Historical Events In Research NR 283 Chamberlain University-Illinois |
UPDATED Questions with 100% Verified Answers
Question:
Populations at increased risk during research studies include
human subjects with
Answer:
limited ability to make decisions
Question:
Incomplete disclosure without informed consent is not
allowed in research under which ethical principle?
Answer:
Autonomy
Question:
A research study that poses minimal risk to subjects requires
which type of Institutional Review Board (IRB) review?
Answer:
Expedited
Question:
Review the ten guiding principles of The Nuremberg Code
and then complete the sentences.
Answer:
Voluntary consent is required Any experimentation must be
for the greater good of the society . If death or disability is
likely, experimentation should not occur. The risks of
experimentation should never exceed the benefits . Only
qualified professionals should conduct experiments and
should oversee all stages of the process .
Question:
Match the type of research to the correct example.
, Answer:
Therapeutic Research: Clients are enrolled in a study that is
trialing a new medication to treat pediatric cancer.
Nontherapeutic Research: A researcher plans to track
epidemiological information on the long-term effects of
chemotherapy in pediatric clients.
Question:
A researcher plans to study the effects of a new medication on
hypertension. However, only Caucasian males from the
northeast will be recruited to participate in the study. Thus,
researchers are violating which ethical principle?
Answer:
Justice
Question:
Which important document first stated that research on
subjects that are incompetent, physically or mentally
incapable of providing consent, or minor children should only
be conducted when necessary to promote the health of the
representative group?
Answer:
The Belmont Report
Question:
Analyze each proposed research study and decide if the
review requires an exempt, expedited, or full Institutional
Review Board (IRB) review.
Answer:
Exempt: A researcher plans to collect data from an electronic
medical record about client age when experiencing the first
myocardial infarction. A researcher plans to interview nurses
about their perceptions of why medication errors occur. A
UPDATED Questions with 100% Verified Answers
Question:
Populations at increased risk during research studies include
human subjects with
Answer:
limited ability to make decisions
Question:
Incomplete disclosure without informed consent is not
allowed in research under which ethical principle?
Answer:
Autonomy
Question:
A research study that poses minimal risk to subjects requires
which type of Institutional Review Board (IRB) review?
Answer:
Expedited
Question:
Review the ten guiding principles of The Nuremberg Code
and then complete the sentences.
Answer:
Voluntary consent is required Any experimentation must be
for the greater good of the society . If death or disability is
likely, experimentation should not occur. The risks of
experimentation should never exceed the benefits . Only
qualified professionals should conduct experiments and
should oversee all stages of the process .
Question:
Match the type of research to the correct example.
, Answer:
Therapeutic Research: Clients are enrolled in a study that is
trialing a new medication to treat pediatric cancer.
Nontherapeutic Research: A researcher plans to track
epidemiological information on the long-term effects of
chemotherapy in pediatric clients.
Question:
A researcher plans to study the effects of a new medication on
hypertension. However, only Caucasian males from the
northeast will be recruited to participate in the study. Thus,
researchers are violating which ethical principle?
Answer:
Justice
Question:
Which important document first stated that research on
subjects that are incompetent, physically or mentally
incapable of providing consent, or minor children should only
be conducted when necessary to promote the health of the
representative group?
Answer:
The Belmont Report
Question:
Analyze each proposed research study and decide if the
review requires an exempt, expedited, or full Institutional
Review Board (IRB) review.
Answer:
Exempt: A researcher plans to collect data from an electronic
medical record about client age when experiencing the first
myocardial infarction. A researcher plans to interview nurses
about their perceptions of why medication errors occur. A
