Principles and Practice of Clinical Research 2012
DOI: 10.1016/b978-0-12-382167-6.00013-8
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National Institutes of Health Policy on the Inclusion of Women and Minorities as Subjects in Clinical Research

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Cited by 7 publications
(2 citation statements)
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References 19 publications
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“…Many people had predicted that women would not want to participate in clinical research, but as many studies later documented, I found enthusiasm in communities of women for a role in research. Once women were informed about the benefits to future medical knowledge and care and about the historical examples of conclusions from research applied to women but based on studies of men, they were eager to learn how they could participate (34,35).…”
Section: Inclusionmentioning
confidence: 99%
“…Many people had predicted that women would not want to participate in clinical research, but as many studies later documented, I found enthusiasm in communities of women for a role in research. Once women were informed about the benefits to future medical knowledge and care and about the historical examples of conclusions from research applied to women but based on studies of men, they were eager to learn how they could participate (34,35).…”
Section: Inclusionmentioning
confidence: 99%
“…The underrepresentation of women in research, especially pregnant women in clinical trials for reasons of safety (woman and fetus), is a longstanding issue in research. 22,23 The exclusion of minority groups, for example African Americans in the United States, 24 on the grounds of feasibility or concerns of mistreatment, or being taken advantage of, has also been highlighted as a major concern in the research literature. Migrant populations present unique challenges, including their linguistic and cultural diversity and implications related to their migration status, for example, the precarity of their situation and lack of knowledge of their rights.…”
Section: Introductionmentioning
confidence: 99%