Research Ethics and Informed Consent

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PHIL 314 EXAM 1

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19 Terms

1
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Who are vulnerable research groups?

Children, prisoners, the poor, the sick, women, and animals.

2
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What is informed consent?

Knowing and understanding what you're agreeing to.

3
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What makes informed consent hard?

Complicated info, long forms, and legal language.

4
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What are the 5 phases of clinical trials?

Phase 0 (early check), 1 (safety), 2 (effectiveness), 3 (comparison), 4 (long-term study).

5
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What's the difference between research and therapy?

Research finds new knowledge; therapy helps the patient feel better.

6
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Why is using placebos controversial?

It may deceive patients and limit real treatment.

7
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Do most research projects help participants?

No, they mainly aim to get new information.

8
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Why offshore clinical trials?

It's cheaper, but risks consent and safety

9
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What's wrong with consent forms?

They're hard to understand.

10
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What's tricky about children in research?

They can't fully decide for themselves.

11
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Why are prisoners in research controversial?

Consent may not be truly free.

12
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What was wrong with the Tuskegee Syphilis Study?

Deception, no consent, racism, and harm

13
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What's the problem with using bad/immoral research?

It harms trust and may give false results.

14
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Why are the poor and uneducated at risk in research?

Easier to exploit with money or pressure.

15
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What challenges come with terminally ill patients in research?

Desperation and limited time.

16
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What's speciesism?

Prioritizing humans over animals

17
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What's difficult with research on people with disabilities?

Consent and increased risk of harm.

18
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Why were women often excluded from studies?

To avoid pregnancy issues, but it caused lack of research on women's health.

19
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What are the Belmont Report's three ethics rules?

Respect for persons, beneficence (do good), and justice (be fair).