Description: The course is organized in two parts: Part I studies the history of research regulations, requirements for ethical research, informed consent, institutional review boards, protection of special at-risk populations, deception in research, and future directions of regulations on research. Each participant presents a research design and the class analyzes its legal aspects. Part II focuses on ethical issues in clinical research.
Description: Provides an asynchronous, engaging, and interactive way to understand the U.S. healthcare system and gain insight about the system. This online course requires assigned course work and attendance a 90-minute in-person group session during weeks 4-5 of the course. Registration for group session is required early in the course.
Course Goals: This course provides students from a wide variety of academic backgrounds an asynchronous finding that medical students are far less confident about their health policy knowledge than their clinical preparation. The course developers have formulated the learning materials to be accessible and engaging for students from multiple different fields and levels of study.The course is designed to have a very favorable effort-to-learning ratio with engaging instructional material and high-yield suggested readings. Learning formats include:- didactic material (Week 1)- documentary-style archival material (Week 2)- in-depth expert interviews (Week 3)- simulation exercises (Week 4)- on-campus in-person discussion groups to engage in conversations about health plan and health system design (Week 5)- an expert panel discussion of the future of healthcare in the US (Week 6).
Competencies: 1. Understand the main players (stakeholders) in the US healthcare system 2. Be able to identify examples of synergistic versus conflicting actions of the main players in the healthcare system 3. Expand their understanding of the history of healthcare reform in the United States.