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Five questions that need answering when considering the design of clinical trials

Overview of attention for article published in Trials, July 2014
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Title
Five questions that need answering when considering the design of clinical trials
Published in
Trials, July 2014
DOI 10.1186/1745-6215-15-286
Pubmed ID
Authors

Timothy Clark, Hugh Davies, Ulrich Mansmann

Abstract

Evidence suggests that research protocols often lack important information on study design, which hinders external review. The study protocol should provide an adequate explanation for why the proposed study methodology is appropriate for the question posed, why the study design is likely to answer the research question, and why it is the best approach. It is especially important that researchers explain why the treatment difference sought is worthwhile to patients, and they should reference consultations with the public and patient groups and existing literature. Moreover, the study design should be underpinned by a systematic review of the existing evidence, which should be included in the research protocol. The Health Research Authority in collaboration with partners has published guidance entitled 'Specific questions that need answering when considering the design of clinical trials'. The guidance will help those designing research and those reviewing it to address key issues.

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Mendeley readers

The data shown below were compiled from readership statistics for 63 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 63 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 13 21%
Researcher 10 16%
Student > Ph. D. Student 9 14%
Student > Postgraduate 8 13%
Other 5 8%
Other 12 19%
Unknown 6 10%
Readers by discipline Count As %
Medicine and Dentistry 26 41%
Biochemistry, Genetics and Molecular Biology 5 8%
Agricultural and Biological Sciences 5 8%
Mathematics 4 6%
Social Sciences 3 5%
Other 10 16%
Unknown 10 16%