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The first column of each subject indicates the absolute time of each trial onset referenced to the beginning of the experiment.
Trial onset was determined solely by the subjects' self-paced responses and trials occurred, on average, less than 2 s apart.
During the final 1/3 of each testing session, the 0.5 and 1.0 mg/kg exposed females took longer to enter the testing alcove at trial onset, and failed to enter the alcove more frequently than control females.
Baseline trials were time-locked and normalized to trial onset.
Before individual averaging, baselines were corrected with mean z-scores of 5 s before trial onset.
This was done to prevent observers to only rely on visual information near trial onset.
Percent signal change was calculated using the volume acquired at trial onset as baseline.
Tones, if presented, occurred 200 ms after trial onset; letters occurred randomly at 400 or 1000 ms from trial onset, giving tone-letter SOAs of 200 and 800 ms on dual task trials.
The onset of motion coherence began either 0 s, 4.5 s, or 9 s after trial onset.
The sole purpose of the latter trials was to encourage subjects to monitor for motion coherence soon after trial onset.
One second before trial onset, a warning signal (i.e., flashing yellow cross and mixed 700-Hz tone) appeared for 500 ms followed by a 500 ms delay.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com