This is the third and final article of a three-part series that follows up the discussion on the fundamentals of writing research protocols for quantitative clinical research studies. In this editorial, the authors discuss key elements of data collection, data analysis, and the ethical considerations and implications that come with clinical research. This editorial is the concluding segment on providing guidelines for undergraduate researchers interested in publishing their protocol in the Undergraduate Research in Natural and Clinical Sciences and Technology (URNCST) Journal.Keywords: data collection; questionnaires; analysis; descriptive statistics; clinical ethics; informed consent; research ethics board; undergraduate research; research protocol; clinical research
IntroductionThe final segment of the three-part series focuses on data collection, data analysis, and the ethics of clinical research studies. The authors first describe data collection in clinical research and then explore how undergraduate investigators may collect valid, useful data through questionnaires and how to analyze quantitative data appropriately. The authors conclude this paper by identifying the ethical considerations in conducting clinical research.