Ch 6: Ethics Flashcards

1
Q

Animal rights

A

Guidelines used to protect the rights of animals in the conduct of research

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2
Q

Anonymity

A

The participants identity cannot be discerned, even by the researcher, from his or her individual responses

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3
Q

Assent

A

An aspect of informed consent that pertains to protecting the rights of children as research subjects. Includes: basic understanding by the child of what they will expected to do / what will be done to them, purpose of research, preference regarding participation.

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4
Q

Beneficence

A

The obligation to do no harm and maximize possible benefits. Efforts are made to secure well-being.

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5
Q

Benefits

A

Potential positive outcomes of participation in a research study

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6
Q

Confidentiality

A

The individual identities of participants will not be linked to the information they provide and will not be publicly divulged.

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7
Q

Consent

A

Agreement to participate in a study

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8
Q

Ethics

A

The theory or discipline dealing with principles of moral values and moral conduct.

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9
Q

Informed consent

A

Legal principle that requires a researcher to inform individuals about the potential benefits and risks of a study before individuals can participate voluntarily. Must be given without manipulation, undue influence, or coercion.

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10
Q

Justice

A

Subjects should be treated fairly. An injustice occurs when benefit to which a person is entitled is denied without good reason or when a burden is imposed unduly.

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11
Q

Process consent

A

Voluntary continued participation in a study, which can be verbal, for each data-collection point.

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12
Q

Research ethics board

A

Panels that review research projects to assess whether ethical standards are met in relation to the protection of the rights of human participants.

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13
Q

Respect for Persons

A

People have the right to self-determination and to treatment as autonomous agents. They have the freedom to participate or not participate in research. Persons with diminished autonomy are entitled to protection.

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14
Q

Risk-benefit ratio

A

The extent to which the benefits of the study are maximized, and the risks are minimized, so that participants are protected from harm during the study.

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15
Q

Risks

A

The potential negative outcomes of participation in a research study.

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16
Q

Five levels of harm and discomfort

A
  1. No anticipated effects
  2. Temporary discomfort
  3. Unusual level of temporary discomfort
  4. Risk of permanent damage
  5. Certainty of permanent damage
17
Q

Elements of Informed Consent (9)

A
  • Reasonably foreseeable risks, discomforts, benefits
  • Alternative procedures or treatments
  • Confidentiality
  • Compensation for research or injury
  • Who to go to with questions
  • Participants rights
  • Voluntary participation
  • Probability of random assignment
  • Special qualifications of investigator
18
Q

REB Criteria

A

At least 5 members of various backgrounds, both men and women.
At least 2 professionals with relevant experience.
At least 1 participant knowledgeable in ethics.
At least 1 participant knowledgeable in the relevant law.
At least 1 community member unaffiliated with the institution.