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Notes in
Ethics of Human Subjects Research
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Last Update
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Published
10/01/2023
Risks in human subjects research→ {{c1::Physical}} harms: side-effects of medications/procedures → {{c2::Social}} harms: society's judgement…
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10/01/2023
{{c1::Common Rule}} is the legislation regulation ethical treatment of human participants that comes from the 1974 {{c2::Belmont Report}}- basic princ…
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10/01/2023
Basic Principles of {{c2::Belmont Report}}1. {{c3::Respect for persons}}: individuals should be treated as autonomous and those without autonomy (chil…
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10/01/2023
Application of Principles of {{c2::Belmont Report}}1. {{c5::Risk/Benefits Assessement}}: expected benefits must far outweight the potential risk of ha…
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10/01/2023
Different end goals for clinical {{c1::research}} and clinical {{c2::practice}}→ clinical {{c1::research}}: create generalizable knowledge that benefi…
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10/01/2023
Ensuring compliance with Belmont Principles1. {{c1::IRB application}}: any research with human participants must be reviewed by an {{c1::institutional…
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10/01/2023
Data sharing and transparency are particularly important with {{c1::time}}-sensitive research
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10/01/2023
The Common Rule explicitly allows for {{c1::broad}} consent for the future use of biospecimens.
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10/01/2023
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10/01/2023
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10/09/2023
Pillars of ethical healthcare:{{c1::Beneficience}} (doing good){{c1::Non-maleficence}} (to do no harm) {{c1::Autonomy}} (giving the patient the f…
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