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An analysis of these indicates that: this literature is in the early stages of knowledge development; interviews/focus groups dominate data collection methods; nonprobability samples are almost always used; even basic demographic data is scarce; and the relationships among and between all participants in the fostering process likely to affect the quality of the fostering experience.
Basic demographic data is shown in Table 1.
Classification of the patients according to the tests used and their basic demographic data is given in Tables 1 and 2. The 60 ST seropositive patients from cohort 1, the 33 ST seropositive patients and the 118 SFG seropositive patients from cohort 2 and the 75 ST seropositive patients and 80 SFG seropositive patients from cohort 3 were considered for the clinical profiling.
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Basic demographic data was collected about the interviewees, including where they lived, their age and ethnicity, educational qualifications, previous criminal history and whether they worked.
Basic demographic data was collected for each participant.
The basic demographic data are described in Table 1.
The basic demographic data were listed in Table 1.
Basic demographic data was collected, including questions about age, gender, marital status and specialty choice.
Basic demographic data was collected on 38,228 people (50.3% male and 49.6% females).
Basic demographic data were examined using Chi-square tests for categorical data and t-tests for continuous data.
Also basic demographic data was collected and each patient consultation was registered with date, type of treatment and profession.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com