Chapter 3 Flashcards

1
Q

Set of ethical guidelines, develop for research with human participants based on information gained during the nuremberg trials after World War II

A

Nuremberg code

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2
Q

Obtaining consent from participants for participation in research after the Participants have been informed about the process, procedure and risk of the research

A

Informed consent

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3
Q

Forcing participants to participate in research without their consent

A

Coercion

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4
Q

Misleading participants about the purpose of procedures of a research study

A

Deception

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5
Q

A person who is part of a research study, but acts as though he or she is not to deceive the participants about the study purpose

A

Confederate

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6
Q

Discussing the purpose and benefits of a research study with Participants often done at the end of the study

A

Debriefing

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7
Q

A form provided to the Participants, at the beginning of a research study to obtain their consent for the study, and to explain the studies, purpose and risk and the participants right as participants

A

Consent form

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8
Q

Wayne, the risk against the benefit of a research study to ensure that the benefit outweighs the risk

A

Risk benefit analysis

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9
Q

The researchers responsibility to protect the participants identity and right to privacy during, and after the research study

A

Confidentiality

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10
Q

A committee of knowledgeable individuals who oversee the ethics of research with human participants conducted at an institution

A

Institutional review board

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11
Q

A source of bias that can occur in a study due to participants, changing their behavior based on their perception of the study, and its purpose

A

Demand characteristics

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12
Q

And experiment conducted in the participants natural environment

A

Field experiment

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13
Q

Study with the smallest amount of risk involved

A

Exempt studies

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14
Q

Cities that involve minimal risk, need to be reviewed by only one member of the IRB, speeds review process, May involved a small amount of physical or psychological risk

A

Expedited study

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15
Q

Study with the highest amount of risk, receive full review by IRB, studies were a special population has a risk of harm

A

Full review studies

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