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  1. Moral duties of parents and nontherapeutic clinical research procedures involving children.Terrence F. Ackerman - 1980 - Journal of Medical Humanities 2 (2):94-111.
    Shared views regarding the moral respect which is owed to children in family life are used as a guide in determining the moral permissibility of nontherapeutic clinical research procedures involving children. The comparison suggests that it is not appropriate to seek assent from the preadolescent child. The analogy with interventions used in family life is similarly employed to specify the permissible limit of risk to which children may be exposed in nontherapeutic research procedures. The analysis indicates that recent writers misconceive (...)
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  • Minors' Assent, Consent, or Dissent to Medical Research.Sanford Leikin - 1993 - IRB: Ethics & Human Research 15 (2):1.
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  • Children in research: new perspectives and practices for informed consent.Marion E. Broome, Eric Kodish, Gail Geller & Laura A. Siminoff - 2003 - IRB: Ethics & Human Research 5 (5):S20 - S23.
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  • Informed Consent: Legal Theory and Clinical Practice.Paul S. Appelbaum, Charles W. Lidz & Alan Meisel - 1987 - Oxford University Press USA.
    Written from the combined perspectives of a physician, lawyer, and social scientist, this book is the first reference work to provide a concise and practical overview of informed consent. Topics include the ethical theories and history of the principle of informed consent, all legal requirements for practitioners, and suggesions for making the interaction between doctor and patient clinically meaningful.
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  • Should children decide whether they are enrolled in nonbeneficial research?David Wendler & Seema Shah - 2003 - American Journal of Bioethics 3 (4):1 – 7.
    The U.S. federal regulations require investigators conducting nonbeneficial research to obtain the assent of children who are capable of providing it. Unfortunately, there has been no analysis of which children are capable of assent or even what abilities ground the capacity to give assent. Why should investigators be required to obtain the positive agreement of some children, but not others, before enrolling them in research that does not offer a compensating potential for direct benefit? We argue that the scope of (...)
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  • Child assent and parental permission in pediatric research.Wilma C. Rossi, William Reynolds & Robert M. Nelson - 2003 - Theoretical Medicine and Bioethics 24 (2):131-148.
    Since children are considered incapable ofgiving informed consent to participate inresearch, regulations require that bothparental permission and the assent of thepotential child subject be obtained. Assent andpermission are uniquely bound together, eachserving a different purpose. Parentalpermission protects the child from assumingunreasonable risks. Assent demonstrates respectfor the child and his developing autonomy. Inorder to give meaningful assent, the child mustunderstand that procedures will be performed,voluntarily choose to undergo the procedures,and communicate this choice. Understanding theelements of informed consent has been theparadigm for (...)
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  • Medical Research with Children: Ethics, Law and Practice.Graham Clayden - 1986 - Journal of Medical Ethics 12 (3):156-157.
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