Study Objectives: The Psychomotor Vigilance Task (PVT) is widely recognized as the gold standard for measuring vigilance, providing a rapid and objective measure of this state. While driving simulations are also used, they typically require longer administration times. This study examines the sensitivity of driving simulation variables to sleep deprivation throughout the task. The aim is to determine the shorter duration at which performance declines can be observed. A secondary goal is to compare driving simulation and PVT variables' sensitivity in detecting sleep deprivation.
Methods: 43 participants (22 males; aged 46.7 ± 17.8 years) completed a 90-minute driving simulation and a 10-minute PVT under two conditions (normal sleep and partial sleep deprivation of 3.5 hours). Signed-rank Wilcoxon tests and effect sizes were computed for variables from both tasks. Effect sizes were calculated for each 10-minute interval to assess sensitivity over time.
Results: All the variables showed sensitivity to sleep deprivation. The largest effect sizes were observed in the driving simulation and specifically for the standard deviation of lateral position (SDLP) (r=0.73) and the standard deviation of steering wheel movement (SDSW) (r=0.73). A large effect size for the SDLP (r=0.71) was observed after only 20 minutes of driving. For the 10-minute PVT, the highest effect size was observed for the number of lapses (r=0.52).
Conclusion: Driving-related variables are highly sensitive to sleep deprivation while providing continuous performance measurements. The SDLP is a particularly sensitive variable even with a reduced driving time of 20 minutes, suggesting that driving simulation tasks can be effectively shortened to 20 minutes.
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http://dx.doi.org/10.1093/sleep/zsaf010 | DOI Listing |
Elife
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Institute for Quantum Computing and Department of Physics & Astronomy, University of Waterloo, 200 University Ave W, Waterloo, N2L 3G1 Ontario Canada.
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View Article and Find Full Text PDFFEBS Lett
January 2025
PHYLIFE, Physical Life Science, Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, Denmark.
5HTR is a G-protein-coupled receptor that drives many neuronal functions and is a target for psychedelic drugs. Understanding ligand interactions and conformational transitions is essential for developing effective pharmaceuticals, but mechanistic details of 5HTR activation remain poorly understood. We utilized all-atom molecular dynamics simulations and free-energy calculations to investigate 5HTR's conformational dynamics upon binding to serotonin and psilocin.
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