Does fatigue influence joint-specific work and ground force production during the first steps of maximal acceleration?

During initial acceleration, the first steps of a maximal-effort (sprint) run often determine success or failure in the capture and evasion of an opponent, and is therefore a vital factor of success in many modern sports. However, accelerative events are commonly performed after having already run considerable distances, and the associated fatigue should impair muscle force production and thus reduce acceleration. Despite this, the effects of running-induced fatigue on our ability to accelerate as well as the running technique used to achieve it have received little attention. We recorded 3-D kinematics and ground reaction forces during the first three steps of the acceleration phase from a standing start before and after performing a high-speed, multi-directional, fatiguing run-walk protocol in well-trained running athletes who were habituated to accelerative sprinting. We found that the athletes were able to maintain their acceleration despite changing running technique, which was associated with use of a more upright posture, longer ground contact time, increased vertical ground reaction impulse, decreased hip flexion and extension velocities, and a shift in peak joint moments, power, and positive work from the hip to the knee joint; no changes were detected in ankle joint function. Thus, a compensatory increase in knee joint function alleviated the reduction in hip flexor-extensor capacity. These acute adaptations may indicate that the hip extensors (gluteal and hamstring muscle groups) were more susceptible to fatigue than the ankle and knee musculature, and may thus be a primary target for interventions promoting fatigue resistance.

Neuromuscular fatigue and muscle damage following a simulated singles badminton match.

PURPOSE: To understand muscle damage in badminton, changes in neuromuscular function were investigated after simulated badminton singles matches performed by ten state-level male players. METHODS: Each participant played eight matches and measurements were taken before, immediately after, and 1 and 24 h after each match. Maximal voluntary isometric contraction (MVC) torque of the knee extensors and flexors, voluntary activation (VA) during MVC and torques generated by doublet (TDoublet), 20 (T20) and 80 Hz (T80) electrical stimulations of the knee extensors were measured from the dominant leg (the racket-hold arm side). Muscle soreness was assessed by a 100-mm visual analogue scale from both legs. The number of lunges performed by each participant in each match was analysed by videos, and its relations to other measures were examined. RESULTS: Pre-match knee extensor and flexor MVC torques were 278.4 ± 50.8 Nm and 143.0 ± 36.2 Nm, respectively. Knee extensor MVC torque of the dominant leg decreased immediately (12.0 ± 2.9%) and 1 h post-match (16.0 ± 3.2%), but returned to baseline at 24 h post-match. VA (11.4 ± 2.9%), TDoublet (13.1 ± 6.0%), T20 (31.1 ± 12.3%) and T80 (25.5 ± 7.9%) decreased (p < 0.01) immediately post-match but recovered by 24 h post-match. A significant correlation (r = - 0.64, p < 0.01) was observed between the total number of lunges performed in a match (160-240 times) and the magnitude of decrease in MVC torque (6.4-14.7%). Muscle soreness developed more (p < 0.05) for the dominant (51.5 ± 11.6 mm) than the non-dominant leg (18.8 ± 8.6 mm). CONCLUSION: Muscle damage induced by singles badminton matches was minimal, but the more the lunges are performed, the greater the neuromuscular fatigue.

Running economy and effort after cycling: Effect of methodological choices.

Prior exercise can negatively affect movement economy of a subsequent task. However, the impact of cycling exercise on the energy cost of subsequent running is difficult to ascertain, possibly because of the use of different methods of calculating economy. We examined the influence of a simulated cycling bout on running physiological cost (running economy, heart rate and ventilation rates) and perceptual responses (ratings of perceived exertion and effort) by comparing two running bouts, performed before and after cycling using different running economy calculation methods. Seventeen competitive male triathletes ran at race pace before and after a simulated Olympic-distance cycling bout. Running economy was calculated as V̇O2 (mL∙kg-1∙min-1), oxygen cost (EO2, mL∙kg-1∙m-1) and aerobic energy cost (Eaer, J∙kg-1∙m-1). All measures of running economy and perceptual responses indicated significant alterations imposed by prior cycling. Despite a good level of agreement with minimal bias between calculation methods, differences (p < 0.05) were observed between Eaer and both V̇O2 and EO2. The results confirmed that prior cycling increased physiological cost and perceptual responses in a subsequent running bout. It is recommended that Eaer be calculated as a more valid measure of running economy alongside perceptual responses to assist in the identification of individual responses in running economy following cycling.

The Agreement Between a Portable Contact-Mat and Force-Plates During Bilateral Vertical Jumps.

Force plates are commonly used when assessing vertical jumping performance but are not always affordable or practical tools for all testing situations. Twenty-four participants volunteered to take part in a study investigating the agreement between bilateral force plates and a new commercially available contact mat that records jump height, flight-time (FT), and FT of individual limbs during both countermovement (CMJ) and squat (SJ) jumps. Each participant performed six jumps of each type while standing on a contact mat placed upon a pair of in-ground force plates. When compared to the force plate via ordinary least products regression, the contact mat agreed with force plate CMJ and SJ jump height, individual limb FT during CMJs, and left-leg FT during SJs. The bilateral contact mat provided valid assessment of individual limb FT during CMJs, but not SJs. Practitioners can therefore use a bilateral contact mat interchangeably with bilateral force plates to measure SJ and CMJ performance.

Comparison of methods of derivation of the yank-time signal from the vertical ground reaction force-time signal for identification of movement-related events.

Temporal changes in ground reaction force magnitudes reflect movement strategy, and thus underlying muscle activation patterns, during movement tasks. Speculatively, these changes may be observed more readily when the force-time signal is differentiated, yielding the yank-time signal. However, the differentiation process, including the signal filtering used before or after differentiation, can significantly affect the signal-to-noise ratio (SNR) and likelihood of meaningful inference. The aim of the present study was to compare three methods of deriving the yank-time signal: Method 1 derived the yank-time signal using 2nd-order central differentiation subsequent to application of a 4th-order Butterworth filter; Method 2 included the same process as Method 1 but additionally filtered the yank-time data with a Savitzky-Golay smoothing filter; and Method 3 directly and simultaneously derived and smoothed the yank-time signal using a Savitzky-Golay digital differentiation filter. The current analyses revealed Method 2 had the best SNR, followed by Methods 3 and 1, but caused a small loss of signal amplitude. With regards to timing of inflection points in the yank-time data, no significant difference was observed. Therefore, Method 3 led to the best derivation of the yank-time signal due to its efficiency and preservation of signal characteristics and good SNR. Also, a strong association between the first maximum point of the yank-time signal and the start of the downward movement of the body's centre of mass during a countermovement jump, as identified by 3-D motion analysis, was observed. Thus, subtle events (e.g. start of downward movement) can be easily observed in the yank-time signal.