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Cause and Consequence of Neural Fatigue

Cause and Consequence of Neural Fatigue

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02721745
Acronym
Fatstim
Enrollment
216
Registered
2016-03-29
Start date
2016-05-23
Completion date
2020-12-31
Last updated
2021-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Fatigue

Brief summary

While the scientific community understands quite well why muscles ache after prolonged exercise, the origins of mental fatigue remain totally mysterious. Existing theories remain at a psychological level, with scarce supporting evidence. Mental fatigue typically occurs after long episodes during which humans exert control on motor or cognitive processes, instead of executing routine or stimulus-driven behaviours. However, work organization (especially in risky job like airplane control or medical profession) and pathologies due to an overload of work (like burn-out) seems to be directly linked to neural fatigue. One of the consequences of neural fatigue is to alter decision-making. As an example, the choice between an immediate monetary reward and a larger but delayed monetary reward (the so called intertemporal choices) are susceptible to fatigue state of its underpinning neural network. The investigators are proposing an exploratory study of neural fatigue, induced either in a natural way (by performing cognitive tasks for hours) or by transcranial stimulation, using three main physiological measures (Electro-encephalography to measure neural activity, indirect calorimetry to measure the metabolic cost of a cognitive effort, and pupillometry to measure cognitive effort). This study should allow to better understand the consequences of neural fatigue on cognitive functions like decision making as well as the associated physiological variables.

Interventions

BEHAVIORALNatural Fatigue

Experimental: EEG Indirect Calorimetry Pupillometry

DEVICEtDCS

Experimental: EEG Indirect Calorimetry Pupillometry

DEVICETMS

Experimental: EEG Indirect Calorimetry Pupillometry

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 39 Years
Healthy volunteers
Yes

Inclusion criteria

* Right-handed people; * between 20 à 39 years old; * able to understand the instructions and to perform the behavioral tasks of the study ; * informed consent to take part to the study (signature of a a consent form); * people being registered to social security or universal medical protection or equivalent;

Exclusion criteria

For each experiment: * neurological, psychiatric or serious illness history * ongoing or recently stopped (lower than three weeks) psychotropic treatment; * excessive psychotropic substances consumption or chronical consumption the examination day; * People being not able to perform the tasks (alteration of one of the cognitive functions or elementary visual disorder avoiding the identification of the experimental stimuli); * adult under legal protection (guardianship, or under the protection of a conservator); * adult people being not able to express his consent; * people being deprived of liberty as a consequence of an administrative or judicial decision; * pregnant, parturient or nursing women; * people taking part to another biomedical study or still being in the exclusion phase of another research; * hospitalized people without consent; * people who could not participate to the full study for any reasons. For the experiments involving transcranial stimulation, in addition to the previous ones: * take of drugs known to lower the epileptogenic threshold; * take of barbiturate, gabapentin, topiramate, clonazepam in the 7 days before the first visit; * history of awareness loss; * people having contraindication for having a transcranial magnetic stimulation or for having an MRI examination; * People who does not want to be informed of any significant irregularity that could be detected during the MRI examination; * claustrophobic people ;

Design outcomes

Primary

MeasureTime frameDescription
Proportion of chosen immediate reward in intertemporal questions between an immediate reward smaller than a delayed reward.Day 0Several questions between two options (an immediate reward and and a larger delayed reward) will be asked to the participants through a computer. The measure of impulsivity corresponds to the proportion of immediate reward that wil be chosen through the keyboard (left or right arrows).
Physiological Measures: EEGDay 0power of electrical brain oscillation.
Physiological Measures: indirect calorimetryday 0volume of O2 consumption and CO2 expulsion.
Physiological Measures:pupillometryDay 0pupil dilation.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026