Chapter 4: Ethics in Research Flashcards

1
Q

What 5 changes were made in the Milgram “Authority” experiment?

A

1) stopped treatment at the 150V mark
2) used a screening process to not select people who will have severely negative reactions to the experiment
3) participants were told at least 3 times that they could withdraw from the study at any time
4) administering a sample shock to participants (with consent) to see what they were doing to the actor
5) debriefing immediately after the experiment.

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2
Q

name 4 responsibilities of researchers in terms of maintaining the integrity of the discipline of science

A

1) maintain honesty
2) report scientific research
3) give appropriate credit
4) consider how knowledge obtained in their study should be used.

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3
Q

2 basic categories of ethical responsibility

A

1) responsibility to ensure the welfare and dignity of individuals
2) responsibility to the discipline of science to remain honest and accurate in reporting their research

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4
Q

ethical principles dictate that the ____ invasive but most accurate measurement instruments should be used

A

the least invasive.

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5
Q

Name 5 things that ethical principles dictate

A

1) what measurement instruments should be used
2) how data should be analyzed
3) how data should be reported
4) what research strategies could be used
5) what research designs could be used
6) what individuals should be selected for a study

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6
Q

the ___ ___ Board reviews research involving humans

A

the institutional review board

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7
Q

the _________ committee reviews research involving non humans

A

institutional animal care and use committee reviews research involving non humans

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8
Q

When do the review boards review the ethics of research?

A

BEFORE the research begins. not after the research was done

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9
Q

what year did research committees begin establishing research ethics on human participants?

A

after WWII when they realized the Nazis committed horrible war crimes

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10
Q

Nuremberg Code

A

10 guidelines for ethical treatment of HUMAN participants in research

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11
Q

declaration of helinski

A

medical research involving humans

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12
Q

What are the 3 basic principles of the Belmont Report

A

1) respect: individuals should content to participate
2) beneficience: no harm should be done –> minimize harm and maximize benefits
3) justice: fairness in procedures for selecting participants

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13
Q

most important guideline of the APA guidelines. What code are the APA guidelines similar to?

A

1) DO NO HARM: protect from any unnecessary physical and psychological harm
- if there is any risk, it has to be justified.
- participants must be informed

The APA guidelines are similar to the Nuremberg code guidelines

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14
Q

The ethical responsibility of the clinician to provide the best treatment to the participants is called ____-

A

clinical equipose.

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15
Q

if an experimenter is testing effectiveness of drugs and he gives some people the best drug and others a drug that isn’t as good, which principle is being violated?

A

the do no harm principle

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16
Q

3 main aspects of major ethical issues

A

1) informed consent
2) debriefing
3) confidentiality

17
Q

3 components of informed consent

A

1) information: need to give people information about the experiment
- sometimes you might need to use deception if fully informing them before the experiment would alter the results

2) understanding: make sure participants understand what you are doing.
3) voluntary participation: researchers need to ensure they are not intimidating the volunteers into saying yes. participants need to make the decision to participate in the study based on their own free will

18
Q

what should a person know before volunteering for a study?

A

1) the researcher and the insitution they belong to
2) title of study
3) overall purpose of the study
4) description of what’s involved
5) risks
6) any benefits for participating
7) if results will be confidential
8) assurance that you could refuse to participate at any time, or void your scores
9) contact information
10) reimbursement

19
Q

criteria you must fulfill to be allowed to use deception in the research design

A

1) it must be necessary
2) you cannot hide information from the participant that is expected to cause extreme physical and severe emotional pain.

20
Q

passive deception

A

omission and withholding information (secrets)

21
Q

active deception

A

lying or presenting false information

22
Q

after an experiment that involves deception, you must ___

A

debrief and dehoax the experiments

23
Q

dehoaxing

A

explaining the true purpose of the experiment

24
Q

destabilizing

A

the act of trying to reduce any stressors that may have been caused during the experiment

25
Q

to ensure anonymity and confidentiality, _______ for the group of participants are taken

A

averages. in multi-person studies, you don’t know the scores belonging to each specific individual person

26
Q

Who makes up the IRB?

A

Institutional Review Board is made up of scientists and non scientists

27
Q

IRB criteria

A

1) minimization of risks to participants
2) reasonable risks in relation to benefit
3) equitable selection
4) informed consent
5) documentation of informed consent
6) data monitoring
7) privacy and confidentiality

28
Q

Who makes up the IACUC?

A

the institutional animal care and use committee consists of veterinarians, scientists and members of the public

29
Q

the IACUC is like the IRB but it includes ____

A

it assesses the general care and maintenance of the animal facilities
- looks at animal husbandry, sanitation of housing etc.

30
Q

What is fraud

A

the explicit effort to falsify or misrepresent data

31
Q

why do many scientists turn to fraud

A

publish or perish

32
Q

how does the science committee work to reduce fraud

A

1) replication of studies

2) peer reviewing

33
Q

4 blatant forms of fraudulent data

A

1) researcher fabricates data (doesn’t collect all the data)
2) data is collected but is altered to make things clear in favour of the researchers beliefs
3) missing data is guessed at to have a complete set of data
4) study is suppressed/ not published because it came out the wrong way

34
Q

plagiarism

A

deliberately taking ideas or data from someone else and claiming them as ones own (even if cited)

35
Q

3 parts to informed consent

A

1) information: pts must know what is happening in the experiment
2) understanding: they must understand what is happening
3) voluntary participation: no coercion