chapter 15 Flashcards

(29 cards)

1
Q

Ethics in the history of psychology - video

A

Watson
monster study
milgram experiment
bystander effect
zimbardo
ash

(see notes)

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2
Q

Three approaches to ethical decisions:

A

deontology
ethical skepticism
Utilitarian

Guidelines enforced by the APA and federal government are primarily utilitarian

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3
Q

Deontology

A

ethics must be judged in light of a universal moral code

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4
Q

Ethical skepticism

A

concrete and inviolate moral codes cannot be formulated

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5
Q

Utilitarian

A

judgements regarding the ethics of a particular action depend on the consequences of the action

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6
Q

Researchers’ Two Obligations

A
  1. To provide information that enhances our understanding of behavioral process and leads to improvement of human or animal welfare
  2. To protect the rights and welfare of the human and nonhuman participants that they study
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7
Q

Cost-Benefit Analysis
(potential benefits)

A

Basic knowledge (e.g., improve theory)

Improvement of research or assessment techniques (e.g., develop new scales)

Practical outcomes (e.g., solving problems)

Benefits for researchers (e.g., professional benefits)

Benefits for research participants (e.g., improve well-being/awareness/skills)

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8
Q

Cost-Benefit Analysis
(potential costs)

A

Time and effort of participants

Participants’ mental and physical welfare

Money

Deception; creation of climate of distrust

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9
Q

Institutional Review Board (IRB)

A

Members are from both scientific and nonscientific disciplines – at least one member must be from the community

Researchers submit a written proposal describing the purpose, procedures, and potential risks of the study

IRB must approve the proposal before the study may be conducted

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10
Q

Informed Consent

A

Inform participants of the nature of their participation in the study and obtain their explicit agreement to participate

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11
Q

Problems with obtaining informed consent:

A

Compromising the validity of the study

Participants who are unable to give informed consent

Ludicrous cases of informed consent

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12
Q

Elements of an Informed Consent Form

A
  1. Description of why the study is being conducted
  2. List of activities that participant will do
  3. Description of possible risks
  4. Statement informing participants that they may refuse to participate with no penalty
  5. Confidentiality statement
  6. Instructions on how to contact the researcher
  7. Signature lines of the researcher and the participant
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13
Q

Coercion to Participate

A

Occurs when participants agree to participate in a research study because of real or implied pressure from some individual who has authority or influence over them

Supervisors, teachers, physicians, managers, and others with ha position of authority should not recruit their subordinates for their research projects

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14
Q

Mental and Physical Stress

A

The focus of a study may require participants to experience pain, stress, failure, anxiety, or other negative emotions

minimal risk

Any use of more than minimal risk requires strong justification

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15
Q

minimal risk

A

risk that is no greater in probability and severity than that ordinarily encountered in daily life or during the performance of routine physical or psychological examinations of tests

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16
Q

Deception

A

misleading or lying to participants for research purposes

17
Q

Types of deception

A
  1. Presenting participants with a false purpose of the study
  2. Using an experimental confederate who poses as another participant or bystander
  3. Providing false feedback to participants
  4. Presenting two related studies as unrelated
  5. Giving incorrect information regarding stimulus materials
18
Q

Objections to Deception

A

Ethical objection
Pragmatic objection
Researchers are not justified in deceiving participants about aspects of the study that might affect their willingness to participate

19
Q

Ethical objection

A

lying and deceit are immoral

20
Q

Pragmatic objection

A

research participants may enter studies suspicious of what the researcher tells them; participants may come to distrust scientists and the research process

21
Q

Goals of Debriefing

A
  1. Clarify the nature of the study for participants
  2. Remove stress or other negative consequences induced by the study
  3. Obtain participants’ reactions to the study itself
  4. Give participants they sense that their participation was important
22
Q

Confidentiality
(slide)

A

Participants have they right to decide when, where, to whom, and to what extent his or her responses will be revealed

confidentiality

The easiest way to maintain confidentiality is to ensure that participants’ responses are anonymous

23
Q

Confidentiality

A

a participant’s data may be used only for purposes of the research and may not be divulged to others

24
Q

Ethical Principles in Research with Animals

A

Research involving non-human animals must be monitored by a person who is experienced in the care and use of laboratory animals and a veterinarian must be available for consultation

Animals must be housed under healthy and humane conditions

Experimental procedures must minimize discomfort

All students working with nonhuman animals must follow all guidelines

25
scientific misconduct
Questionable research practice such as assuming “ownership” over more than one’s contribution to the study or failing to report findings that are inconsistent with one’s own views Unethical behavior such as sexual harassment, abuse of power, discrimination, or failure to follow government regulations
26
Three categories of scientific misconduct
Fabrication, falsification, and plagiarism
27
fabrication
invention of data or cases
28
falsification
intentional distortion of data or results
29
plagiarism
claiming credit for another's work