Giving consent in dementia research

The Lancet

Volumn 372, Issue 9634, 2008, Pages 183-185

  Warner, James ^a   Nomani, Erum ^a  

^a ST CHARLES HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; ARTICLE; CANCER PATIENT; CLINICAL ASSESSMENT; COGNITIVE DEFECT; HUMAN; MEDICAL RESEARCH; MENTAL CAPACITY; PRIORITY JOURNAL; RISK ASSESSMENT;

EID: 47149097329     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(08)61049-1     Document Type: Note

References (11)

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3. Warner J., McCarney R., Griffin M., Hill K., and Fisher P. Participation in dementia research: rates and correlates of capacity to give informed consent. J Med Ethics 34 (2008) 167-170
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7. Brodaty H., Dresser R., Eisner M., et al. Alzheimer's Disease International Working Group for Harmonization of Dementia Drug Guidelines for research involving human subjects with dementia. Alzheimer's Dis Assoc Disord 13 (1999) 71-79
8. MRC. MRC ethics guide: medical research involving adults who cannot consent (Nov 13, 2007). http://www.mrc.ac.uk/Utilities/Documentrecord/index.htm?d=MRC004446 (accessed July 10, 2008).
9. Landhuis E. AD research participation: informed consent complicates trials, part 1 (June 30, 2008). http://www.alzforum.org/new/detail.asp?id=1867 (accessed July 9, 2008).
10. Karlawish J., Kim S., Knopman D., van Dyck C., James B., and Marson D. The views of Alzheimer disease patients and their study partners on proxy consent for clinical trial enrollment. Am J Geriatr Psychiatry 16 (2008) 240-247
11. Stocking C., Hougham G., Danner D., Patterson M., Whitehouse P., and Sachs G. Speaking of research advance directives: planning for future research participation. Neurology 66 (2006) 1361-1366