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Difference in Central Fatigue During Two Ultra-endurance Practices: Running vs. Cycling

Difference in Central Fatigue During Two Ultra-endurance Practices: Running vs. Cycling

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04511858
Acronym
FAT-CENTR
Enrollment
19
Registered
2020-08-13
Start date
2021-03-05
Completion date
2021-07-15
Last updated
2021-11-24

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

Conditions

Ultra-marathon Runners

Keywords

central fatigue, peripheral fatigue, ultra-endurance exercise, corticospinal excitability

Brief summary

The mechanisms contributing to muscle fatigue in extreme long-duration exercise bouts are poorly understood. Ultra-endurance exercise is an excellent model for the study of adaptive responses to extreme loads and stress and it is an especially useful model for documenting the origins of central fatigue. This protocol will compare fatigue during and after ultra-endurance exercise bouts that result in moderate lower-limb tissue damage (i.e. cycling) or significant damage (i.e. running). The results of this protocol will allow us to further understanding of the reasons for major central fatigue, i.e. within the central nervous system, in ultra-endurance.

Interventions

OTHERmaximum effort test on a cycloergometer

5 h test on cycloergometer

OTHERmaximum effort test on a treadmill

5 h test on treadmill

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Prospective study of physiopathology on subjects specializing in endurance and ultra-endurance: comparing running vs. cycling. Cross-over: each subject will carry out the 2 experimental conditions (running and cycling) according to a randomized order of passage, respecting a wash-out of 2 weeks.

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Specialist in endurance and ultra-endurance. in the 2 disciplines: running and cycling (triathletes, duathletes or trailers achieving at least 30% of their training volume in cycling), and having at least finished one long distance event in the last 2 years, * Affiliated or beneficiary of a social security scheme. * Signature of the consent form

Exclusion criteria

* Any subject who has been injured in the 3 months prior to the protocol * Anyone with chronic joint pathologies (e.g.: repetitive sprains, patellar or ligament problems). * Any subject with chronic or central neurological pathologies * Any subject with a contraindication to magnetic stimulation * Use of neuro-active substances likely to alter cortico-spinal excitability (hypnotics, antiepileptics, psychotropic drugs, muscle relaxants) on the study. * Contraindication to the application of a magnetic field: * Heart or respiratory insufficiency. * Subject with a cardiac pace maker. * Cardiac valve wear and serious cardiovascular diseases. * Presence of prosthetic material or ferromagnetic foreign bodies in the head. * Presence of cochlear implants or ocular prosthetic material. * History of neurosurgical interventions. * Neurological diseases that may affect brain structures and cognitive abilities (e.g., intracranial tumour, multiple sclerosis, history of stroke or traumatic brain injury). * History of comitiality, contralateral knee disease or musculoskeletal disease. * Any subject participating at the same time in another interventional experiment requiring physical exercise. * Any subject who has taken corticosteroids within 3 months (inhalation, infiltration or history of prolonged corticosteroid therapy). * Any subject under guardianship or curatorship

Design outcomes

Primary

MeasureTime frameDescription
Maximum level of voluntary activation of relative central fatigueBefore and immediately after 5h exercisemeasured in isometric mode of the knee extensors, between the value before and immediately after a 5-hour cycling or running event at the same relative intensity

Secondary

MeasureTime frameDescription
Maximum level of voluntary activation of fatigue centrale absoluteBefore and immediately after 5h exercisemeasured in isometric mode of the knee extensors, between the value before the 5h cycling or running and the value after absolute exhaustion
Maximum level of voluntary activation with electrical evoked activationBefore and immediately after 5h exercisetests with measurement of the maximum voluntary with evoked electrical between the value before and immediately after a 5-hour cycling or running event at the same relative intensity
Spinal excitabilityBefore and immediately after 5h exercisethoracic spine stimulation for the recording of thoracic motor evoked potentials
Corticospinal excitabilityBefore and immediately after 5h exercisestimulation of the motor cortex for recording motor evoked potentials
Cortical excitabilityBefore and immediately after 5h exerciseratio between stimulation of the motor cortex and thoracic spine stimulation
Measurement of isometric force valuesBefore and immediately after 5h exercisesubjects sitting on a Cybex type seat, with the knee and hip angle set at 90°. The foot will be attached to a strain-gauge sensor using a velcro strap attached to the ankle above the medial malleolus.
Measurement of speed, force and power valuesBefore and immediately after 5h exerciseassessment of fatigue in dynamic mode (calculation of the force/speed profile)
Red blood cellsBefore and immediately after 5h exerciseblood sample
Measurement of the time maintained at the speed corresponding to the 2nd ventilatory thresholdBefore and immediately after 5h exerciseOn treadmill
White blood cellsBefore and immediately after 5h exerciseblood sample
HemoglobinBefore and immediately after 5h exerciseblood sample
Mean corpuscular hemoglobin concentrationBefore and immediately after 5h exerciseblood sample
C-reactive proteinBefore and immediately after 5h exerciseblood sample
Creatine PhosphoKinaseBefore and immediately after 5h exerciseblood sample
InterleukinesBefore and immediately after 5h exerciseblood sample
LactateBefore and immediately after 5h exerciseblood sample
measurement of the time maintained at the power corresponding to the 2nd ventilatory thresholdBefore and immediately after 5h exerciseOn Cycloergometer
PlateletsBefore and immediately after 5h exerciseblood sample

Countries

France

Outcome results

None listed

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