Atac, A., et al. (2005). A Study of the Opinions and Behaviors of Physicians with Regard to Informed Consent and Refusing Treatment. Military Medicine, 170(7), 566-71.

Brudney, D. (2009, Mar./Apr.). Choosing for another: beyond autonomy and best interests. The Hastings Center Report. 39(2), 31-38.

Dickman, R. L. (2000, March). Bending the rules to get a medication. American Family Physician 61 (5), 1563. http://www.aafp.org/afp/2000/0301/p1563.html

Erlen, J. A. (2010). Informed consent: Revisiting the issues. Orthopaedic Nursing, 29(4), 276-80. Retrieved from

Lambert, V., & Glacken, M. (2011). Engaging with children in research: Theoretical and practical implications of negotiating informed consent/assent. Nursing Ethics, 18(6), 781-801. doi: http://dx.doi.org/10.1177/0969733011401122

Miller, F. G., & Wertheimer, A. (2011). The fair transaction model of informed consent: An alternative to autonomous authorization. Kennedy Institute of Ethics Journal, 21(3), 201-18. Retrieved from Waller, B. N., & Repko, R. A. (2008). Informed consent: Good medicine, dangerous side effects. Cambridge Quarterly of Healthcare Ethics, 17(1), 66-74.

Websites

GAO Highlights (2005). Un-compensated Care. Retrieved from http://www.gao.gov/new.items/d05743t.pdf.

Discuss how you would go about seeking the consent of participants.

• What questions would you expect from their parents/guardians?

• How much information should you share with the children?

• Should this type of study involve children given the risks of speeding the progression of the disease?

  DS 2-3 pages Times new roman 12 pt

  Be sure to provide in-text citation(s) and a reference list to support your viewpoints. Please use at least three (3) research sources (not Wikipedia, or fact sheets). Please do so in ALL subsequent submissions.