Bibliography

Selected Bibliography

Advisory Committee on Human Radiation Experiments. The Human Radiation Experiments. New York: Oxford University Press, Inc., 1996.

Beauchamp T, Childress J. Principles of Biomedical Ethics. Third Edition. New York: Oxford University Press, Inc., 1989.

Buchanan A, Brock D. Deciding for Others: The Ethics of Surrogate Decision Making. New York and Cambridge: Cambridge University Free Press, 1995.

Bursztajn H, Feinbloom R, Hamm R, et al. Medical Choices, Medical Chances: How Patients, Families, and Physicians Can Cope with Uncertainty. New York: Free Press, 1984.

Davis T, Holcombe R, Berkel H, et al. Informed consent for clinical trials: A comparative study of standard versus simplified forms. JNCI 1998;90:668­74.

Doak C, Doak L, Root J. Teaching Patients with Low Literacy Skills. Second Edition. New York: Lippincott, 1996.

Doak L, Doak C, Meade C. Strategies to improve cancer education materials. Onc Nursing Forum, 1996;23:1305­12.

Doak C, Doak L, Friedell G, et al. Improving comprehension for cancer patients with low literacy skills: Strategies for clinicians. CA-A Can J for Clinicians 1998;48:151­62.

Dworkin G. Autonomy and informed consent. The Theory and Practice of Autonomy. New York: Cambridge University Press, 1988.

Engelhardt T. The Foundations of Bioethics. Oxford: Oxford University Press, Inc., 1996.

Faden R, Beauchamp T. A History and Theory of Informed Consent. New York: Oxford University Press, Inc., 1986.

Federal Policy For The Protection Of Human Subjects. (Common rule). Federal Register 1991;56:28002.

Freeman W. Making research consent forms informative and understandable: The experience of the Indian Health Service. Camb Q Healthc Ethics 1994;3:512­21.

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Grossman S, Piantadosi S, Covahey C. Are informed consent forms that describe clinical oncology research protocols readable by most patients and their families? J Clin Oncology 1994;12:2211­5.

Hochhauser M. Some overlooked aspects of consent form readability.IRB: A Review Of Human Subjects Research 1997;19:5­9.

Joseph R. Viewpoints and concerns of a clinical trial participant. Cancer 1994;74:2692­3.

Katz J. Experimentation with Human Beings. New York: Russell Sage Foundation, 1972.

Katz J. The Silent World of Doctor and Patient. New York: Free Press, Macmillan Inc., 1984.

Levine R. Ethics and Regulation of Clinical Research. New Haven and London: Yale University Press, 1998.

Meade C, Howser D. Consent forms: How to determine and improve their readability. Onc Nursing Forum 1992;19:1523­8.

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Porter J. Basic considerations in informed consent in research. Clinical Research and Regulatory Affairs 1995;12:95­109.

Savulescu J, Momeyer R. Should informed consent be based on rational beliefs? J Med Ethics 1997;23:282­8.

Schafer A. The ethics of the randomized clinical trial. N Engl J Med 1982;307:719­24.

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Titus S, Keane M. Do you understand? An ethical assessment of researchers' description of the consenting process. J Clin Ethics 1996;7:60­8.

Vanderpool H, ed. The Ethics Of Research Involving Human Subjects: Facing the 21st Century. Frederick, MD: University Publishing Group, 1996.

Veatch R. The Patient as Partner: A Theory of Human Experimentation Ethics. Bloomington and Indianapolis: Indiana University Free Press, 1987.

Veatch R, ed. Medical Ethics. Second Edition. Sudbury, MA: Jones and Bartlett Publishers, 1997.

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