The SRA Symposium - College of Medicine

Papers
References
Agre, P., Campbell, F.A., Goldman, B.D., Boccia, M.L., Kass, N., McCullough, L.B., Merz, J.F.,
Miller, S.M., Mintz, J., Rapkin, B., Sugarman, J., Sorenson, J., and Wirshing, D. (2003).
Improving Informed Consent: The Medium is Not the Message. IRB: Ethics and Human Research
Supplement 25(5): S11-S19.
Alliance for Human Research Protection. 2002. Retrieved 3/30/2005 from
.
Appelbaum, P.S., Roth, L.H., Lidz, C.W., Benson, P., and Winslade, W. (1987). False Hopes and
Best Data: Consent to Research and the Therapeutic Misconception. Hastings Center Report
17(2): 20-24.
Beauchamp, T.L., and Childress, J.F. 2001. Principles of Biomedical Ethics. Fifth Edition.
New York: Oxford University Press.
Chambers, T. (1999). The Fiction of Bioethics: Cases as Literary Texts. New York: Routledge.
Charon, R. (1994). Narrative Contributions to Medical Ethics: Recognition, Formulation, Interpretation,
and Validation in the Practice of the Ethicist. In E.R. DuBose, R.P. Hamel, and L.J.
O’Connell (Eds.), A Matter of Principles? Ferment in U.S. Bioethics. (pp. 260-283). Valley
Forge, PA: Trinity Press International.
Coyne, C., Xu, R., Raich, P., Plomer, K., Dignan, M., Wenzel, L.B., Fairclough, D., Habermann,
T., Schnell, L., Quella, S., Cella, D., and the Eastern Cooperative Oncology Group. (2003).
Randomized, Controlled Trial of an Easy-to-Read Informed Consent Statement for Clinical
Trial Participation: A Study of the Eastern Cooperative Oncology Group. Journal of Clinical
Oncology 21: 1836-1842.
Department of Health and Human Services (DHHS). (1991). 45 CFR 46.116 General
Requirements for Informed Consent. 56 FR 28003 (June 18, 1991).
Donchin, A. (2001). Understanding Autonomy Relationally: Toward a Reconfiguration of
Bioethical Principles. Journal of Medicine and Philosophy 26(4): 365-386.
Dresser, R. (2001). When Science Offers Salvation: Patient Advocacy and Research Ethics.
New York: Oxford University Press.
Fan, R., and Tao, J. (2004). Consent to Medical Treatment: The Complex Interplay of Patients,
Families, and Physicians. Journal of Medicine and Philosophy 29(2): 139-148.
Flory, J., Emanuel, E. (2004). Interventions to Improve Research Participants’ Understanding in
Informed Consent Research. Journal of the American Medical Association 292(13): 1593-
1601.
Food and Drug Administration (FDA). (1981). 21CFR 50.20. General Requirements for Informed
Consent. 46 FR 8951 (Jan. 27, 1981, as amended at 64 FR 10942, Mar. 8, 1999).
Frank, A.W. (1995). The Wounded Storyteller: Body, Illness, and Ethics. Chicago: University of
Chicago Press.
32 2005 Symposium Proceedings Book