Question

Who is Stanley Milgram and what happened in his famously discussed experiment?

Describe the methods used to carry out the study. (Hint: what was the role of the learner?

What was the role of the teacher? What was the role of the experimenter?)

What was Milgram trying to investigate?

How are his findings applicable in the real world?

What is the Belmont Report and why was it developed?

Why is informed consent necessary to get? Who does it protect? What does it include?

What is the importance of debriefing?

Know general details of the Tuskegee study and be able to discuss why the methods used in that study were unethical.

What does the acronym IRB stand for?

-What is the function of an IRB? What kind of research do they help regulate? Where do they regulate research? Why do they include researchers and Laypeople (non-scientists) on

their committees?

-Understand the 3 different levels of risk in studies. What are they? List them.

-What are the 5 principles of the APA Ethics Code: A) Beneficence B) Fidelity and Responsibility C) Integrity D) Justice E) Respect for Peoples Rights and Dignity

-How do we assess risk and benefit in research?

-What are some variables that may contribute to risk in research?

Answer 1

Question-1

Stantly milligrams was a psychologist in Yale univesity He conducted an expriment , focusing on conflict obedience to authority and personal conscience.

The role of learner was taken into room and had elctrodes attached to his armed.and the teacher and experimenter went next room door where contained elctrec shock and raw of switches mark 15 voltes to 375 voltes.

Miligram trying to investigate how ordinary people could be influencing in commiting atrocities for example German in WWII.

Informed concent necessary to get participation active involvement where participation come to know details on the study , so that they can inform , voluntary and rational decision to participate and understand the purpose of study.

The acronym of IRB is institutional review board , a medical oversight committee that govern or investigate human subject .The purpose of the to protects of the right and health of participants in clinical trials.