Exam 3: Ethical Guidelines for Research
When research is reviewed concerning populations vulnerable to coercion or undue influence, such as prisoners, the IRB must include a member ______.
C
Zimbardo's Stanford Prison Experiment lasted ______.
C
What is known as the Common Rule? What does it say?
The Department of Health and Human Services (DHHS) and the Food and Drug Administration then translated these principles into specific regulations that were adopted in 1991 as the Federal Policy for the Protection of Human Subjects also known as the Common Rule (Title 45 of Code of Federal Regulations [CFR], Part 46). This policy has shaped the course of social science research ever since, by requiring organizations that sponsor federally funded research-including universities-to establish committees that review all research proposed at the institution and ensure compliance with the federal human subjects requirements when the research is conducted. This policy has shaped the course of social science research ever since. This section introduces these regulations.
After 25 years, the Common Rule was revised, with modifications that were supposed to be implemented in January of 2018 but were delayed at the last minute, and the effective date was moved to July 19, 2018 (Allen, 2018). The revisions relaxed some requirements for social science research and made several other important changes that are consequential for both medical and social science researchers. These regulations, as revised, inform the discussion that follows (Chadwick 2017).
Describe the design of Milgram obedience experiments. What were some of the controversies surrounding it?
Discuss some of the widely publicized abuses in research that made it clear that formal review procedures should be put into place to protect research participants. As part of your discussion, include the Nuremberg War Crimes trials, the Tuskegee Syphilis experiment, and Milgram's obedience experiments.
Institutions seeking federal funds for research involving human subjects must have a group that reviews research proposals.
What was the Belmont Report? What were the three ethical principles it established?
The Health Insurance Portability and Accountability Act (HIPAA) passed by Congress in 1996 had very little effect on the protection of health care data
The process and even possibility of obtaining informed consent must take into account the capacity of prospective participants to give informed consent.
Briefly describe the historical development of formal procedures for the protection of human subjects in research. Be sure to include some of the notorious human rights cases that led to the creation of the first Ethics Committees.
Milgram's (1963) obedience experiments highlighted the atrocities committed under the Nazis by ______.
Today, federal regulations require that every institution that seeks federal funding for biomedical or behavioral research on human subjects ______.
In 2017, there was a revision of the 1991 Federal Policy for the Protection of Human Subjects, which ______.
What is an IRB? What does it do? Do other countries have similar entities?
What were the ethical issues with Zimbardo's research? Did he receive valid results? Did everyone agree that he did?
Openness about research procedures and results goes hand in hand with honesty in research design.
Who determines whether deception of research participants is justifiable?
There are special protections in place regarding research involving ______ populations.
Research participants should feel no anxiety or distress whatsoever during the study or even after their involvement ends.
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