TY - JOUR
T1 - The influence of knowledge of performance endpoint on pacing strategies, perception of effort, and neural activity during 30-km cycling time trials
AU - Wingfield, Georgia
AU - Marino, Frank
AU - Skein, Melissa
N1 - Includes bibliographical references.
PY - 2018/11
Y1 - 2018/11
N2 - It is understood that withholding information during exercise can alter performance during self-paced exercise, though less is known about neural activity during such exercise. The aim of this study was to compare the effects of withholding versus providing distance feedback on perception, muscular activation, and cerebral activity during cycling time trials (TT). Nine well-trained male cyclists randomly completed 2 x 30-km TT, with provision of performance information and distance feedback (known; KTT), and without performance information and remaining distance (unknown; UTT). Prefrontal cortex (PFC) hemoglobin concentration, electroencephalogy (EEG) responses of the parietal lobe (PL) and motor cortex (MC), and surface electromyogram (EMG) of the right thigh were monitored throughout the TTs, in addition to heart rate (HR), rating of perceived exertion (RPE), and power output (PO). Time to completion was shorter for the KTT compared to UTT (51.04 ± 3.26 vs. 49.25 ± 3.57 min, P = 0.01). There were no differences evident for RPE between conditions (P > 0.50). However, during the final 2 km, the KTT presented higher PO (P ≤ 0.05), HR (P = 0.03) and MC, and PL EEG activity (d = 0.51–0.71) in addition to increased tissue hemoglobin index (nTHI) and oxygen extraction (HHb) (d = 0.55-0.65) compared to the UTT. In conclusion, when withholding information pertaining to remaining distance, performance was reduced due to the application of a conservative pacing strategy. In addition, the increase in HHb across the PFC was strongly correlated with PO (r = 0.790; P < 0.001) suggesting knowledge about remaining distance may increase activation across the PFC. Further, it appears that changes within the PFC may play a role in the regulation of cycling performance.
AB - It is understood that withholding information during exercise can alter performance during self-paced exercise, though less is known about neural activity during such exercise. The aim of this study was to compare the effects of withholding versus providing distance feedback on perception, muscular activation, and cerebral activity during cycling time trials (TT). Nine well-trained male cyclists randomly completed 2 x 30-km TT, with provision of performance information and distance feedback (known; KTT), and without performance information and remaining distance (unknown; UTT). Prefrontal cortex (PFC) hemoglobin concentration, electroencephalogy (EEG) responses of the parietal lobe (PL) and motor cortex (MC), and surface electromyogram (EMG) of the right thigh were monitored throughout the TTs, in addition to heart rate (HR), rating of perceived exertion (RPE), and power output (PO). Time to completion was shorter for the KTT compared to UTT (51.04 ± 3.26 vs. 49.25 ± 3.57 min, P = 0.01). There were no differences evident for RPE between conditions (P > 0.50). However, during the final 2 km, the KTT presented higher PO (P ≤ 0.05), HR (P = 0.03) and MC, and PL EEG activity (d = 0.51–0.71) in addition to increased tissue hemoglobin index (nTHI) and oxygen extraction (HHb) (d = 0.55-0.65) compared to the UTT. In conclusion, when withholding information pertaining to remaining distance, performance was reduced due to the application of a conservative pacing strategy. In addition, the increase in HHb across the PFC was strongly correlated with PO (r = 0.790; P < 0.001) suggesting knowledge about remaining distance may increase activation across the PFC. Further, it appears that changes within the PFC may play a role in the regulation of cycling performance.
KW - Central regulation
KW - Fatigue
KW - Pacing strategies
KW - Self-paced exercise
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UR - http://www.scopus.com/inward/citedby.url?scp=85056514487&partnerID=8YFLogxK
U2 - 10.14814/phy2.13892
DO - 10.14814/phy2.13892
M3 - Article
C2 - 30426727
AN - SCOPUS:85056514487
SN - 2051-817X
VL - 6
SP - 1
EP - 13
JO - Physiological Reports
JF - Physiological Reports
IS - 21
M1 - e13892
ER -