Mindfulness, Mental Fatigue, Inhibitory Control and Endurance Performance in Athletes
Primary Purpose
Mental Fatigue
Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Mental fatigue condition
Control condition
Sponsored by
About this trial
This is an interventional screening trial for Mental Fatigue focused on measuring Mindfulness, Athletes, Mental fatigue, Inhibitory control, Endurance performance
Eligibility Criteria
Inclusion Criteria:
- Regular sports training at least 4 hours weekly
- Normal or corrected-to-normal vision
- Right-handed
Exclusion Criteria:
- Physical limitation or injury in lower limbs before and during the study
- Diagnosed or self-reported neurological disorders (e.g., epilepsy)
- Diagnosed or self-reported major psychiatric illness (e.g., major depression, schizophrenia)
Sites / Locations
- Department of Physical Education and Sport Sciences, National Taiwan Normal University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Mental fatigue condition
Control condition
Arm Description
Performing a completed incongruent version of Stroop task for 30min.
Performing a completed congruent version of Stroop task for 30min.
Outcomes
Primary Outcome Measures
Inhibitory control: Reaction time
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).
Inhibitory control: Accuracy
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).
Endurance performance: Time to exhaustion
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.
Endurance performance: Maximum Oxygen Consumption
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.
Changes in neuroelectrical activities
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
Subjective mental fatigue
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).
Objective mental fatigue: Reaction time in Stroop task
During the intervention, the reaction time in both Stroop tasks will be calculated as an index of objective mental fatigue.
Objective mental fatigue: Accuracy in Stroop task
During the intervention, the accuracy in both Stroop tasks will be calculated as an index of objective mental fatigue.
Rating of perceived exertion
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.
Full Information
NCT ID
NCT05466136
First Posted
July 6, 2022
Last Updated
June 3, 2023
Sponsor
National Taiwan Normal University
1. Study Identification
Unique Protocol Identification Number
NCT05466136
Brief Title
Mindfulness, Mental Fatigue, Inhibitory Control and Endurance Performance in Athletes
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
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
April 20, 2022 (Actual)
Primary Completion Date
October 31, 2022 (Actual)
Study Completion Date
October 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan Normal University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. 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.
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).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mental Fatigue
Keywords
Mindfulness, Athletes, Mental fatigue, Inhibitory control, Endurance performance
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Mental fatigue condition
Arm Type
Experimental
Arm Description
Performing a completed incongruent version of Stroop task for 30min.
Arm Title
Control condition
Arm Type
Experimental
Arm Description
Performing a completed congruent version of Stroop task for 30min.
Intervention Type
Behavioral
Intervention Name(s)
Mental fatigue condition
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Control condition
Intervention Description
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.
Primary Outcome Measure Information:
Title
Inhibitory control: Reaction time
Description
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).
Time Frame
about 1 year
Title
Inhibitory control: Accuracy
Description
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).
Time Frame
about 1 year
Title
Endurance performance: Time to exhaustion
Description
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.
Time Frame
about 1 year
Title
Endurance performance: Maximum Oxygen Consumption
Description
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.
Time Frame
about 1 year
Title
Changes in neuroelectrical activities
Description
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.
Time Frame
about 1 year
Secondary Outcome Measure Information:
Title
Subjective mental fatigue
Description
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).
Time Frame
about 1 year
Title
Objective mental fatigue: Reaction time in Stroop task
Description
During the intervention, the reaction time in both Stroop tasks will be calculated as an index of objective mental fatigue.
Time Frame
about 1 year
Title
Objective mental fatigue: Accuracy in Stroop task
Description
During the intervention, the accuracy in both Stroop tasks will be calculated as an index of objective mental fatigue.
Time Frame
about 1 year
Title
Rating of perceived exertion
Description
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.
Time Frame
about 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Regular sports training at least 4 hours weekly
Normal or corrected-to-normal vision
Right-handed
Exclusion Criteria:
Physical limitation or injury in lower limbs before and during the study
Diagnosed or self-reported neurological disorders (e.g., epilepsy)
Diagnosed or self-reported major psychiatric illness (e.g., major depression, schizophrenia)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yu-Kai Chang, Ph.D
Organizational Affiliation
Department of Physical Education and Sport Sciences, National Taiwan Normal University
Official's Role
Study Director
Facility Information:
Facility Name
Department of Physical Education and Sport Sciences, National Taiwan Normal University
City
Taipei
ZIP/Postal Code
106
Country
Taiwan
12. IPD Sharing Statement
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Mindfulness, Mental Fatigue, Inhibitory Control and Endurance Performance in Athletes
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