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This selection process produced a reasonable feasibility sample of 30 patients who generously participated in the interview.
For a feasibility test, sample databases of tool catalogs and the machining instance data of heat resistant super alloys are implemented and used.
For a feasibility study, sample size is not established based on power to detect an anticipated intervention impact.
As this was a proof-of-concept study primarily aimed at assessing feasibility, sample size calculations were not performed.
The feasibility sample size was 20 patients.
Such a national incidence cohort does not exist for obvious reasons, including cost, feasibility, sampling biases and ethical considerations.
However, the feasibility (samples size, resources, ethics) and the clinical relevance of the results should be evaluated before designing any new study.
As this was a feasibility trial, no sample size power calculations were undertaken.
As this was a feasibility study, our sample size was based on pragmatic considerations: the number of patients consulting at the chest pain clinic over the course of the data collection phase of the study.
As this is a feasibility study, the sample size is not based on a statistical power calculation; rather the purpose of the study is to test feasibility in three different primary care settings, and so sample size is tailored to logistical limitations inherent in the different trial settings.
As this is a feasibility study, a formal sample size calculation was not undertaken.
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CEO of Professional Science Editing for Scientists @ prosciediting.com