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Clinical Trial Summary

The current study will add to the current knowledge by combining several electrophysiological techniques to examine the relationship between physiological responses and cognitive fatigue and daily activity performance in a stress- and fatigue-inducing protocol. The aims of this study are: 1) to evaluate the feasibility and usability of assessing physiological responses in an experimental set-up and 2) to investigate the association between physiological outcomes, experimentally induced stress and cognitive fatigue in people with multiple sclerosis (MS) and healthy controls.


Clinical Trial Description

In an experimental set-up participants (20 people with MS and 20 healthy controls) will perform a high-challenging cognitive protocol to provoke stress and (cognitive) fatigue. Physiological responses (heart rate variability, skin conductance, body temperature) and brain activity (EEG) will be measured while resting (resting baseline), while speaking as normal (speaking baseline), during protocol performance and following the protocol (post-protocol). Demographic and clinical characteristics, as well as levels of perceived fatigue, stress, pain, daily activity performance, quality of life and anxiety and depression will be assessed using medical records and questionnaires. Feasibility and usability will be assessed in participants and researcher(s) by standardized questionnaires. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05003375
Study type Observational
Source KU Leuven
Contact Daphne Kos, PhD
Phone +32496-107849
Email daphne.kos@kuleuven.be
Status Recruiting
Phase
Start date October 15, 2020
Completion date September 1, 2021

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