390 EXAM 2 Flashcards

1
Q

o Protection of participants’ confidentiality such that even the researcher cannot link individuals with the data they provided

A

anonymity

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2
Q

o The affirmative agreement of member of a vulnerable group (children) to participate in a study

A

assent

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3
Q

o Provided a model for many guidelines adopted by disciplinary organizations in the United States

A

belmont report

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4
Q

o An ethical principle that seeks to maximize benefits for study participants, and prevent harm

A

beneficience

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5
Q

o Allows researchers to refuse to disclose information on study participants in any civil, criminal, administrative, or legislative proceeding

A

ϖ Certificate of Confidentiality

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6
Q

o The fundamental ethical principles established by a discipline or institution to guide researchers’ conduct in research with human (or animal) study participants

A

ϖ Code of Ethics

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7
Q

o Document signed by participants that includes information about the study purpose, specific expectations regarding participation, the voluntary nature of participation, and potential costs and benefits

A

ϖ Consent Form

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8
Q

o Is a pledge that any information participants provide will not be publicly reported in a manner that identifies them and will not be made accessible to others

A

confidentiality

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9
Q

o Sessions following data collection so that participants can ask questions or air complaints

A

ϖ Debriefing

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10
Q

o A situation in which the rights of study participants are in direct conflict with requirements of a study

A

ϖ Ethical Dilemma

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11
Q

o Means that the researcher has fully described the study, the persons right to refuse participation, and possible risk and benefits

A

full disclosure

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12
Q

o The return of a completed questionnaire reflects the person’s voluntary consent to participate

A

implied consent

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13
Q

o Means that participants have adequate information about the study, comprehend the information, and have the power of free choice, enabling them to consent to or decline participation voluntarily

A

informed consent

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14
Q

o In the United States, a group of people affiliated with an institution who convene to review proposed and ongoing studies with respect to ethical considerations

A

ϖ Institutional Review Board (IRB)

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15
Q

o Is a risk expected to be no greater than those ordinarily encountered in daily life or during routine tests or procedures

A

minimal risk

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16
Q

o Consent is continuously renegotiated – QUALITATIVE

A

process consent

17
Q

o Is fabrication, falsification, or plagiarism in proposing, conducting, or reviewing research, or in reporting results

A

research misconduct

18
Q

o Designed to evaluate whether the benefits of participating in a study are in line with the cost, be they financial, physical, emotional, or social

A

ϖ Risk/benefit Assessment

19
Q

o Generous monetary incentive

A

stipend

20
Q

o Special groups of people whose rights in studies need special protection because of their inability to provide meaningful informed consent or because their circumstances place them at higher than average risk of adverse effects (children, unconscious)

A

vulnerable population

21
Q

ϖ Nazi medical experiments
o Most famous example of recent disregard for ethical conduct
o Test human endurance and reactions to untested drugs

A

ϖ Nazi medical experiments

22
Q

why were the Nazi medical experiments unethical

A

♣ Subjects could not refuse to be in study

♣ Were exposed to harm and death

23
Q

o Intentionally infected poor black men with syphilis to see what happened in Alabama.

A

ϖ Tuskegee Syphilis Study

24
Q

♣ Ran by white males
♣ Men were told they were getting access to healthcare by nurse (some is better then none)
♣ There were no informed consent

A

Tuskegee Syphilis Study

25
Q

what did they try to treat the men with during the Tuskegee Syphilis Study?

A

silver

26
Q

o Effected mentally disabled children with hepatitis

o 1950-60s

A

willowbrook

27
Q

o First international set of ethical standards

A

ϖ Nuremberg code

28
Q

o A situation in which the rights of study participants are in direct conflict with requirements of a study
o Violations usually occur out of a researchers conviction that knowledge is potentially life saving or beneficial in the long run

A

ethical dilemma