University of California, Irvine. (December 4, 2010, Sapporo, Japan)
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1 University of California, Irvine 1 2 (December 4, 2010, Sapporo, Japan) This article is an invaluable record of an interview with Prof. Ruth Mulnard, who is a nursing scientist as well as a clinician in United States, who has especially focused on the area of dementia and has extensive experience of working as a principal investigator (PI) of 20 to 30 protocols of clinical trials. There seems to be no other nurse who has such experience. This became possible not only because she herself has the ability to formulate research questions and design protocols, but also because there are physicians on her team to work with her taking responsibility as physicians to prescribe drugs, overseeing medical care, controlling adverse events, etc. Her experience of working a long time as a chairperson of an ethics committee is extremely important. In this regard, she presents a model for other researchers to use in order to conduct highly ethical research just as she has required of other applicant researchers, as chair of the committee. She also has experience to lead activities to revise the California law on informed consent for research participation to benefit cognitive impaired patients; to develop guidelines for gathering brain tissue and banking it at Alzheimer s centers across the country, funded by the National Institute on Aging. She also introduced her success in the debate to conclude that, in case any incidental findings not related to the research questions are found during the research, the researcher should give the patients-subjects appropriate referral and introduce them to a medical facility where they can be properly cared for. Several kinds of rare, significant experience have led her to become an outstanding characteristic role model of a contemporary nursing scientist and clinician. principal investigator (PI), nursing science, research ethics, informed consent, dementia 1
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