The views of Alzheimer disease patients and their study partners on proxy consent for clinical trial enrollment.
about
Reactions of persons with dementia to caregivers singing in morning care situations.Using data to improve surrogate consent for clinical research with incapacitated adults.Temporal stability of receptiveness to clinical research on Alzheimer diseaseA randomized, double-blind, placebo-controlled trial of simvastatin to treat Alzheimer disease.Decision making for participation in dementia research.Clinical research risk assessment among individuals with mild cognitive impairmentThe ethics of informed consent in Alzheimer disease research.Older adults' attitudes toward enrollment of non-competent subjects participating in Alzheimer's research.Substitute consent practices in the face of uncertainty: a survey of Canadian researchers in aging.Comfort with proxy consent to research involving decisionally impaired older adults: do type of proxy and risk-benefit profile matter?Stepping out of the shadows of Alzheimer's disease: a phenomenological hermeneutic study of older people with Alzheimer's disease caring for a therapy dog.Operationalising ethical challenges in dementia research-a systematic review of current evidence.Is Safety in the Eye of the Beholder? Safeguards in Research With Adults With Intellectual Disability.Assessment of Capacity to Consent to Research Among Psychiatric Outpatients: Prevalence and Associated Factors.Using nonevidence-based approaches to treat patients with alzheimer's disease.Informed consent, participation in research, and the Alzheimer's patient.Study partners should be required in preclinical Alzheimer's disease trials.Spanish Validation of the MacArthur Competence Assessment Tool for Clinical Research Interview for Assessing Patients' Mental Capacity to Consent to Clinical Research.Can therapy dogs evoke awareness of one's past and present life in persons with Alzheimer's disease?People with dementia: capacity to consent to research participation.Advance directives in dementia research: The opinions and arguments of clinical researchers − an empirical study
P2860
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P2860
The views of Alzheimer disease patients and their study partners on proxy consent for clinical trial enrollment.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
The views of Alzheimer disease ...... for clinical trial enrollment.
@en
The views of Alzheimer disease ...... for clinical trial enrollment.
@nl
type
label
The views of Alzheimer disease ...... for clinical trial enrollment.
@en
The views of Alzheimer disease ...... for clinical trial enrollment.
@nl
prefLabel
The views of Alzheimer disease ...... for clinical trial enrollment.
@en
The views of Alzheimer disease ...... for clinical trial enrollment.
@nl
P2093
P921
P1476
The views of Alzheimer disease ...... for clinical trial enrollment.
@en
P2093
Bryan D James
Christopher H van Dyck
Daniel Marson
Scott Y H Kim
P304
P356
10.1097/JGP.0B013E318162992D
P577
2008-03-01T00:00:00Z