Caffeine Clinical Trial
Official title:
Neurophysiological Reserve: Peripheral and Central Effects of Caffeine Manipulation
The objective of this study is to verify if there is a neurophysiologic reserve when caffeine and placebo perceived as caffeine are manipulated in closed- and opened-loop exercises. Parameters of excitability level of skeletal muscle and Central Nervous System (CNS), and peripheral metabolism will be measured
A neurophysiological reserve related to central mechanisms is supposed to be present, which
should be observed when an increased central drive occurs. In theory, according to the
central regulation model of effort, an increased performance could be due to the elevation
on Central Nervous System excitability and activity, since exercise is not peripherally
limited. Conversely, the absence of muscle performance improvement to the increased central
drive promoted by caffeine would be an evidence for a peripherally localized
neurophysiological limit and would indicate the absence of reserve. Therefore, if present,
this reserve could be verified by using peripheral and central measures derived from
electric-stimulation, evoked twitch and interpolated twitch techniques, associated to
measures of EMG and peripheral metabolism, when caffeine is manipulated during closed- and
opened-loop exercise.
In addition, there should also be possible to access the reserve without stimulant substance
manipulation (placebo effect). By teleological argument derived from the central regulation
model of effort, a neurophysiological reserve would be a natural mechanism to protect the
cellular integrity. Therefore, it would be reasonable to hypothesize that, if present, a
reserve would be observed by an increase in performance promoted by an elevation in central
drive when placebo is perceived as caffeine. Unfortunately, however, no study utilized this
experimental approach, including measures of central and peripheral activity during closed-
and opened-loop exercise, to consistently respond the reserve question.
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Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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