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In each trial, a sample is drawn from the maximum entropy distribution and its G value is compared to the G value of the empirical distribution.
To address the aims of a pilot trial a sample size justification is required.
On each trial, a sample stimulus was presented on the left side of a computer screen and two comparison stimuli presented on the right.
Since this was a phase I/II clinical trial, a sample size of 30 50 was considered prudent for this study.
At the start of this trial, a sample size of 250 persons was selected to provide 80% power to detect a reduction in the incidence of a defined set of acute complications from 30%to15%5% at p=0.05.
In this trial, a sample of families of 5th 7th grade students from three school districts were randomly assigned to MSFP, the original SFP program, or a wait-list control group and completed pre- and post-intervention self-report assessments.
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13 For trial A, samples were first soaked in the simulated saliva for 15 s (37 °C).
For trial A, samples were first soaked in the simulated saliva for 15 s (37°C).
Sensitivity analyses were robust (see Additional file 6) by excluding unpublished trials, trials with a sample size less than 40 and trials with unclear randomization procedure.
For single-arm trials, a sample size of 30 was used; for two-arm trials, 150 (75 per arm) was used.
Each trial comprised a sample run and a choice run.
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CEO of Professional Science Editing for Scientists @ prosciediting.com