Responsibilities as a Researcher MCQs
Responsibilities as a Researcher MCQs
The following Responsibilities as a Researcher MCQs have been compiled by our experts through research, in order to test your knowledge of the subject of Responsibilities as a Researcher. We encourage you to answer these multiple-choice questions to assess your proficiency.
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1: Participants in a study who have been briefed by the researcher to behave in a particular way are called ____.
A. Confederates
B. Union
C. Federalist
D. None of above
2: Unobtrusive Measures are observations of people's behavior ____ them being aware of such observation.
A. With
B. Without
C. Except
D. Unless
3: The assurance given to research participants that the researcher will not release any information that will identify them is known as _____.
A. Confidentiality
B. Anonymity
C. Privilege
D. None of these
4: Anonymity is a way of protecting research participants in that the data collected from them does not identify them in any way.
A. True
B. False
5: When data cannot be used without the owner's permission, this is called _____.
A. Proprietary
B. Confidential
C. Patented
D. Public company
6: Categorical imperative is proposed by _____, a behavior is valid if one is willing to see it applied as a universal rule.
A. Immanuel Kant
B. David hume
C. Aristotle
D. Karl amx
7: The principle of the greatest good for the greatest number is called principle of _____.
A. Utilitarianism
B. Deontology
C. Hedonism
D. Altruism
8: Veil of ignorance is proposed by _____ which states that we take a dispassionate approach, reviewing all sides of a decision equally. We are asked to “wear a veil” that blinds us to all information about ourselves that might cloud our judgment.
A. John Rawls
B. Roberk nozick
C. John locke
D. None of them
9: Individuals who participate in an experiment are called _____.
A. Subjects
B. Objects
C. Topics
D. Courses
10: An international code emphasizing that research subjects must consent to the research in which they are involved and that the benefits of the research must outweigh the risks which is _____.
A. Nuremberg Code
B. Belmont report
C. Declaration of helsinki
D. Informed consent
11: The World Medical Association’s international ethical guidelines for medical professionals researching human subjects is called _____.
A. Declaration of Helsinki
B. Belmont report
C. Informed report
D. Nuremberg code
12: Informed consent is a process by which potential research participants are informed of the nature of the research and given the opportunity to sign or not sign a voluntary agreement to participate.
A. True
B. False
13: _____ outlines three basic ethical principles—autonomy, beneficence, and justice—covering research with human subjects.
A. Belmont report
B. Nuremberg code
C. Declaration of helsinki
D. Veil of ignorance
14: Autonomy is a belmont report principle
A. True
B. False
15: A Belmont Report principle that human subjects research should maximize possible benefits and minimize possible harm to participants is called _____.
A. Beneficence
B. Justice
C. Autonomy
D. Common rule
16: Justice is a ______ principle that the benefits and risks of research should be distributed fairly.
A. Belmont report
B. Declaration of helsinki
C. Informed consent
D. Nuremberg code
17: Common rule is a rule in Federal Policy for the Protection of Human Subjects.
A. True
B. False
18: Institutional Review Boards (IRBs) is a panel established to review_____ for their impact on human participants.
A. Research papers
B. Research proposals
C. Thesis
D. Patent
19: Peer review is a process of having one’s research ______ by other researchers in the author’s field prior to publication.
A. Reviewed
B. Revised
C. Edited
D. Evaluated
20: _____ is the process of ensuring that research participants receive a follow-up explanation of the research when it is completed.
A. Debriefing
B. Briefing
C. Refusing
D. Counselling
21: Search engine is a device such as Google or Yahoo that retrieves information from the ____.
A. Web
B. Internet
C. App
D. Mobile development
22: Judeo-Christian Ethic, In the context of human subjects research, the precept of not doing to others what you would not want done to yourself. This ethic is shared by many religions.
A. True
B. False
23: The 1948 Nuremberg Code emphasized that research subjects must consent to the research in which they are involved and that the benefits of the research must outweigh the risks.
A. True
B. False
24: In communication research, the term “confidentiality” means that information a participant provides ______.
A. Can be linked to the participant
B. Can be published using the participant’s real name
C. Must be published using a false name for the participant
D. Cannot be published
25: Anonymity means that the data you collect from people cannot identify them.
A. True
B. False
26: It is never possible to use e-consents for your research.
A. True
B. False
27: Professional codes of conduct generally allow deception in research designs as long as the participants are made aware of the deception immediately after the study is concluded.
A. True
B. False
28: Proprietary information is information that may be reproduced without permission.
A. True
B. False
29: Unobtrusive measures research is based on the assumption that people’s permission must be obtained before observing their behavior.
A. True
B. False
30: What is the “Common Rule”?
A. Standardized way of measuring communication activity
B. Federal policy for the protection of human subjects in research
C. Research protocol used in the European Community
D. Federal requirement that requires all federally funded research to be completed within a defined time
31: In communication research, the term “anonymity” means that information a participant provides ______.
A. Can be published using the participant’s real name
B. Must be published using a false name for the participant
C. Cannot be published
D. Cannot be linked to the participant
32: Researchers have an ethical responsibility to readers of their research reports as well as to their research participants.
A. True
B. False
33: In communication research, a “confederate” is a research participant who ______.
A. Has signed a consent form
B. Has been selected because of his or her political orientation
C. Is not being paid to participate
D. Has been briefed by the researcher to behave in a particular way
34: The overall focus of codes of ethics in human communication research is to protect the researcher from legal action.
A. True
B. False
35: A literature review is your summary and evaluation of what other researchers working on your topic have published.
A. True
B. False
36: An IRB is a panel established to review research proposals for their cost-effectiveness.
A. True
B. False
37: Researchers should promptly respond to participants’ requests for information about the nature, results, and conclusions of the research they are participating in.
A. True
B. False
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Responsibilities as a Researcher MCQs
