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(Why) should we require consent to participation in research?
1Department of Bioethics, National Institutes of Health, Bethesda, MD 20892.
While coercing participation in biomedical research may be justifiable, a general prohibition is ethically preferred. This approach balances potential benefits against the risks of overriding individual autonomy in research participation.
Area of Science:
- Biomedical Ethics
- Research Ethics
- Moral Philosophy
Background:
- Informed consent is a cornerstone of ethical biomedical research.
- The philosophical underpinnings and justification for informed consent remain debated.
- The ethical permissibility of state-mandated research participation is unclear.
Purpose of the Study:
- To critically examine the ethical justifications for informed consent in biomedical research.
- To explore the moral legitimacy of state-compelled participation in research.
- To propose a framework for evaluating coercive research participation.
Main Methods:
- Philosophical argumentation and ethical analysis.
- Examination of principles such as non-maleficence, bodily integrity, and autonomy.
- Distinction between first-order and second-order moral principles.
Main Results:
- The requirement for informed consent cannot be solely defended by simple ethical principles like autonomy or non-maleficence.
- First-order moral principles may permit, and even justify, state coercion for research participation.
- Second-order moral considerations provide strong reasons for a general prohibition against coercive research participation.
Conclusions:
- While ethically permissible under certain first-order principles, mandatory research participation poses significant ethical challenges.
- A second-order moral prohibition on coercion in research is advisable to protect individuals and maintain public trust.
- Ethical frameworks must carefully balance research imperatives with individual rights and societal values.
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