recorded using electroencephalography (EEG), a painless method that measures electrical activity through sensors placed on the scalp. Immediately afterward, participants performed a countermovement jump test, a standard measure of explosive leg power used in sports science. The study examines whether longer periods of mental fatigue produce progressively larger changes in brain activity and jump performance, and whether changes in brain activity are related to changes in jumping ability. The findings may help athletes, coaches, and students better understand how mentally tiring activities, such as studying or exams, could affect physical performance shortly afterward."

研究概览

详细说明

"Mental fatigue is a psychobiological state induced by prolonged demanding cognitive activity, characterized by subjective tiredness and measurable decrements in sustained attention and executive control. While mental fatigue has been linked to impairments in endurance, strength, and anaerobic performance, evidence regarding explosive, single-effort tasks such as the countermovement jump (CMJ) remains sparse and inconsistent, and it remains unclear whether the cortical and behavioral consequences of mental fatigue scale with the duration of the inducing cognitive task.

This study used a single-group, repeated-measures crossover design in which the same twelve participants completed a non-fatiguing control condition and three graded mental-fatigue protocols (10, 15, and 30 minutes of continuous Stroop-task performance), with session order counterbalanced across participants and a minimum 72-hour washout between sessions. All sessions were conducted in the same laboratory within a consistent daily time window (10:00 ± 1 hour) to minimize circadian confounds.

Resting-state EEG (spectral power in delta, theta, alpha, and beta bands; theta/alpha and theta/beta ratios; spectral and sample entropy; frontal theta and posterior alpha) and subjective fatigue (0-10 visual analogue scale) were assessed immediately before and after each condition. Countermovement-jump height and its kinetic/kinematic correlates were then measured to evaluate explosive lower-limb power, the study's primary outcome; EEG parameters were treated as secondary, mechanistic outcomes.

Data were analyzed using repeated-measures ANOVA, Holm-Bonferroni-corrected Friedman/Wilcoxon tests where appropriate, and repeated-measures correlation to examine the relationship between post-intervention EEG parameters and CMJ performance. The study tested the hypothesis that increasing Stroop-task duration would produce progressively larger shifts in EEG-derived cortical activation and parallel reductions in CMJ performance, and that these neurophysiological and performance changes would be significantly associated with one another."

研究类型

介入性

注册 (实际的)

12

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

是的

描述

Inclusion Criteria:

  • Healthy male volunteers aged 18-30 years
  • Enrolled in the Faculty of Sport Sciences at İnönü University
  • Engaged in structured exercise at least three days per week
  • Free of any neurological, psychiatric, cardiovascular, or musculoskeletal disorder
  • Normal or corrected-to-normal vision
  • Physically capable of completing the experimental protocol safely

Exclusion Criteria:

  • Diagnosed neurological, psychiatric, cardiovascular, or musculoskeletal disorder
  • Lower-limb injury within the preceding 6 months
  • Use of medication known to affect central nervous system function
  • Prior diagnosis of a sleep disorder
  • Uncorrectable visual impairment or any disturbance of color perception
  • Cognitive or sensory limitation likely to interfere with performance of the Stroop task
  • Failure to complete a session in full, non-compliance with investigator instructions during testing, inability to produce an EEG recording of analyzable quality for technical reasons, or discontinuation of the experimental procedure for any reason
  • Non-compliance with pre-session restrictions (vigorous physical exercise or alcohol consumption within 24 hours before each session; caffeine, energy drinks, or other stimulant substances within 12 hours before each session)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
假比较器:Control
Participants viewed a neutral, cognitively undemanding nature documentary for a duration matched to the mental-fatigue protocols, without performing the Stroop task.
Viewing of a neutral, cognitively undemanding nature documentary matched in duration to the mental-fatigue protocols, serving as a non-fatiguing control condition.
实验性的:MF10 (10-min Mental Fatigue)
Participants performed the Stroop color-word task continuously for 10 minutes to induce mental fatigue.
Continuous performance of the Stroop color-word interference task for 10 minutes to induce mental fatigue.
实验性的:MF15 (15-min Mental Fatigue)
Participants performed the Stroop color-word task continuously for 15 minutes to induce mental fatigue.
Continuous performance of the Stroop color-word interference task for 15 minutes to induce mental fatigue.
实验性的:MF30 (30-min Mental Fatigue)
Participants performed the Stroop color-word task continuously for 30 minutes to induce mental fatigue.
Continuous performance of the Stroop color-word interference task for 30 minutes to induce mental fatigue.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Countermovement Jump (CMJ) Height
大体时间:Immediately after completion of each experimental protocol (control, and 10-, 15-, and 30-minute Stroop-task mental fatigue conditions); sessions were separated by a minimum 72-hour washout period.
Countermovement jump (CMJ) height was assessed using the My Jump Lab application (version 5.2; C. Balsalobre-Fernández, Madrid, Spain) via video recorded at 240 frames/s on an iPad Air 11-inch (M3), positioned on a tripod approximately 2 m from the participant. Take-off and landing frames were identified manually by the same investigator using the application's frame-by-frame function, and jump height was calculated from flight time using the equation h = (g·t²)/8. Two jump attempts were performed in each experimental session, with 60 seconds of rest between trials, and the better performance was retained for analysis.
Immediately after completion of each experimental protocol (control, and 10-, 15-, and 30-minute Stroop-task mental fatigue conditions); sessions were separated by a minimum 72-hour washout period.

次要结果测量

结果测量
措施说明
大体时间
Countermovement Jump-Derived Mechanical and Kinematic Parameters
大体时间:Immediately after completion of each experimental protocol.
Countermovement jump (CMJ)-derived mechanical and kinematic parameters were obtained using the My Jump Lab application from the CMJ assessment performed at the end of each experimental protocol. Average velocity (m/s), take-off velocity (m/s), and impulse (N·s) were provided automatically by the application as derived sub-parameters, computed from jump height and body mass using the biomechanical model incorporated in My Jump Lab. Flight time (ms) was calculated from the same video recording using the application's frame-by-frame analysis. These parameters were analyzed as complementary derived measures of CMJ performance.
Immediately after completion of each experimental protocol.
EEG Absolute Band Power (Delta, Theta, Alpha, Beta)
大体时间:Recorded immediately before and immediately after each experimental protocol (control, and 10-, 15-, and 30-minute Stroop-task mental fatigue conditions); each recording lasted 3 minutes with eyes closed.
Resting-state EEG was recorded using a 10-electrode montage (Fp1, Fp2, Fz, FC1, FC2, Cz, Pz, O1, Oz, O2) following the international 10-20 system, via a wireless EEG system (Emotiv EPOC Flex) sampling at 256 Hz. Following preprocessing (0.5-45 Hz band-pass filtering, ICA-based artifact removal, and amplitude normalization), power spectral density was computed for each channel using Welch's method, and absolute power was calculated within the delta (1-4 Hz), theta (4-8 Hz), alpha (8-13 Hz), and beta (13-30 Hz) frequency bands, expressed in normalized (dimensionless) units.
Recorded immediately before and immediately after each experimental protocol (control, and 10-, 15-, and 30-minute Stroop-task mental fatigue conditions); each recording lasted 3 minutes with eyes closed.
EEG Theta/Beta Ratio
大体时间:Immediately before and immediately after each experimental protocol.
The theta-to-beta power ratio was calculated from resting-state EEG recordings (10-electrode montage, international 10-20 system) by dividing theta-band power by beta-band power for each channel. The outcome was expressed as a unitless ratio.
Immediately before and immediately after each experimental protocol.
EEG Spectral Entropy
大体时间:Immediately before and immediately after each experimental protocol.
Spectral entropy was computed from the resting-state EEG power spectrum of each channel as a measure of signal complexity, used to characterize the transition from an alert to a fatigued cortical state.
Immediately before and immediately after each experimental protocol.
EEG Sample Entropy
大体时间:Immediately before and immediately after each experimental protocol.
Sample entropy was computed from the resting-state EEG time series of each channel as a nonlinear measure of signal irregularity and complexity.
Immediately before and immediately after each experimental protocol.
Frontal Theta Power
大体时间:Immediately before and immediately after each experimental protocol.
Frontal theta power was extracted from frontal electrode sites (Fp1, Fp2, Fz) as a regional marker of cognitive-control demand and effortful attentional monitoring.
Immediately before and immediately after each experimental protocol.
Posterior Alpha Power
大体时间:Immediately before and immediately after each experimental protocol.
Posterior alpha power was extracted from occipital electrode sites (O1, Oz, O2) as a regional marker of cortical inhibition and fatigue-related attentional state.
Immediately before and immediately after each experimental protocol.
Subjective Mental Fatigue (VAS Score)
大体时间:Immediately before and immediately after each experimental protocol.
Subjective mental fatigue was rated using a paper-based 0-10 visual analogue scale, anchored at 0 ("not mentally fatigued at all") and 10 ("the highest possible level of mental fatigue"), in response to the question "How mentally fatigued do you feel right now?" Prior ratings were not visible when a new rating was provided.
Immediately before and immediately after each experimental protocol.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年5月1日

初级完成 (实际的)

2026年7月1日

研究完成 (实际的)

2026年8月1日

研究注册日期

首次提交

2026年8月4日

首先提交符合 QC 标准的

2026年8月4日

首次发布 (实际的)

2026年8月10日

研究记录更新

最后更新发布 (实际的)

2026年8月10日

上次提交的符合 QC 标准的更新

2026年8月4日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • INU-2025-8104-MFCMJ
  • 2025/8104 (其他标识符:İnönü University Non-Interventional Clinical Research Ethics Committee)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data will not be shared because the study includes a small sample size, and no data-sharing plan was included in the approved study protocol or informed consent. Aggregate study results will be reported in scientific publications.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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