Background There is increasing international recognition that populations included in trials
should adequately represent the population treated in clinical practice; however, adults who …

Informed consent is an essential requirement prior to clinical trial participation, however
some 'vulnerable'groups, such as people with cognitive impairments and those in medical …

Background Informed consent is considered a fundamental requirement for participation in
trials, yet obtaining consent is challenging in a number of populations and settings. This may …

Background As the UK population ages, the prevalence of both dementia and cancer will
increase. Family carers of people with dementia who are subsequently diagnosed with …

Research involving adults who lack capacity to consent relies on proxy (or surrogate)
decision making. Proxy decisions about participation are ethically complex, with a disparity …

Background Anticipatory planning in the UK focuses on supporting people who anticipate
periods of impaired capacity to express their wishes about future care through processes …

老年痴呆病人代理决策应用研究进展 Page 1 CHINESE NURSING RESEARCH April,2023 Vol.
37 No. 7 老年痴呆病人代理决策应用研究进展 朱春乐1,张婷1*,兰岚1,黄玉桃2,张玉婷1,周敏1,刘君 …

Anticipatory decision-making instruments–continuing powers of attorney and advance
directives–are increasingly seen as a promising way forward to enhance the autonomy of …

Research is important because it underpins evidence-based care. However, people who
lack capacity to consent are often excluded from research, due partly to ethical concerns and …

The number of people diagnosed with dementia is increasing globally and there is a
necessity to find measures to support their quality of life. This mixed methods research study …