Cassell, J. A. and Young, A (2002) Why we should not seek individual informed consent for participation in health services research. Journal of Medical Ethics, 28 (5). pp. 313-317. ISSN 0306-6800Full text not available from this repository.
Ethics committees now require that individuals give informed consent to much health services research, in the same way as for clinical research. This is misguided. Existing ethical guidelines do not help us decide how to seek consent in these cases, and have allowed managerial experimentation to remain largely unchecked. Inappropriate requirements for individual consent can institutionalise health inequalities and reduce access to services for vulnerable groups. This undermines the fundamental purpose of the National Health Service (NHS), and ignores our rights and duties as its members, explored here. Alternative forms of community consent should be actively pursued.
|Additional Information:||J Med Ethics|
|Schools and Departments:||Brighton and Sussex Medical School > Brighton and Sussex Medical School|
|Depositing User:||Jackie Cassell|
|Date Deposited:||30 Mar 2007|
|Last Modified:||30 Nov 2012 16:51|
|Google Scholar:||52 Citations|