Consent and assent to participate in research from people with dementia.
about
Presence redefined: The reciprocal nature of engagement between elder-clowns and persons with dementia.Optimizing the mobility of residents with dementia: a pilot study promoting healthcare aide uptake of a simple mobility innovation in diverse nursing home settings.Informed consent to research in long-term care settingsA European study investigating patterns of transition from home care towards institutional dementia care: the protocol of a RightTimePlaceCare studyProcedure versus process: ethical paradigms and the conduct of qualitative research.Feasibility of a web-based dementia feeding skills training program for nursing home staffLiving at the farm, innovative nursing home care for people with dementia - study protocol of an observational longitudinal study.Making the Most of Mealtimes (M3): protocol of a multi-centre cross-sectional study of food intake and its determinants in older adults living in long term care homesThe ethics of conducting research with mental health service users.Ethical and practical challenges in implementing informed consent in HIV/AIDS clinical trials in developing or resource-limited countries.Articulating the strategies for maximising the inclusion of people with dementia in qualitative research studies.Advance consent, critical interests and dementia research.Comfort with proxy consent to research involving decisionally impaired older adults: do type of proxy and risk-benefit profile matter?How Swallow Pressures and Dysphagia Affect Malnutrition and Mealtime Outcomes in Long-Term Care.Cancer and dementia: an exploratory study of the experience of cancer treatment in people with dementia.Safe and inclusive research practices for qualitative research involving people with dementia: A review of key issues and strategies.Informed Consent to Research with Cognitively Impaired Adults: Transdisciplinary Challenges and Opportunities.Including People with Dementia in Research: An Analysis of Australian Ethical and Legal Rules and Recommendations for Reform.Making sense(s) in dementia: a multisensory and motor-based group activity program.Psychosocial Intervention Use in Long-Stay Dementia Care: A Classic Grounded Theory.Change in quality of life of people with dementia recently admitted to long-term care facilities.The importance of moral sensitivity when including persons with dementia in qualitative research.Using a therapeutic companion robot for dementia symptoms in long-term care: reflections from a cluster-RCT.Dementia friendly initiatives: A state of the science review.Changes in caregiver burden and health-related quality of life of informal caregivers of older people with Dementia: evidence from the European RightTimePlaceCare prospective cohort study.Research ethics in global mental health: advancing culturally responsive mental health research.Informed consent, vulnerability and the risks of group-specific attribution.The relation between mood, activity, and interaction in long-term dementia care.Familiar communication partners' facilitation of topic management in conversations with individuals with dementia.Co-production and engagement of people with dementia: The issue of ethics and creative or intellectual copyright.Cognitive predictors of medical decision-making capacity in mild cognitive impairment and Alzheimer's disease.The impact of reminiscence on the quality of life of residents with dementia in long-stay care.Reducing patient distress: a model for dementia care.Including adults with intellectual disabilities who lack capacity to consent in research.People with dementia: capacity to consent to research participation.Person-centredness in direct care workers caring for residents with dementia: Effects of a psycho-educational intervention.Cancer-related information needs and treatment decision-making experiences of people with dementia in England: a multiple perspective qualitative study.Diagnostic accuracy of the Ottawa 3DY and Short Blessed Test to detect cognitive dysfunction in geriatric patients presenting to the emergency department.Effects of a Motor and Multisensory-Based Approach on Residents with Moderate-to-Severe Dementia
P2860
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P2860
Consent and assent to participate in research from people with dementia.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Consent and assent to participate in research from people with dementia.
@en
type
label
Consent and assent to participate in research from people with dementia.
@en
prefLabel
Consent and assent to participate in research from people with dementia.
@en
P2093
P2860
P356
P1433
P1476
Consent and assent to participate in research from people with dementia.
@en
P2093
Dixie Cole
Eileen Jennings
Marlene A Reimer
Susan Slaughter
P2860
P356
10.1177/0969733007071355
P407
P577
2007-01-01T00:00:00Z