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Identification of best practices for studies of informed consent interventions would aid future systematic comparisons.
The global expansion of genetic and genomic research highlights our need to understand informed consent practices for studies in ethnically diverse cultural environments such as Africa.
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could be a valuable tool for generating standardized testing protocols, developing or improving preclinical outcome measures and cross-validating preclinical trial results using best practices for study design (described above).
The dichotomization of education into over/under 6th grade is a standard practice for studies in Guatemala [ 15].
These questions were used as a measure of disease burden which is a standard practice for studies that explore SRH [ 48].
More broadly, I justify this representation as being conceptually identical to finite element modeling (i.e. a body is tessellated into a meshwork of elements with prescribed local elasticity, Poisson ratio, etc), a well-accepted practice for studying dynamics in bodies of complex shape and/or composition.
The current best design practices for clinical studies require consideration of the assessment of end points that combine key processes and outcomes.
We have outlined the data management practices for epidemiological studies that we have modeled for our research sites in seven Asian countries and one African country.
The systematic growth of genetic and genomic research initiatives highlights the need to understand and address informed consent practices for genetic studies with diverse populations [ 2].
Based on our experience working with different groups in different research settings around the globe, we have constructed model data management practices for epidemiological studies in LDCs.
The overall sample size (35 young adults) meets best practice guidelines for studies based on semi-structured qualitative interviews [ 20].
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CEO of Professional Science Editing for Scientists @ prosciediting.com