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

Sponsor
National Taiwan Normal University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05466136
Collaborator
(none)
90
1
2
8.7
10.3

Study Details

Study Description

Brief Summary

This study investigated the mediating effect of dispositional mindfulness on the impact of mental fatigue on neurocognitive functions and endurance performance in athletes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mental fatigue condition
  • Behavioral: Control condition
N/A

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) and Athlete Mindfulness Questionnaire (AMQ), respectively.

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 Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
The participants will visit the lab on two counterbalanced order occasions to complete either an incongruent version Stroop task (mental fatigue condition, MF) or a congruent version Stroop task (control condition, CON) for 30 minutes to induce the mental fatigue state.The participants will visit the lab on two counterbalanced order occasions to complete either an incongruent version Stroop task (mental fatigue condition, MF) or a congruent version Stroop task (control condition, CON) for 30 minutes to induce the mental fatigue state.
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
Effects of Mental Fatigue on Inhibitory Control and Endurance Performance in Athletes With Different Levels of Dispositional Mindfulness: An Event-Related Potential Study
Actual Study Start Date :
Apr 20, 2022
Anticipated Primary Completion Date :
Oct 31, 2022
Anticipated Study Completion Date :
Jan 10, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mental fatigue condition

Performing a completed incongruent version of Stroop task for 30min.

Behavioral: Mental fatigue 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

Performing a completed congruent version of Stroop task for 30min.

Behavioral: Control 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.

Outcome Measures

Primary Outcome Measures

  1. Inhibitory control: Reaction time [about 1 year]

    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 will be presented with five arrows and will be instructed to respond as quickly and accurately as possible to the direction where the middle arrow is pointing (i.e., left or right).

  2. Inhibitory control: Accuracy [about 1 year]

    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 will be presented with five arrows and will be instructed to respond as quickly and accurately as possible to the direction where the middle arrow is pointing (i.e., left or right).

  3. Endurance performance: Time to exhaustion [about 1 year]

    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.

  4. Endurance performance: Maximum Oxygen Consumption [about 1 year]

    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.

  5. Changes in neuroelectrical activities [about 1 year]

    The neuroelectrical activities during the computerized cognitive tasks (i.e., Stroop task & Flanker task) will be recorded. The changes in the event-related potential (e.g., P3) will be analyzed.

Secondary Outcome Measures

  1. Subjective mental fatigue [about 1 year]

    Before, after Stroop task, and after Flanker task, changes in subjective mental fatigue will be measured using a visual analog scale for mental fatigue (VAS-MF). Participants will be 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).

  2. Objective mental fatigue: Reaction time in Stroop task [about 1 year]

    During the intervention, the reaction time in both Stroop tasks will be calculated as an index of objective mental fatigue.

  3. Objective mental fatigue: Accuracy in Stroop task [about 1 year]

    During the intervention, the accuracy in both Stroop tasks will be calculated as an index of objective mental fatigue.

  4. Rating of perceived exertion [about 1 year]

    The Rating of perceived exertion (RPE) will be measured at beginning and every 2.5-min during the GXT using Borg 6 to 20 scale, until the participant comes to voluntary exhaustion.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Physical Education and Sport Sciences, National Taiwan Normal University Taipei Taiwan 106

Sponsors and Collaborators

  • National Taiwan Normal University

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Taiwan Normal University
ClinicalTrials.gov Identifier:
NCT05466136
Other Study ID Numbers:
  • PACNL_JT_MF_Trait
First Posted:
Jul 20, 2022
Last Update Posted:
Jul 20, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by National Taiwan Normal University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 20, 2022