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Respondents were randomised to one of the 10 survey versions.
These 397 respondents were randomised to receive the study interventions and were mailed the post-intervention survey booklet.
Two months after the first mailing, respondents were randomised at the practice level to one of the four study groups and then mailed the second survey.
Respondents were randomised (table 2) to either no information or combinations of information on disease severity (severe v moderate) and expected benefits of treatment (high v low).
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Ten percent of respondents' data were randomised by using Microsoft Excel software.
Having responded to the complete SIAS version to which they were randomised, all respondents were then asked the other version of item 14.
Students were randomised using simple randomisation.
Only persons responding by the mode to which they were randomised, were included in these analyses; cross-over respondents were treated as non-respondents.
In this trial, 74 smokers were randomised in two groups.
Initially women were randomised to receive either trastuzamab or lapatinib or no treatment.
The sequence of target velocity and initial ramp direction were randomised.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com