Mindfulness, Mental Fatigue, Inhibitory Control and Endurance Performance in Athletes

March 13, 2026 updated by: National Taiwan Normal University

Effects of Mental Fatigue on Inhibitory Control and Endurance Performance in Athletes With Different Levels of Dispositional Mindfulness: An Event-Related Potential Study

This study investigated whether trait mindfulness in athletes is associated with impairments in neurocognitive function and endurance performance resulting from mental fatigue.

Study Overview

Detailed Description

Recent research suggests that mental fatigue by prolonged cognitive tasks would impair neurocognitive functions (e.g., executive functions, brain activity) and sports performance, especially inhibitory control and endurance performance. On the other hand, individuals with higher dispositional mindfulness have been linked to greater athletic performance and cognitive functions. Still, there is little known whether higher dispositional mindfulness counteracts the detrimental effects of mental fatigue on endurance performance and inhibitory control in athletes. Therefore, this study is conducted to investigate whether dispositional mindfulness mediates the effects of mental fatigue on neurocognitive functions and endurance performance in athletes.

The qualified participants will visit the lab on two counterbalanced order occasions to complete either a modified incongruent Stroop task (mental fatigue condition, MF) or a modified congruent Stroop task (control condition, CON) for 30 minutes. Before and after each cognitive task, participants will be measured for their subjective mental fatigue by a visual analog scale (VAS). After each cognitive task, inhibitory control and endurance performance will be evaluated by a Flanker task and a graded exercise test (GXT), respectively. Furthermore, the general and athletic dispositional mindfulness will be measured using the Five Facet Mindfulness Questionnaire (FFMQ).

Specifically, the targeted primary outcomes are neurocognitive functions (i.e., reaction time, accuracy and ERPs in Flanker task) and endurance performance (i.e., VO2max & time to exhaustion in GXT); The secondary outcomes are subjective (i.e., VAS score)/objective (i.e., reaction time, accuracy in Stroop task) mental fatigue, motivation in tasks, mood (i.e., BRUMS-C).

Study Type

Interventional

Enrollment (Actual)

90

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan, 106
        • Department of Physical Education and Sport Sciences, National Taiwan Normal University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 25 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Regular sports training at least 4 hours weekly
  2. Normal or corrected-to-normal vision
  3. Right-handed

Exclusion Criteria:

  1. Physical limitation or injury in lower limbs before and during the study
  2. Diagnosed or self-reported neurological disorders (e.g., epilepsy)
  3. Diagnosed or self-reported major psychiatric illness (e.g., major depression, schizophrenia)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Screening
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Mental Fatigue Condition, Then Control Condition
Performing a completed incongruent version of Stroop task for 30min in mental fatigue condition. Then performing a completed congruent version of Stroop task for 30min in control condition.
In mental fatigue condition, the mental fatigue manipulation will use a modified Stroop task with complete incongruent trials, which is wildly used to induce a mentally fatigued state in previous studies. The Stroop task included four colored words presented in traditional Chinese (i.e., red, green, blue, and yellow), the color of the word will paint inconsistent with the semantic meaning of the word (e.g., red word printed in green). The task consisted of five 6-minute blocks and 1080 incongruent trials for each block. The total duration will be 30-min.
Experimental: Control Condition, Then Mental Fatigue Condition
Performing a completed congruent version of Stroop task for 30min in Control condition. Then performing a completed incongruent version of Stroop task for 30min in mental fatigue condition.
Similar to mental fatigue conditions, the modified Stroop task with complete congruent trials will be used, The Stroop task also included four colored words presented in traditional Chinese (i.e., red, green, blue, and yellow), but the color of the word will paint consistent with the semantic meaning of the word (e.g., red word printed in red) in order to set up the match condition of relative less cognitive demanding for participants. Same with the mental fatigue condition, the task consisted of five 6-minute blocks and 1080 congruent trials for each block. The total duration will be 30-min.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Inhibitory Control: Reaction Time
Time Frame: From enrollment to the end of second intervention at 1 week. During Flanker task, up to 15 minutes.
Inhibitory control will be evaluated by a Flanker task in terms of reaction time in this study, and the types of trials are the congruent (i.e., > > > > >) and incongruent (i.e., < < > < <). In the Flanker task, participants were presented with five arrows and instructed to respond as quickly and accurately as possible to the direction where the middle arrow is pointing (i.e., left or right).
From enrollment to the end of second intervention at 1 week. During Flanker task, up to 15 minutes.
Inhibitory Control: Accuracy
Time Frame: From enrollment to the end of second intervention at 1 week. During Flanker task, up to 15 minutes.
Inhibitory control will be evaluated by a Flanker task in terms of accuracy in this study, and the types of trials are the congruent (i.e., > > > > >) and incongruent (i.e., < < > < <). In the Flanker task, participants were presented with five arrows and instructed to respond as quickly and accurately as possible to the direction where the middle arrow is pointing (i.e., left or right).
From enrollment to the end of second intervention at 1 week. During Flanker task, up to 15 minutes.
Endurance Performance: Time to Exhaustion
Time Frame: From enrollment to the end of second intervention at 1 week. During graded exercise test, up to 30 minutes
The endurance performance in terms of time to exhaustion (TTE) will be assessed by graded exercise test (GXT) with Bruce protocol on treadmill (h/p/cosmos pulsar 3p, Germany). The initial speed and grade of the GXT will be set at 2.74 km/hr with grade of 10% and increase speed and grade every 3 min until participants are volitionally exhausted.
From enrollment to the end of second intervention at 1 week. During graded exercise test, up to 30 minutes
Endurance Performance: Maximum Oxygen Consumption
Time Frame: From enrollment to the end of second intervention at 1 week. During graded exercise test, up to 30 minutes.
The maximal oxygen consumption (VO2max) throughout the whole GXT will be recorded by a computerized indirect calorimetry system (SensorMedics Vmax 29C, USA), and until the participants reached volitional exhaustion. The VO2max in the study will be defined as the highest 30-s average value of VO2 measured during GXT.
From enrollment to the end of second intervention at 1 week. During graded exercise test, up to 30 minutes.
Changes in Neuroelectrical Activities
Time Frame: From enrollment to the end of second intervention at 1 week. During Flanker task, up to 15 minutes.
Neuroelectrical activity during the Flanker task was recorded using electroencephalography (EEG) with continuous data acquisition throughout task performance. Changes in neuroelectrical activity were operationalized as differences in event-related potential (ERP) amplitudes during the Flanker task (e.g., N2 and P3 components). The mean amplitudes of the N2 and P3 were quantified within predefined time windows of 250-350 ms and 350-550 ms, respectively, following stimulus onset.
From enrollment to the end of second intervention at 1 week. During Flanker task, up to 15 minutes.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Subjective Mental Fatigue
Time Frame: Three standardized time points within each experimental session at baseline and post-intervention: T0 (before the Stroop task), T1 (after the Stroop task), and T2 (after the Flanker task).
Before, after Stroop task, and after Flanker task, changes in subjective mental fatigue was measured using a visual analog scale for mental fatigue (VAS-MF). Participants were asked the following questions "What is your mental fatigue level now?", and participants could indicate how mental fatigue on a scale from 0 (i.e., no mental fatigue at all) to 100 (i.e., completely mentally exhausted).
Three standardized time points within each experimental session at baseline and post-intervention: T0 (before the Stroop task), T1 (after the Stroop task), and T2 (after the Flanker task).
Objective Mental Fatigue: Reaction Time in Stroop Task
Time Frame: From enrollment to the end of second intervention at 1 week. During Stroop task, up to 30 minutes.
During the intervention, the reaction time in both Stroop tasks was calculated as an index of objective mental fatigue.
From enrollment to the end of second intervention at 1 week. During Stroop task, up to 30 minutes.
Objective Mental Fatigue: Accuracy in Stroop Task
Time Frame: From enrollment to the end of second intervention at 1 week. During Stroop task, up to 30 minutes.
During the intervention, the accuracy in both Stroop tasks was calculated as an index of objective mental fatigue.
From enrollment to the end of second intervention at 1 week. During Stroop task, up to 30 minutes.
Mood State
Time Frame: Two standardized time points within each experimental session at baseline and post-intervention: T0 (before the Stroop task) and T1 (after the Stroop task).

Mood state was determined by the difference in scores on the Brunel Mood Scale-Chinese (BRUMS-C) between before (i.e., T0) and after (i.e., T1) Stroop task.

The BRUMS-C consists of 23 items rated on a 5-point Likert scale and comprises six subscales: anger, confusion, depression, tension, fatigue, and vigor. Each subscale score is calculated as the mean of its corresponding items, with possible scores ranging from 0 to 4. Higher mean scores indicate greater intensity of the respective mood state.

Two standardized time points within each experimental session at baseline and post-intervention: T0 (before the Stroop task) and T1 (after the Stroop task).
Motivation
Time Frame: From enrollment to the end of second intervention at 1 week. Immediately after completing Flanker task and GXT.
The level of effort exerted by participants during the Flanker task and GXT was assessed using the VAS for motivation (VAS-M). Immediately after completing each task, participants were also asked to mark a 100mm line to rate their motivation to perform at their best (i.e., "How motivated are you to perform to the best of your ability in the task?") on a scale ranging from 0, indicating "not at all," to 100, indicating "extremely motivated."
From enrollment to the end of second intervention at 1 week. Immediately after completing Flanker task and GXT.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Yu-Kai Chang, Ph.D, Department of Physical Education and Sport Sciences, National Taiwan Normal University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 20, 2022

Primary Completion (Actual)

October 31, 2022

Study Completion (Actual)

October 31, 2022

Study Registration Dates

First Submitted

July 6, 2022

First Submitted That Met QC Criteria

July 17, 2022

First Posted (Actual)

July 20, 2022

Study Record Updates

Last Update Posted (Actual)

March 16, 2026

Last Update Submitted That Met QC Criteria

March 13, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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