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However, the most common response to hearing this and other new information was: "Explain to us why and how this works and we might believe you".
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Before enrollment, the trial information was explained carefully to each patient, and subsequently written informed consent was obtained from all participants.
In addition, before the execution of the case study, the purpose of the study and the absolute confidentiality of personal information was explained to each volunteer.
The purpose for seeking information was explained in detail to individual patient.
Where possible, the information was explained in a simple format, including pictographs where necessary to communicate risks.
Participants signed the forms after all of the information was explained to them by the data collectors.
This information was explained by a prevention technician and a talk was given to each work party prior to the activity.
However, after entering these variables in the model still part of the probability of receiving information was explained by the hospital in which patients were operated.
Furthermore, logistic multilevel analyses revealed that the probability of receiving information was explained by the hospital in which patients were operated.
In case of illiterate women all research information was explained verbally in the local dialect with a thumb print accepted in lieu of a signature, following standard practice in the context.
How should missing information be explained?
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com