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In the first stage, trial analyses were conducted to enable the input data such as material properties to reproduce the monitored deformation response of tunnel.
By using single trial analyses, fixations to target and distractors could be decoded from the EEG signals above chance level in 11 out of 12 subjects.
The handling of item-level missing data is a focus of statistical consideration in clinical trial analyses; in this study, item-level missing data were treated as a random effect for each of the measures and an additional pattern analysis was conducted, to account for this effect.
The non-incentive trial data (as the control condition) was incorporated twice, once in each of the reward and loss-avoidance trial analyses.
This assumption is conventional in trial analyses.
Combined trial analyses were followed by separate analyses of the E and E + P trial data.
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Individual and trial-by-trial analyses showed asynchronies between changes in strategic behavior and recall (e.g., increased strategy production but decreased recall), which indicate a utilization deficiency.
We employed single-trial analyses of neurophysiological and behavioral data recorded during a WM paradigm, designed to include predictable distractors, on 18 patients with an at-risk mental state for psychosis (ARMS, 26.1 ± 5.45 years) and 21 healthy controls (HCs, 25.5 ± 3.95 years).
In post-trial analyses, blame for the outcome varied.
Ten within-trial analyses [ 32, 39- 47] 47] used a straightforward method to calculate the effectiveness and cost.
Additional within-trial analyses showed no differences between cohorts in randomization statuses, nor in the likelihood of having an AD-affected FDR (ARP, 63%; SRP, 69%; P = 0.293).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com