Running kinematics and shock absorption do not change after brief exhaustive running.

Published

Journal Article

Because of the nature of running, the forces encountered require a proper coordination of joint action of the lower extremity to dissipate the ground reaction forces and accelerations through the kinetic chain. Running-related muscle fatigue may reduce the shock absorbing capacity of the lower extremity and alter running kinematics. The purpose of this study was to determine if a bout of exhaustive running at a physiologically determined high intensity, changes running kinematics, impact accelerations, and alters shock attenuating capabilities. It was hypothesized that as a result of fatigue induced by an exhaustive run, running kinematics, impact accelerations at the head and shank, acceleration reduction, and shock attenuation would change. A within-subject, repeated-measures design was used for this study. Twelve healthy, competitive male and female distance runners participated. Subjects performed 2 testing sessions consisting of a VO2max treadmill protocol to determine the heart rate at ventilatory threshold and a fatigue-inducing running bout at the identified ventilatory threshold heart rate. Kinematic data included knee flexion, pronation, time to maximum knee flexion, and time to maximum pronation. Acceleration data included shank acceleration, head acceleration, and shock attenuation. No significant differences resulted for the kinematic or acceleration variables. Although the results of this study do not support the original hypotheses, the influence of running fatigue on kinematics and accelerations remains inconclusive. Future research is necessary to examine fatigue-induced changes in running kinematics and accelerations and to determine the threshold at which point the changes may occur.

Full Text

Duke Authors

Cited Authors

  • Abt, JP; Sell, TC; Chu, Y; Lovalekar, M; Burdett, RG; Lephart, SM

Published Date

  • June 2011

Published In

Volume / Issue

  • 25 / 6

Start / End Page

  • 1479 - 1485

PubMed ID

  • 21386724

Pubmed Central ID

  • 21386724

Electronic International Standard Serial Number (EISSN)

  • 1533-4287

Digital Object Identifier (DOI)

  • 10.1519/JSC.0b013e3181ddfcf8

Language

  • eng

Conference Location

  • United States