The Individual Response of Healthy Individuals to Mental Fatigue

Status Recruiting

Clinical Trial Summary

The objective of the present study is to confirm and map out the presence of interindividual differences in the effect of mental fatigue on both physical and cognitive performance, and to see if these differences are related to individual factors of the participants.

Clinical Trial Description

Every participant will visit the lab a total of three times within a period of two weeks. In the first visit, they will undergo both a detailed screening as well as perform all intervention/control trial measures to familiarize themselves with the utilised equipment. This detailed screening entails, among other things, a maximal incremental exercise test, a cognitive test battery and multiple subjective questionnaires. The experimental and control trial are almost identical, with the only difference being the task performed in the middel of the trial. At the beginning of the trial the EEG will be fitted to the head of the participant and baseline measures will be taken. Afterwards, participants will perform a go nogo task to assess baseline cognitive performance. Then the intervention (i.e. Stroop task) or control (i.e. documentary) task will be performed. The goal of the Stroop task is to elicit mental fatigue, while the documentary provides a meaningful comparison. Afterwards, cognitive performance will again be assessed using the go no go task, followed by a physical performance task in the form of a time trial. The different internal factors assessed during the screening stage will be correlated to the difference in cognitive and physical performance between the intervention and control trial. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05576935
Study type	Interventional
Source	Vrije Universiteit Brussel
Contact	Bart Roelands, PhD
Phone	02/629.22.22
Email	bart.roelands@vub.be
Status	Recruiting
Phase	N/A
Start date	July 1, 2022
Completion date	December 31, 2024

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