Dewey Decimal174/.915
Table Of ContentPart 1: Start Here: The Institutional Review Board Process on Your CampusChapter 1. Understanding Why You Submit an IRB Protocol for Review of Your Research PlansChapter 2. IRB Considerations Hidden in Your Research Study and CourseworkChapter 3. Getting to Know Your Institutional Review BoardPart 2: Strategies for Success in Your IRB ProtocolChapter 4. Categories of Review: Classification of Your ProtocolChapter 5. The Protocol Approval Process: From Draft IRB to Final ApprovalChapter 6. Special Protections for Vulnerable GroupsPart 3: Approved Protocols: Your Roles and Responsibilities in the Research ProcessChapter 7. You're Approved to Conduct Your Study, Now What?Chapter 8. What Happens If Something Happens: Adverse Events and Unanticipated ProblemsChapter 9. Beyond Compliance in Research Governance: Ensuring Your Work with Human Research Participants Benefits Individuals, Families, and CommunitiesAppendixReferences
SynopsisFounded in 1965, SAGE is a leading independent academic and professional publisher of innovative, high-quality content. Known for our commitment to quality and innovation, SAGE has helped inform and educate a global community of scholars, practitioners, researchers, and students across a broad range of subject areas. Book jacket., 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., Conducting Research with Human Participants is the only guidebook readers will need to navigate the IRB process and secure swift approval of research protocols. This text walks readers through the history of IRBs, strategies for drafting and revising protocols, and guidance on working with an approved protocol in the field.
LC Classification NumberBF181