Dianne Gove
Biographic Data
| ID | 6731872 |
|---|---|
| NAME | Dianne Gove |
| GIVEN NAMES | Dianne |
| FAMILY NAME | Gove |
| SIGNATURE | GOVE D |
| AFFILIATIONS | Alzheimer Europe Luxembourg City Luxembourg |
| ORCID | 0000-0002-4281-3494 |
| VERIFIED | Yes |
| TOTAL WORKS | 6 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 6 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2016 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Is capacity to consent to healthcare a uniformly defined concept? Insights from a document analysis of laws and national guidelines across six European countries
BACKGROUND: Capacity to consent or decision-making capacity to healthcare is a key prerequisite for a valid informed consent. A clear understanding of this concept is important to protect patients' autonomy. Without it, clinical assessments may vary, jeopardising patients' participation in decisions about their care and increasing the risk of delayed, denied or harmful treatment. Despite substantial international debate and reforms concerning nor…
Conducting public involvement in dementia research
Understanding multi‐stakeholder needs, preferences and expectations to define effective practices and processes of patient engagement in medicine development
BACKGROUND: The holistic evolution of patient engagement in medicines development requires a more detailed understanding of the needs of all involved stakeholders, and one that better accounts for the specific needs of some potentially vulnerable patient populations and key stages in medicines development. OBJECTIVE: The purpose of this convergent mixed-methods study was to better understand the needs of different stakeholders concerning patient …
Towards capturing meaningful outcomes for people with dementia in psychosocial intervention research
BACKGROUND: People with dementia are often marginalized and excluded from influence, also in relation to dementia research. There is, however, a growing requirement for inclusion through Patient and Public Involvement (PPI), but there is still limited knowledge on how researchers can fully benefit from the involvement of people with dementia in the development and testing of psychosocial interventions. This paper describes the results of a pan-Eu…
Ethically challenging situations faced by professional carers of people with dementia
Context, aims and objectives: Caring for people with dementia in an ethical manner is not an option but a fundamental component of good care. However, professional carers of people with dementia in care homes and hospital settings sometimes find themselves in situations in which it is hard to decide what, if anything, would be the right thing to do. It is particularly difficult to make such decisions when each possible option seems to be good for…
A comparative analysis of national care pathways for people with dementia living at home in Europe
Introduction: Care pathways chronologically pinpoint the key steps to be taken throughout a person’s care journey. In the case of dementia, the term “care pathway” makes reference to how national systems seek to provide seamless care and treatment from the moment of detection and diagnosis of dementia to end of life. The term also refers to the experiences of people with dementia and their families with such care systems.Methods: The aim of this …
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Ethically challenging situations faced by professional carers of people with dementia
Context, aims and objectives: Caring for people with dementia in an ethical manner is not an option but a fundamental component of good care. However, professional carers of people with dementia in care homes and hospital settings sometimes find themselves in situations in which it is hard to decide what, if anything, would be the right thing to do. It is particularly difficult to make such decisions when each possible option seems to be good for…
A comparative analysis of national care pathways for people with dementia living at home in Europe
Introduction: Care pathways chronologically pinpoint the key steps to be taken throughout a person’s care journey. In the case of dementia, the term “care pathway” makes reference to how national systems seek to provide seamless care and treatment from the moment of detection and diagnosis of dementia to end of life. The term also refers to the experiences of people with dementia and their families with such care systems.Methods: The aim of this …
Towards capturing meaningful outcomes for people with dementia in psychosocial intervention research
BACKGROUND: People with dementia are often marginalized and excluded from influence, also in relation to dementia research. There is, however, a growing requirement for inclusion through Patient and Public Involvement (PPI), but there is still limited knowledge on how researchers can fully benefit from the involvement of people with dementia in the development and testing of psychosocial interventions. This paper describes the results of a pan-Eu…
Conducting public involvement in dementia research
Understanding multi‐stakeholder needs, preferences and expectations to define effective practices and processes of patient engagement in medicine development
BACKGROUND: The holistic evolution of patient engagement in medicines development requires a more detailed understanding of the needs of all involved stakeholders, and one that better accounts for the specific needs of some potentially vulnerable patient populations and key stages in medicines development. OBJECTIVE: The purpose of this convergent mixed-methods study was to better understand the needs of different stakeholders concerning patient …
Is capacity to consent to healthcare a uniformly defined concept? Insights from a document analysis of laws and national guidelines across six European countries
BACKGROUND: Capacity to consent or decision-making capacity to healthcare is a key prerequisite for a valid informed consent. A clear understanding of this concept is important to protect patients' autonomy. Without it, clinical assessments may vary, jeopardising patients' participation in decisions about their care and increasing the risk of delayed, denied or harmful treatment. Despite substantial international debate and reforms concerning nor…
Medicine (5 works) · Psychology (5 works) · Dementia (4 works) · Disease (3 works) · Mental Health and Patient Involvement (3 works) · Nursing (3 works) · Gerontology (2 works) · Health care (2 works) · Political science (2 works) · Public relations (2 works)