CH5: Ethics in Research Flashcards

1
Q

What serves as the basis for regulations affecting research by the U.S. government?
A) The Nuremberg Code
B) The Declaration of Helsinki
C) The Belmont Report
D) The Code of Ethics of the American Psychological Association

A

C) The Belmont Report

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2
Q

In response to human rights violations, various codes of ethics have been developed. What was developed after Nazi atrocities were made public as an international effort to establish ethical standards?
A) The Nuremberg Code
B) The Declaration of Helsinki
C) The Belmont Report
D) The Code of Ethics of the American Psychological Association

A

A) The Nuremberg Code

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3
Q

What document covers primarily ethical issues for practicing nurses and includes principles that apply to nurse researchers?
A) Code of Ethics for Nurses with Interpretative
Statements
B) Ethical Research Guidelines for Registered
Nurses
C) Ethical Guidelines in the Conduct,
Dissemination, and Implementation of
Nursing Research
D) ICN Code of Ethics for Nurses

A

A) Code of Ethics for Nurses with Interpretative Statements

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4
Q

The Belmont Report articulated broad principles on which standards of ethical conduct in research are based. Which is not considered an ethical principle for protecting study participants in the report?
A) Beneficence
B) Respect for human dignity
C) Informed consent
D) Justice

A

C) Informed consent

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5
Q

What is beneficence?
A) Performance of some good
B) Protection from physical and psychological harm and exploitation
C) Participants right to self-determination
D) Freedom to control their own actions

A

A) Performance of some good

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6
Q

What is justice?
A) Right to fair treatment
B) Protection from physical and psychological harm and exploitation
C) Participants right to self-determination
D) Freedom to control their own actions

A

A) Right to fair treatment

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7
Q

Which ethical principle may be violated if a researcher unobtrusively studies interactions among patients in a psychiatric hospital?
A) Confidentiality
B) Freedom from harm
C) Right to self-determination
D) Right to privacy

A

C) Right to self-determination

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8
Q

What is the safeguard mechanisms by which even the researcher cannot link the participant with the information provided?
A) Confidentiality
B) Anonymity
C) Informed consent
D) Right to privacy

A

B) Anonymity

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9
Q

What provides prospective participants with information needed to make a reasoned decision about participation?
A) Confidentiality
B) Anonymity
C) Informed consent
D) Right to privacy

A

Informed consent

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10
Q

How can confidentiality of study participants
be increased?
A) Avoiding the collection of any identifying
information
B) Avoiding introducing the participants to any
of the research personnel
C) Placing all identifying information on
computer files rather than in manual files
D) Placing all identifying information on manual
files rather than in computer files

A

A) Avoiding the collection of any identifying
information

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11
Q

What is an example of a vulnerable group?
A) Women hospitalized for a mastectomy
B) Members of a senior citizen group
C) People who do not speak English
D) Pediatric clients

A

D) Pediatric clients

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12
Q

What is a major potential risk of research to
participants?
A) Monetary gains
B) Access to a new and potentially beneficial
treatment
C) Opportunity to discuss personal feelings and
experiences with an objective listener.
D) Physical boredom

A

D) Physical boredom

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13
Q

Researchers can often show their respect for
participants—and proactively minimize
emotional risks—by carefully attending to the
nature of the interactions they have with
them. What are debriefing sessions?
A) Discussions with prospective participants to
obtain informed consent
B) Discussions with participants after a study to
explain various aspects of the study
C) Discussions with a human subjects committee
before a study to obtain permission
D) findings will
be shared after data have been analyzed

A

B) Discussions with participants after a study to
explain various aspects of the study

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14
Q

In a qualitative study that involves multiple
contacts between the researcher and study
participants, what can the researcher
negotiate?
A) Implied consent
B) Stipend
C) Process consent
D) Risk/benefit ratio

A

C) Process consent

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15
Q

When is informed consent not obtained?
A) Researcher pays a stipend to study
participants.
B) Researcher collects information covertly.
C) Risk/benefit ratio is low.
D) Study is determined exempt by Institutional
Review Board.

A

B) Researcher collects information covertly.

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16
Q

Most institutions where research is conducted
have formal committees for reviewing
proposed research plans. In the United States,
what will the committee likely be called?
A) Research Ethics Board
B) Institutional Review Board
C) Ethical Advisory Board
D) Human Subject Committee

A

B) Institutional Review Board

17
Q

What is an expedited review?
A) The committee must consist of five members
to carry out the review.
B) Research involving no more than minimal
risk can use this procedure.
C) The researcher must have an affiliation with
an institution.
D) The research is exempt from the review board
process.

A

B) Research involving no more than minimal
risk can use this procedure.

18
Q

What is an important consideration when
nurses choose to use animals as research
subjects?
A) Must obtain informed consent from the
animal’s owner.
B) Recognize that it is more convenient to use an
animal.
C) Recognize that it is less costly to use animals
than humans.
D) Recognize that animals need humane care and
treatment.

A

D) Recognize that animals need humane care and
treatment.

19
Q

When can the researcher omit informed
consent, when existing data from records and/
or specimens are used?
A) The study does not involve an intervention.
B) The researcher is gathering data
anonymously.
C) Health professional students are used as
subjects.
D) The study is gathering data from records over
10 years old.

A

B) The researcher is gathering data
anonymously.

20
Q

Under HIPAA regulations, a covered entity
such as a hospital can disclose individually
identifiable health information from its
records if the patient signs an authorization
granting access. What does this include?
A) Who will receive the information
B) Why they need the information
C) The Social Security number of the patient
D) If the data is not specifically obtained for the
research

A

A) Who will receive the information