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In contrast, in the current study, cognitive control as reflected by the post-conflict lateral prefrontal activation during stop success trials could only be assumed, because stop success trials by definition did not involve a reaction time.
For pS-SS trials, the first stop included both error and success trials as there were not enough of either to consider separating the two in GLM analyses.
Thus, the current work built on an assumption of greater post-conflict control in the post-stop stop success as compared to post-go stop success trials.
Using the SST, we compared stop (incongruent) with go (congruent) trials to examine conflict processing and compared stop success trials preceded by stop and go trials to examine post-conflict control, emulating previous studies of the Stroop task.
Various interventions (e.g. intradiscal electrotherapy) are also used, but despite anecdotal statements of success trials thus far have found their use to be of little direct benefit [ 119].
We recorded the Go success rate, Stop success rate, reaction time (RT) of Go success trials, the stop signal reaction time (SSRT), as well as the effect size of post-error slowing (i.e., how much participants slowed down in a Go trial following a Stop error), as an index of performance monitoring.
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A success trial was defined as any trial that resulted in the successful precision grip and removal of the food from the pin without dropping it.
Note that, unlike our previous work examining post-error slowing [12], which was a quantifiable behavioral change, a stop success trial did not involve a reaction time.
Preliminary results of the SUCCESS trial were presented by Wolfgang Janni (Heinrich-Heine-Universität, Düsseldorf, Germany).
The aim of the SUCCESS trial [ 95] is to evaluate the clinical value of CTCs in an adjuvant setting [ 96].
The SUCCESS trial partially fulfilled our dosage objective, but one half of the celecoxib patients received double the 200-mg daily dose recommended for OA patients.
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