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Using a random crossover design, 6 healthy men were exposed to cold for 120 minutes with ingestion of beverages containing low (Control, 0.04 g/min) or high (High, 0.8 g/min) amounts of glucose during the course of the experiment (study 1).
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In this study, 6 normal New Zealand white rabbits were used in a random crossover design (4 × 4 Latin square) with a 1-week washout period between trials.
The order of the testing, for both the work rate and the environment, was randomised using a random number generator in a controlled crossover design.
Recombination positions and thus breaks in ancestry on each chromosome were generated using a random walk from base pair position zero to the end of the chromosome, with ancestry crossovers occurring as a Poisson process.
We used a randomized crossover design.
An oral sugar test was performed using Karo corn syrup (karo) or stevioside in a random crossover design.
Eleven men (23.6 ± 0.7 years) were assigned to 1 of 3 trials in a random, crossover design.
For scenarios with a random crossover (figure 1B), the AT approach had nominal or close to nominal type I errors for all crossover percentages.
However, it is difficult to prove that crossover is random, and therefore assuming a random crossover may not be appropriate leading to concerns about the validity of the inference test.
We used a random-effects model.
In this study, 30 human volunteers, with no history of systemic prescription corticosteroid therapy, were given (in random order using a crossover design) two 3-day exposures of prednisone (60 mg/day) and one of identical placebo, with 11-day washouts between each medication exposure.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com