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Ethical Issues in Community and Patient Stakeholder-Engaged Health Research
Title
Ethical Issues in Community and Patient Stakeholder-Engaged Health Research [electronic resource] / edited by Emily E. Anderson.
ISBN
9783031403798
Edition
1st ed. 2023.
Publication
Cham : Springer International Publishing : Imprint: Springer, 2023.
Physical Description
XVI, 327 p. 1 illus.
Local Notes
Access is available to the Yale community.
Access and use
Access restricted by licensing agreement.
Summary
This book provides in-depth analyses of a wide range of topics surrounding ethical issues in community and patient stakeholder-engaged 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.
Variant and related titles
Springer ENIN.
Other formats
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Printed edition:
Printed edition:
Format
Books / Online
Language
English
Added to Catalog
October 03, 2023
Series
Philosophy and Medicine, 146
Contents
Chapter 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. Canada's 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 advocate's 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).
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