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  1. Legal dissemination protections in community-based participatory health equity research.Doris M. Boutain, Marie-Anne Sanon Rosemberg, Eunjung Kim & Robin A. Evans-Agnew - forthcoming - Nursing Ethics.
    Background There are legal protections for nurse researchers at public universities who employ community-based participatory research (CBPR) in research about social or health inequities. Dissemination of CBPR research data by researchers or participants may divulge unjust laws and create an imperative for university involvement. Research Question What are United States-based legal dissemination protections for CBPR health equity nurse researchers? Research Design Three case examples employing CBPR are examined: 1) a mixed methods study with participants reporting illegal discrimination in a municipal (...)
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  • Mental health, big data and research ethics: Parity of esteem in mental health research from a UK perspective.Julie Morton & Michelle O’Reilly - 2019 - Clinical Ethics 14 (4):165-172.
    Central to ethical debates in contemporary mental health research are the rhetoric of parity of esteem, challenges underpinned by the social construct of vulnerability and the tendency to homogenis...
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  • The importance of moral sensitivity when including persons with dementia in qualitative research.Anne Kari T. Heggestad, Per Nortvedt & Åshild Slettebø - 2013 - Nursing Ethics 20 (1):0969733012455564.
    The aim of this article is to show the importance of moral sensitivity when including persons with dementia in research. The article presents and discusses ethical challenges encountered when a total of 15 persons with dementia from two nursing homes and seven proxies were included in a qualitative study. The examples show that the ethical challenges may be unpredictable. As researchers, you participate with the informants in their daily life and in the interviews, and it is not possible to plan (...)
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  • Interrogating the concept of vulnerability in social research ethics.Anna Traianou & Martyn Hammersley - 2024 - Diametros 21 (80):7-22.
    This paper examines the concept of vulnerability in the context of social research ethics. An ambiguity is noted in use of this term: it may refer to an incapacity to provide informed consent to participate in a research project, or it may imply heightened susceptibility to the risk of harm. It is pointed out that vulnerability is a matter of degree, and that there are different sources and types of harm, which must be taken into account in any judgment about (...)
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  • Research ethics, informed consent and the disempowerment of First Nation peoples.Juan M. Tauri - 2017 - Research Ethics 14 (3):1-14.
    Recently, Indigenous commentators have begun to analyse the way in which institutional Research Ethics Boards engage with Indigenous researchers and participants, respond to Indigenous peoples’ concerns with academic research activities, and scrutinise the ethics proposals of Indigenous scholars. Of particular concern for Indigenous commentators is that the work of REBs often results in the marginalisation of Indigenous approaches to knowledge construction and dissemination, especially in relation to the vexed issue of informed consent. Based on analysis of the results of research (...)
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  • (1 other version)Governing Well in Community-Based Research: Lessons from Canada’s HIV Research Sector on Ethics, Publics and the Care of the Self.Adrian Guta, Stuart J. Murray, Carol Strike, Sarah Flicker, Ross Upshur & Ted Myers - 2017 - Public Health Ethics 10 (3).
    In this paper, we extend Michel Foucault’s final works on the ‘care of the self’ to an empirical examination of research practice in community-based research (CBR). We use Foucault’s ‘morality of behaviors’ to analyze interview data from a national sample of Canadian CBR practitioners working with communities affected by HIV. Despite claims in the literature that ethics review is overly burdensome for non-traditional forms of research, our findings suggest that many researchers using CBR have an ambivalent but ultimately productive relationship (...)
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  • Researching sensitive and emotive topics: The participants’ voice.Jacqueline L. Crowther & Mari Lloyd-Williams - 2012 - Research Ethics 8 (4):200-211.
    There are different groups in society who may be considered vulnerable, for example those experiencing mental or physical health issues, learning disabilities, prisoners or children. There are, however, other groups in society who may also be regarded as vulnerable, such as those who are bereaved. Vulnerability in relation to the bereaved occurs as a result of experiencing a normal life event, death or a loss. In this situation vulnerability may be transient and, depending upon the management of the bereavement, generally (...)
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  • Reporting of ethical considerations in clinical trials in Chinese nursing journals.Yanni Wu, Michelle Howarth, Chunlan Zhou, Xue Ji, Jiexia Ou & Xiaojin Li - 2019 - Nursing Ethics 26 (4):973-983.
    Background: It is acknowledged that publishers now require all primary research papers to demonstrate that they have obtained ethical approval for their research. Objectives: To assess the rate of reporting of ethical approval in clinical trials in core nursing journals in mainland China. Research design: A retrospective observational study. Participants: All clinical trials published in all of the 12 core nursing periodicals from 2016 edition China Science and Technology Journal Citation Report (core version) between 2013 and 2016 were retrieved by (...)
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  • Catholic Social Teaching as a Framework for Research Ethics.Alan J. Kearns - 2014 - Journal of Academic Ethics 12 (2):145-159.
    The importance of having ethical oversight in research that is carried out on humans is well established. Research ethics, which is mainly influenced by a biomedical ethical framework, aims to ensure that the well-being and the rights of research participants are upheld and that any potential risks and harms are reduced. However, research is also considered to be a social activity with social effects. Therefore the principles of Catholic Social Teaching as a framework for research ethics may be significant. This (...)
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  • “Money Helps”: People who inject drugs and their perceptions of financial compensation and its ethical implications.Roberto Abadie, Brandon Brown & Celia B. Fisher - 2019 - Ethics and Behavior 29 (8):607-620.
    This study documents how people who inject drugs in rural Puerto Rico perceive payments for participating in HIV epidemiological studies. In-depth interviews were conducted among a subset of active PWID older than 18 years of age who had been previously enrolled in a much larger study. Findings suggest that financial compensation was the main motivation for initially enrolling in the parent study. Then, as trust in the researchers developed, participants came to perceive compensation as part of a reciprocal exchange in (...)
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  • Ethics review, reflective equilibrium and reflexivity.Julie Morton - 2022 - Nursing Ethics 29 (1):49-62.
    Background: Research Ethics Committees (RECs) or their equivalent review applications for prospective research with human participants. Reviewers use universally agreed principles i to make decisions about whether prospective health and social care research is ethical. Close attention to understanding how reviewers go about their decision-making work and consider principles in practice is limited. Objective: The study aimed to understand how reviewers made decisions in the contexts of meetings and to understand more about how reviewers approach their work. The purpose of (...)
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  • (1 other version)Governing Well in Community-Based Research: Lessons from Canada’s HIV Research Sector on Ethics, Publics and the Care of the Self.Adrian Guta, Stuart J. Murray, Carol Strike, Sarah Flicker, Ross Upshur & Ted Myers - 2016 - Public Health Ethics 10 (3):315-328.
    In this paper, we extend Michel Foucault’s final works on the ‘care of the self’ to an empirical examination of research practice in community-based research (CBR). We use Foucault’s ‘morality of behaviors’ to analyze interview data from a national sample of Canadian CBR practitioners working with communities affected by HIV. Despite claims in the literature that ethics review is overly burdensome for non-traditional forms of research, our findings suggest that many researchers using CBR have an ambivalent but ultimately productive relationship (...)
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