We provide tests of equality of mean and median values using parametric t-tests and non-parametric Wilcoxon tests
Medians and Intervals of scores obtained by physicians prior to and after the intervention Group A (Intervention) Indicator or domain Prior After [rho] * Risk factors 16 (14-32) 29 (21-26) <0,05 Clinical data 26 (17-42) 35 (23-41) <0,05 Diagnosis 14 (25-21) 22 (13-26) <0,05 Treatment 11 (7-18) 15 (12-21) <0,05 Overall competence 47 (24-74) 72 (37-96) <0,05 Group "B" (Control) Indicator or domain Prior After [rho] * Risk factors 17 (9-23) 19 (24-32) >0,05 Clinical data 23 (16-39) 25 (16-40) >0,05 Diagnosis 13 (13-23) 12 (14-23) >0,05 Treatment 12 (7-17) 14 (7-16) >0,05 Overall competence 42 (19-72) 47 (28-59) >0,05 * According to Wilcoxon test
. Source: Own elaboration based on the data obtained in the study Table 3.
Furthermore, to investigate the effect of the amount of data over evaluation results, the two selected tests were more suitable, because the Wilcoxon test
could differentiate performance differences using a small amount of data while McNemar's test needed large sample size as shown in Figure-1.
Statistical analyses SIGN TEST and WILCOXON TEST
were performed to determine the loci number with excess Heterozygosity which was based on the theory of a locus assuming mutation-drift equilibrium from 1000 interactions and that allele status changes was under IAM and SMM.
TABLE 1: Demographic data, rating scale scores, and clinical neuro-otological findings at enrollment; means [ + or -] standard deviations or numbers/percentages; P values (Wilcoxon test
and Fisher's exact test *).
Clearly, we are in crossing hazards setting, and the logrank test and the generalized Wilcoxon test
are not necessarily sensitive to this type of alternative.
Dm [micro] [m.sup.2] 10 -.968 .333 Osteoid area O.Ar [micro] [m.sup.2] 10 -.561 .575 Mineralized area Md.Ar [micro] [m.sup.2] 10 -.866 .386 Osteoblast area Ob.Ar [micro] [m.sup.2] 10 -.764 .445 P values were calculated by Wilcoxon tests
. m=number of specimens.
Antisaccade latencies and percent of errors were analyzed by non-parametric Mann-Whitney and Wilcoxon tests
Faecal cortisol levels of gorillas significantly increased in enrichment phase from 17 ng/mg in control or initial phase to 31 ng/mg (Wilcoxon tests
, n =48, z= -2.093, P < 0.05) (FIG.
The results of the Wilcoxon tests
of Risk (C.V.) during the Quiet Period versus Lock-out Period and the Wilcoxon tests
of Risk during Lock-out Period versus Post Lock-out Period are shown in Table 3.
for mean external oblique and mean peak external oblique activity between the BS and MUS were statistically non-significant (p = 0.131 and 0.286 respectively).
Because dependent variables were not normally distributed, we conducted Wilcoxon tests
to compare the number of negative and positive descriptions in the original telling phase with those in the retelling phase (see Table 1).