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001481429 001__ 1481429
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001481429 019__ $$a1401648312$$a1401906336$$a1402031543
001481429 020__ $$a9783031403798$$q(electronic bk.)
001481429 020__ $$a3031403797$$q(electronic bk.)
001481429 020__ $$z9783031403781
001481429 020__ $$z3031403789
001481429 0247_ $$a10.1007/978-3-031-40379-8$$2doi
001481429 035__ $$aSP(OCoLC)1403563219
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001481429 049__ $$aISEA
001481429 050_4 $$aRA440.85
001481429 08204 $$a174.2/8$$223/eng/20231016
001481429 24500 $$aEthical issues in community and patient stakeholder-engaged health research /$$cEmily E. Anderson, editor.
001481429 264_1 $$aCham :$$bSpringer,$$c2023.
001481429 300__ $$a1 online resource (327 pages) :$$billustrations (black and white).
001481429 336__ $$atext$$btxt$$2rdacontent
001481429 337__ $$acomputer$$bc$$2rdamedia
001481429 338__ $$aonline resource$$bcr$$2rdacarrier
001481429 4901_ $$aPhilosophy and medicine ;$$vvolume 146
001481429 500__ $$aIncludes index.
001481429 5050_ $$aChapter 1. Introduction (Emily E. Anderson) -- Part 1. History, Codes of Ethics, Regulations -- Chapter 2. Theoretical roots of stakeholder-engaged research and reflections on CBPR and PCOR as a response to past research abuses (Meredith Minkler) -- Chapter 3. A philosophical justification for stakeholder engagement and key principles/a conceptual model for ethical stakeholder-engaged research (Emily E. Anderson) -- Chapter 4. Epistemology and stakeholder engagement/impact of diversity on ethical standards and practices (Kevin C. Elliott) -- Chapter 5. The limitations of the Belmont principles for stakeholder-engaged research (Elisa Hurley) -- Chapter 6. Canadas approach to regulating research with indigenous peoples (Kim Anderson) -- Chapter 7. The Council for International Organizations of Medical Sciences (CIOMS) Ethical Guidelines and Stakeholder Engagement (Alex John London) -- Chapter 8. History and philosophy of patient engagement in clinical research (Robert M. Califf) -- Part 2. Promoting Equitable Collaboration -- Chapter 9. Who represents the community? Diversity and inclusion (Ann-Gel Palermo) -- Chapter 10. Engagement for equity and sustainability; developing an equitable partnership; power-sharing, accountability, communication, conflict resolution, and trust (Giselle Corbie-Smith) -- Chapter 11 -- Capacity building and benefits to communities; Credit and compensation for community and patient stakeholders (Elizabeth Ripley) -- Chapter 12. Engaging communities in agenda setting: deciding what questions get asked and how (Alice Ammerman) -- Chapter 13. Conflicts of interest in research that engages stakeholders [individual and organizational] (Susannah Rose) -- Part 3. Stakeholder Voices -- Chapter 14. Crossing over or between two worlds The story of a someone whose engagement in research motivated them to get formal training in research or research ethics (Gigi McMillan) -- Chapter 15. A community IRB member/member of a community-based ethics review board (Bronx Community Research Review Board) -- Chapter 16. A stakeholder who has served as a PI (Sharon Terry) -- Chapter 17. A stakeholder who has served as a community advisory board member (Sandra Crouse Quinn) -- Chapter 18. The challenges of working in your own community -- Chapter 19. A patient advocates experience engaging in research -- Part 4. Human Research Protections and Research Ethics Review -- Chapter 20. Stakeholder engaged research and (the limits of) IRB review (Jennifer Cross) -- Chapter 21. Community-level risks and benefits (Lainie Ross) -- chapter 22. The principle of respect for community - a new principle (Nancy Shore) -- Chapter 23. Challenges in the field and in interactions with research participants; challenges to voluntary informed consent, privacy, and confidentiality; Moral distress among lay stakeholders (Maghbooba Mosavel) -- Chapter 24. The notion of community consent (Charles Weijer) -- Chapter 25. Community-based research review processes (Hal Strelnick) -- Chapter 26. Data ownership and deciding what gets published (Melody Goodman) -- Part 5. Case Studies: Ethics of Stakeholder-Engaged Research Across Settings -- Chapter 27. Research in emergency settings: public notification and consultation (Ryan Spellecy) -- Chapter 28. Engaging stakeholders in genomics research and the governance of biobanks (Michelle McGowan) -- Chapter 29. Engaging online patient communities in research (Elizabeth Buchanan) -- Chapter 30. Engaging patient advocates in research (Deborah Collyar) -- Chapter 31. Engaging rare disease communities (Laura P. Forsythe) -- Chapter 32. Engaging stakeholders in basic science research (Rhonda Kost) -- Chapter 33. Engaging indigenous communities/ American Indian communities in Research (Bonnie Duran) -- Chapter 34. North Americans engaging internationally (Amy Corneli) -- Chapter 35. Engaging stakeholders in environmental health research (Doug Brugge) -- Chapter 36. Engaging stakeholders in research on stigmatized health conditions (e.g., mental health, addiction, HIV) (Dennis Watson) -- Chapter 37. Engaging youth in research (Celia Fisher).
001481429 506__ $$aAccess limited to authorized users.
001481429 520__ $$aThis book provides in-depth analyses of a wide range of topics surrounding ethical issues in community and patient stakeholderengaged health research, and highlights where consensus exists, is emerging, or remains elusive. Topics in this book cover the history of stakeholder engagement in health research; how codes of ethics and regulations have (or have not) addressed stakeholder engagement; how to promote equitable collaboration; the ethical perspectives of different stakeholders; and the unique challenges posed by stakeholder- engaged research to the protection of human research participants and the research ethics review process. The book includes discussion of unique issues that arise in stakeholder engagement relevant to different populations, settings, and research designs. This book is relevant for anyone with a role or interest in stakeholder-engaged research, including patient and community research partners; academic researchers; research ethics scholars and educators; and funders.
001481429 588__ $$aDescription based on print version record.
001481429 650_0 $$aPublic health$$xResearch$$xMoral and ethical aspects.
001481429 650_0 $$aMedicine$$xResearch$$xMoral and ethical aspects.$$0(DLC)sh 85000963
001481429 655_0 $$aElectronic books.
001481429 7001_ $$aAnderson, Emily E.,$$eeditor.$$c(Editor at Eaglemoss Publications Ltd.)$$0(OCoLC)oca13731489
001481429 77608 $$iPrint version:$$tEthical issues in community and patient stakeholder-engaged health research.$$dCham : Springer, 2023$$z9783031403781$$w(OCoLC)1400793244
001481429 830_0 $$aPhilosophy and medicine ;$$vv. 146.
001481429 852__ $$bebk
001481429 85640 $$3Springer Nature$$uhttps://univsouthin.idm.oclc.org/login?url=https://link.springer.com/10.1007/978-3-031-40379-8$$zOnline Access$$91397441.1
001481429 909CO $$ooai:library.usi.edu:1481429$$pGLOBAL_SET
001481429 980__ $$aBIB
001481429 980__ $$aEBOOK
001481429 982__ $$aEbook
001481429 983__ $$aOnline
001481429 994__ $$a92$$bISE