The on:off ratio was as follows: 6-sec tetanic stimulation followed by a rest of 20 sec, during which the participants were stimulated at 3 Hz. Data are presented as mean values ± standard error (SE). The data (EMG of SOL, GM, and GL as well as force of MVC) of each test condition (pretest, posttest, recovery) were checked for normal distribution with Kolmogorov–Smirnov test. Inhibitors,research,lifescience,medical An analysis of variance (ANOVA) for repeated measures was used to compare dependent variables. The Bonferroni correction was used to analyze differences among pairs of means. To prove the effectiveness
of the treatment, the effect sizes (f) for ANOVA (for repeated measures) were determined as follows: σ represents the standard deviation in the Inhibitors,research,lifescience,medical population and σμ is the standard deviation of the effect (Faul et al. 2007). Furthermore, to determine whether a statistically significant difference is a difference of practical concern, the selleck chem inhibitor limits of Cohen (1988) were used: f-values <0.2 indicate small, f-values <0.5 medium, and f-values <0.8 large effects (Cohen 1988). The significance level was set at P < 0.05. The Pearson coefficient of correlation
was used to examine the relationships between the muscle activities during pretest, posttest, and recovery, respectively. All www.selleckchem.com/products/Vorinostat-saha.html analyses were performed using Statistical Package for Social Sciences (SPSS, 19.0). Results The force and EMG activity of the muscles are presented Inhibitors,research,lifescience,medical in Figure 2. The data in Figure 2 are shown as percentage alteration Inhibitors,research,lifescience,medical normalized to the pretest values. EMG activity of the GL significantly decreased during NMES. In the posttest, EMG amplitude decreased from 0.501 ± 0.066 mV to 0.430 ± 0.066 mV (P < 0.01, f = 0.77, Fig. 2A). During
recovery, EMG activity increased to 0.498 ± 0.072 mV (Fig. 2A). Figure 2 Mean and standard error of the normalized electromyography (EMG) amplitudes of Inhibitors,research,lifescience,medical the (A) m. gastrocnemius lateralis, (B) m. gastrocnemius medialis, (C) m. soleus, and (D) force in the pretest, posttest, and recovery phase. The data are normalized to the … Simultaneously, EMG activity of the SOL increased during NMES from 0.507 ± 0.074 mV to 0.561 ± 0.082 mV. Difference between pretest and posttest turned out to be significant (P < 0.01, f = 1.18) (Fig. AV-951 2C). Furthermore, during recovery, the EMG amplitude still increased up to 0.577 ± 0.085 mV. EMG activity during this phase was significantly higher than during pretest (P < 0.01, f = 1.18). The results of the GM showed no significant changes between pretest and posttest (Fig. 2B). The EMG amplitude was 0.547 ± 0.076 mV and increased slightly to 0.559 ± 0.076 mV. The difference was not significant. During recovery, the EMG amplitude increased to 0.595 ± 0.084 mV. MVC did not change significantly in posttest as compared to pretest (1062.9 ± 72.4 N vs. 1097.3 ± 76.9 N, respectively). During recovery, force values increased to 1111.9 ± 66.0 N (Fig. 2D).