Conducting Research with Human Participants : An IRB Guide for Students and Faculty

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Conducting Research with Human Participants : An IRB Guide for Students and Faculty

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  • 製本 Paperback:紙装版/ペーパーバック版/ページ数 328 p.
  • 言語 ENG
  • 商品コード 9781544348636
  • DDC分類 001.42

Full Description

Conducting Research with Human Participants: An IRB Guide for Students and Faculty by Nathan Durdella is the only guidebook students and faculty will need to navigate the IRB process and secure swift approval of research protocols. This book serves as an advisor to walk researchers through all the details of drafting, submission, and revision of materials for Institutional Review Boards so they can complete their research projects or dissertations faster. This text walks readers through the history of Institutional Review Boards, the contemporary context of ethical research, strategies to effectively draft, submit, and revise an IRB protocol, and guidance on working with an approved protocol in the field. The latest updates to the Common Rule and other regulatory frameworks, including special protections for working with vulnerable groups, are covered throughout the text. Not every research project goes according to plan, so adverse events and reporting receive special coverage. A final chapter on ethical research practices beyond IRB compliance encourages researchers to think through how to exit the field of research and ensure their research benefits the individuals, families, and communities in which they work. Take the guesswork out of the IRB process from start to finish with this handy guide. 

Contents

Part 1: Start Here: The Institutional Review Board Process on Your Campus
Chapter 1. Understanding Why You Submit an IRB Protocol for Review of Your Research Plans
Chapter 2. IRB Considerations Hidden in Your Research Study and Coursework
Chapter 3. Getting to Know Your Institutional Review Board
Part 2: Strategies for Success in Your IRB Protocol
Chapter 4. Categories of Review: Classification of Your Protocol
Chapter 5. The Protocol Approval Process: From Draft IRB to Final Approval
Chapter 6. Special Protections for Vulnerable Groups
Part 3: Approved Protocols: Your Roles and Responsibilities in the Research Process
Chapter 7. You're Approved to Conduct Your Study, Now What?
Chapter 8. What Happens If Something Happens: Adverse Events and Unanticipated Problems
Chapter 9. Beyond Compliance in Research Governance: Ensuring Your Work with Human Research Participants Benefits Individuals, Families, and Communities
Appendix
References

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