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Umfang: 1 online resource (262 p.)

ISBN: 9781786390066 , 178639006X , 9781786390059 , 1786390051

Inhalt: This book is a collection of fictionalised case studies of everyday ethical dilemmas and challenges, encountered in the process of conducting global health research in places where the effects of global, political and economic inequality are particularly evident. It is a training tool to fill the gap between research ethics guidelines, and their implementation 'on the ground'. The case studies, therefore, focus on 'relational' ethics: ethical actions and ideas that emerge through relations with others, rather than in regulations.

Anmerkung: Description based upon print version of record. , English

Weitere Ausg.: ISBN 9781786390042

Weitere Ausg.: ISBN 1786390043

Sprache: Englisch

UID:

Umfang: 1 online resource (340 pages)

Ausgabe: 1st ed.

ISBN: 9781786390066

Anmerkung: Intro -- Cover Page -- Title Page -- Copyright Page -- Forewords -- Preface -- Acknowledgements -- Contents -- Finding your way around the book -- INTRODUCTION -- PART ONE: TRAINING CASE STUDIES -- Researcher-participant relationships -- 1. Fieldwork and friendship: working in your own community -- 2. Soap and persuasion: recruiting and caring for participants -- 3. Gel and/or condoms: safety in a microbicide trial -- 4. Friends like how?: getting personally involved with participants -- 5. Readability and sweet talk: the translation and comprehension of study documents -- 6. We don't pay: 'bus fares' and other gifts in research -- 7. Your friend has nice clothes: confidentiality and staff identity in HIV home follow-up -- 8. Truth and lies: doing fieldwork in your own community -- 9. I could be a sex worker: meanings of exclusion and inclusion criteria to participants -- 10. They just come and ask questions: participants' understanding of the purpose of research -- 11. Responsibility for what and whom?: end-of-trial and long-term healthcare -- 12. Hunger is not our mandate: dealing with poverty among research participants -- 13. They just want to sign quickly: different interpretations of informed consent -- 14. Martha's dilemma: foreign medical research as public good or exploitation? -- 15. Routine healthcare: whose obligation? -- Community and family relationships -- 16. Everybody's corrupt: understanding suspicion in medical research -- 17. Bad press: the origins and impact of 'blood stealing' rumours -- 18. People will always talk: protecting participants from stigma in an HIV study -- 19. Lost in translation: public communication and power relations -- 20. Husband out of town: gender relations and decision-making -- 21. Chop your money!: challenges in recruitment and enforcing study rules. , 22. My husband doesn't know: involving male partners in microbicide research -- 23. Of course we speak English: community engagement and disseminating information -- 24. Satanists or scientists?: dealing with negative associations 128 -- 25. The Sheep Study: old memories of food, blood and death -- 26. Will they leave us where we are?: expectations of medical research interventions -- 27. Seeing is believing: trial regulations vs. community engagement in an Ebola vaccine trial -- Institutional relationships -- 28. Too many people have turned up!: addressing stakeholders' concerns -- 29. Data troubles: collaboration and the future of partnership -- 30. Between envy, suspicion and desire: embedding research in government healthcare facilities -- 31. The end of a trial: post-trial responsibilities and relationships -- 32. Helping hand: working with public hospitals -- 33. Whose capacity?: collaboration through capacity building -- 34. Like a market: competitive recruitment and double enrolment -- 35. Under one roof: sharing resources in a district hospital -- 36. We will not do your work for free: incentives, per diems and professional culture -- 37. Is it a gift, really?: drug donations, access and social benefit -- Staff relationships -- 38. Per diem: practical inequalities in scientific collaboration -- 39. Do anthropologists know best?: relationships between social scientists and medical researchers -- 40. Who are you?: employment issues and North-South relationships -- 41. Snot for sale: staff's handling of transport reimbursement and rumours -- 42. I'm sure you'll give her a chance: employment and corruption -- How to use the case studies -- Guidance for facilitators -- Facilitator's preparation template -- First experiences of piloting this tool in Africa and Europe -- Resources -- PART TWO: ACADEMIC BACKGROUND. , Academic background: ethical deliberation, engaged conscience, and conscious choice -- The context of global health inequality -- Inequality and discomfort -- Emergent debates -- We need to talk more -- we need to do more -- REFERENCES -- INDEX OF CASE STUDIES -- Case studies by learning objective -- Case studies by keyword -- ABOUT THE CONTRIBUTORS -- Footnote -- Academic Background.

Weitere Ausg.: Print version: Aellah, Gemma Global Health Research in an Unequal World Oxford : CAB International,c2016 ISBN 9781786390042

Sprache: Englisch

Schlagwort(e): Electronic books. ; Electronic books

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UID:

Umfang: 1 online resource (262 pages)

ISBN: 9781786390066

Inhalt: Cover Page -- Title Page -- Copyright Page -- Forewords -- Preface -- Acknowledgements -- Contents -- Finding your way around the book -- INTRODUCTION -- PART ONE: TRAINING CASE STUDIES -- Researcher-participant relationships -- 1. Fieldwork and friendship: working in your own community -- 2. Soap and persuasion: recruiting and caring for participants -- 3. Gel and/or condoms: safety in a microbicide trial -- 4. Friends like how?: getting personally involved with participants -- 5. Readability and sweet talk: the translation and comprehension of study documents -- 6. We don't pay: 'bus fares' and other gifts in research -- 7. Your friend has nice clothes: confidentiality and staff identity in HIV home follow-up -- 8. Truth and lies: doing fieldwork in your own community -- 9. I could be a sex worker: meanings of exclusion and inclusion criteria to participants -- 10. They just come and ask questions: participants' understanding of the purpose of research -- 11. Responsibility for what and whom?: end-of-trial and long-term healthcare -- 12. Hunger is not our mandate: dealing with poverty among research participants -- 13. They just want to sign quickly: different interpretations of informed consent -- 14. Martha's dilemma: foreign medical research as public good or exploitation? -- 15. Routine healthcare: whose obligation? -- Community and family relationships -- 16. Everybody's corrupt: understanding suspicion in medical research -- 17. Bad press: the origins and impact of 'blood stealing' rumours -- 18. People will always talk: protecting participants from stigma in an HIV study -- 19. Lost in translation: public communication and power relations -- 20. Husband out of town: gender relations and decision-making -- 21. Chop your money!: challenges in recruitment and enforcing study rules.

Anmerkung: Description based on publisher supplied metadata and other sources

Weitere Ausg.: ISBN 9781786390042

Weitere Ausg.: Erscheint auch als Druck-Ausgabe ISBN 9781786390042

Sprache: Englisch

URL: lizenzpflichtig

Mehr zum Autor: Geissler, Paul W.