Informed Consent to Human Subject Research: Improving the Process of Obtaining Informed Consent from Mentally Ill Persons

Citation data:

Fordham Urban Law Journal, Vol: 25, Issue: 1, Page: 143

Publication Year:
1997
Usage 1165
Downloads 1147
Abstract Views 18
Repository URL:
http://ir.lawnet.fordham.edu/ulj/vol25/iss1/5
Author(s):
Derrickson, Dorothy
Publisher(s):
FLASH: The Fordham Law Archive of Scholarship and History
Tags:
informed consent; mentally ill; research; clinical research; schizophrenia; Human Rights Law; Law
article description
This Note demonstrates that the federal regulations regarding human subject research must provide more specific guidelines that emphasize the process of obtaining informed consent from persons with mental illnesses. Part I discusses schizophrenia as a case example of mental illness that requires more stringent informed consent standards in human subject research. Part II describes the legal foundations of informed consent to human experimentation and the current federal regulations for human subject research. Part III examines the inadequacy of current federal regulations for mentally ill research subjects and proposes revisions to ensure that mentally ill persons provide adequate informed consent to participate in research. This Note concludes that when the potential subject is a person with schizophrenia, the process of obtaining informed consent should require a conversation between the physician-investigator and the potential subject in the presence of a third party patient advocate.