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Design of an Eccentric Recumbent Ergometer to Elicit Delayed Onset Muscle Soreness

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Introduction: Our objective was to design an eccentric bicycle design to elicit delayed onset muscle soreness (DOMS). Methods: To assess the bicycle designs’ ability to elicit DOMS, fourteen, recreationally active, males performed five-minutes of eccentric bicycling at 50% of their individualized power determined from a modified six-second Wingate test. Outcome measures to assess DOMS included the Likert pain scale, creatine kinase, lactate blood concentration, and pressure algometry detection evaluated at four time points (baseline (before the eccentric bicycling), immediate post, 24 hours post, and 48 hours post). Results: The Likert pain scale was different (F = 75.88, p < 0.001) at baseline (0.14 ± 0.36) and immediate post (0.21 ± 0.43), compared to 24 hours post (3.07 ± 0.83), and 48 hours post (2.93 ± 1.07). No changes were reported for creatine kinase (F = 0.7167, p = 0.475), lactate blood concentration (F = 2.313, p = 0.107), or pressure algometry detection. Conclusions: To understand mechanisms of DOMS, there is a need for a consistent, reliable method for producing DOMS. Our eccentric bicycle design and protocol offers an alternative approach to previous eccentric ergometer designs - demonstrating the potential to elicit DOMS in one, five-minute session.
Title: Design of an Eccentric Recumbent Ergometer to Elicit Delayed Onset Muscle Soreness
Description:
Introduction: Our objective was to design an eccentric bicycle design to elicit delayed onset muscle soreness (DOMS).
Methods: To assess the bicycle designs’ ability to elicit DOMS, fourteen, recreationally active, males performed five-minutes of eccentric bicycling at 50% of their individualized power determined from a modified six-second Wingate test.
Outcome measures to assess DOMS included the Likert pain scale, creatine kinase, lactate blood concentration, and pressure algometry detection evaluated at four time points (baseline (before the eccentric bicycling), immediate post, 24 hours post, and 48 hours post).
Results: The Likert pain scale was different (F = 75.
88, p < 0.
001) at baseline (0.
14 ± 0.
36) and immediate post (0.
21 ± 0.
43), compared to 24 hours post (3.
07 ± 0.
83), and 48 hours post (2.
93 ± 1.
07).
No changes were reported for creatine kinase (F = 0.
7167, p = 0.
475), lactate blood concentration (F = 2.
313, p = 0.
107), or pressure algometry detection.
Conclusions: To understand mechanisms of DOMS, there is a need for a consistent, reliable method for producing DOMS.
Our eccentric bicycle design and protocol offers an alternative approach to previous eccentric ergometer designs - demonstrating the potential to elicit DOMS in one, five-minute session.

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