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Politicians are pushing school boards to do more to ensure students leave school with the financial literacy skills they will need to navigate an increasingly complex financial marketplace. Financial literacy education must start early to achieve this goal, yet there has been very little Canadian research on financial literacy education at the elementary level. This exploratory study used an anonymous, online survey to gain a preliminary understanding of full-time Ontario elementary teachers' perceptions, attitudes, and practices with respect to financial literacy education. Respondents overwhelmingly favour teaching financial literacy in elementary school. Almost half of respondents currently incorporate financial literacy into their classroom practice. These teachers rely primarily on free, online resources. With respect to barriers to teaching financial literacy, respondents cited the lack of an appropriate curriculum and lack of support from schools and school boards. Respondents identified professional development as the main type of support they would like to see schools and school boards provide to support them in teaching financial literacy going forward. Keywords: financial literacy, financial education, elementary teachers ; Les politiciens poussent les conseils scolaires à en faire davantage pour s'assurer que les étudiants finissent leurs études avec les compétences financières dont ils auront besoin pour naviguer sur un marché financier de plus en plus complexe. Bien qu'il faille commencer tôt pour atteindre cet objectif, il existe très peu de recherches canadiennes sur l'éducation financière au primaire. Cette étude exploratoire a utilisé un sondage anonyme en ligne pour obtenir une compréhension préliminaire des perceptions, attitudes et pratiques des enseignants à temps plein du primaire en Ontario quant à l'éducation financière. Les répondants sont très majoritairement favorables à l'enseignement de la littératie financière au primaire, et près de la moitié d'entre eux l'intègrent déjà dans leur ...
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In: IRB: ethics & human research, Band 23, Heft 2, S. 13
ISSN: 2326-2222
Scientists are turning to genetic variation research in hopes of addressing persistent racial/ethnic disparities in health. Despite ongoing controversy, the advancement of genetic variation research is likely to produce new knowledge and technologies that will substantially change the ways in which we understand and value health. They also may affect the ways in which individuals and groups organize socially, politically, and economically.
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In: International labor and working class history: ILWCH, Heft 61, S. 180-182
ISSN: 0147-5479
In: Administrative Science Quarterly, Band 31, Heft 1, S. 163
In: IRB: ethics & human research, Band 26, Heft 2, S. 13
ISSN: 2326-2222
In: Studies in Social Medicine Ser
Cover -- Contents -- Acknowledgments -- Introduction -- Chapter One. It Shouldn't Take a Pandemic: Social Determinants of Health and Illness -- Chapter Two. Lifeboat Ethics, Social Selves, and Health Justice -- Chapter Three. Lifeboat Frameworks, Certification, and the Work of Clinical Bioethics -- Chapter Four. How Neglecting Health Disparities Promotes a Truncated Research Agenda -- Chapter Five. Bioethics and the Global Warming Crisis -- Conclusion -- Notes -- Bibliography -- Index -- A -- B -- C -- D -- E -- F -- G -- H -- I -- J -- K -- L -- M -- N -- O -- P -- Q -- R -- S -- T -- U -- V
In: Pacific affairs: an international review of Asia and the Pacific, Band 58, Heft 2, S. 319
ISSN: 1715-3379
The regulations governing human subjects research (45 CFR 46) remain largely unchanged since their adoption. As a first step in their revision, the federal government published the Advance Notice of Proposed Rule Making (ANPRM) in 2011. The public responded with over 1100 comments. We selected a random sample of 300 comments, examining whether they addressed biospecimen research in terms of views on mandated consent, waivers of consent, use of a short general consent form, or identifiability of biospecimens. We conducted content analysis on the 109 comments that fulfilled these criteria Findings reveal little support for the proposal to mandate consent, strong support for the current waiver system, confusion about use of a standard general consent form, and disagreement about the implications of biospecimen identifiability. As the government moves ahead in its rulemaking process, it is important to consider what the public comments reveal about support and/or concerns for proposed changes.
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In: Life sciences, society and policy, Band 9, Heft 1
ISSN: 2195-7819
In: Journal of empirical research on human research ethics: JERHRE ; an international journal, Band 2, Heft 2, S. 41-48
ISSN: 1556-2654
Considerable variation has been demonstrated in applying regulations across research ethics committees (RECs) in the U.S., U.K., and European nations. With the rise of international research collaborations, RECs in developing countries apply a variety of international regulations. We conducted a qualitative descriptive pilot study with members of the national REC in Malawi to determine criteria they use to review research, and their views on international collaborations. Qualitative content analysis demonstrated that international guidelines are interpreted in light of local African conditions such that emphasis is placed on examining benefit to the community and ensuring the informed consent process translates concepts in locally-meaningful ways. Members suggest that RECs often must comply with regulations that do not fit local conditions. Recommendations are provided for improving such international collaborations.
In: Ethics & human research: E&HR : a publication of the Hastings Center, Band 41, Heft 3, S. 13-22
ISSN: 2578-2363
ABSTRACTThe relationship between risks and benefits is central to the ethics of research involving human participants. Traditionally, to be ethically justifiable, risks should be reasonable in relation to anticipated benefits (if any) to subjects and to the potential social benefits resulting from research. This calculus is being further complicated by findings from an increasing number of social science studies that reveal that prospective and actual research participants frequently describe various types of inclusion benefits (for example, personal benefits such as access to or improved health care, increased knowledge about their disease or condition, and greater solidarity with the local community) as important to them. What is the ethical significance of such inclusion benefits, particularly those nonmedical in nature, for research ethics committees' risk‐benefit assessment of research studies? We argue that, unless participants are clearly mistaken in their perceptions, ethics committees should take these types of inclusion benefits into account, and we suggest a few ways this might look in practice.