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Given that there was no significant difference between conditions in change in cognitive targets from baseline to posttreatment, as assessed by either SST negativity or PIT positive vividness, we collapsed scores across both conditions to investigate the relationship between cognitive targets and symptoms of depression.
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There was no significant difference between the two conditions in change in BDI-II from baseline to posttreatment, t(113) = 1.02, p =.31, d = 0.19, 95% CI = [ 0.17, 0.56].
There was no significant difference between the two conditions in change in BDI-II scores from baseline to posttreatment (our primary outcome), t(141.11) = 0.21, p =.83, d = 0.04, 95% CI = [ 0.29, 0.36] (see Fig. 2).
Despite having an additional area of interest on the display in the case of the CHEX condition which could have increased the chance that participants were looking in the wrong place at the wrong time fixations on the tool were minimal and there appeared to be no difference between conditions in terms of changes missed because attention was directed elsewhere.
Subjects altered their ankle kinematics between conditions resulting in changes in artificial muscle length.
To increase the chance of observing changes in histone acetylation that correlate with changes in Gcn5 localisation we used non-parametric ANOVA to identify the sets of gene ORFs that were most significantly (p<0.05) changed between conditions in Gcn5, H3K18ac or H4K16ac over all the conditions sampled.
Between-condition comparisons in the changes in EMG activity are presented in Figure 2.
Pairwise comparisons of the between-condition changes are reported in Figure 2B.
After the 2nd set, the between-condition difference in the changes from baseline was unclear for CMJ and very likely similar for DJ.
High endogenous variation within a condition can obscure between-condition changes.
To compare differences in U2AF65 binding between conditions, we corrected for changes in transcript levels by normalizing the numbers of crosslink events.
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