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Sharon M Neli

Biographic Data

ID291068
NAMESharon M Neli
GIVEN NAMESSharon M
FAMILY NAMENeli
SIGNATURENELI S M
AFFILIATIONSUniversity of Exeter
ORCID0000-0001-9055-3837
VERIFIEDYes
TOTAL WORKS9
TOTAL CITATIONS27
AUTHOR COUNT9
EDITOR COUNT0
FIRST PUBLICATION YEAR2006
LATEST PUBLICATION YEAR2024
H-INDEX3
  • Positive experiences in dementia care-giving: Findings from the Ideal programme

    Open Access•Charlotte Quinn, Gill Toms et al.•ARTICLE•Ageing and Society•2024•Cited by: 1•References: 52

    There is a growing evidence base that identifying positive experiences in providing care can have a beneficial influence on carer wellbeing. However, there is a need to better understand what carers identify as the positive aspects of care-giving. The aim of this study is to explore the satisfying aspects of providing care to people with dementia. This study utilised Time 1 data from 1,277 carers of people in the mild-to-moderate stages of dement…

  • Living Well” Trajectories Among Family Caregivers of People With Mild-to-Moderate Dementia in the Ideal Cohort

    Open Access•L Clare, Laura D Gamble et al.•ARTICLE•The Journals of Gerontology…•2022•Cited by: 2•References: 4

    The findings indicate the importance of prompt identification of, and support for, caregivers at risk of the declining capability to "live well" and may assist in identifying those caregivers who could benefit most from targeted support

  • Longitudinal Trajectories of Quality of Life Among People With Mild-to-Moderate Dementia: A Latent Growth Model Approach With Ideal Cohort Study Data

    Open Access•L Clare, Laura D Gamble et al.•ARTICLE•The Journals of Gerontology…•2022•Cited by: 4•References: 3

    Understanding individual trajectories can contribute to personalized care planning. Efforts to prevent decline in perceived QoL should primarily target psychological well-being. Efforts to improve QoL for those with poorer QoL should additionally address functional impairment, isolation, and disadvantage related to social structure

  • Future outlook of people living alone with early-stage dementia and their non-resident relatives and friends who support them

    Open Access•J Heaton, Anthony Martyr et al.•ARTICLE•Ageing and Society•2021•Cited by: 3•References: 20

    Little is known about the experiences of people living alone with dementia in the community and their non-resident relatives and friends who support them. In this paper, we explore their respective attitudes and approaches to the future, particularly regarding the future care and living arrangements of those living with dementia. The study is based on a qualitative secondary analysis of interviews with 24 people living alone with early-stage deme…

  • All the world's a stage: Accounting for the dementia experience - insights from the Ideal study

    Open Access•A Hillman, Ian Rees Jones et al.•ARTICLE•Qualitative Research•2020•Cited by: 1•References: 48

    Qualitative dementia research emphasises the importance of recognising the voice of the person with dementia. However, research imbued with a politics of selfhood, whereby individuals are called upon to give coherence to experience and emotion, jars with representations of dementia as a gradual decline in capacity. Moreover, it reinforces an assumption that there is an essential experience that can be accessed through different methods. Drawing o…

  • Protocol for the Ideal-2 longitudinal study: Following the experiences of people with dementia and their primary carers to understand what contributes to living well with dementia and enhances active …

    Open Access•Barbora Šilarova, Sharon M Neli et al.•ARTICLE•BMC Public Health•2018

    IDEAL-2 will provide evidence about the key indicators of, and factors associated with, living well over the course of dementia and how these differ for particular subgroups. It will tell us which combinations of services and support are most beneficial and cost-effective. Moreover, the IDEAL-2 study will gather evidence from under-researched groups of people with dementia, who are likely to have their own distinct perceptions of living well

  • Dualities of dementia illness narratives and their role in a narrative economy

    Open Access•A Hillman, Ian Rees Jones et al.•ARTICLE•Sociology of Health & Illness•2018•Cited by: 16•References: 22

    The concept of 'narrative economies' has recently been proposed as a set of exchange relationships that, through biography and story-telling, facilitate access to resources and act as a source of value. We utilise this concept to inform our analysis of 18 qualitative interviews with five people with dementia and four informal carers. Our participants are members of a pre-existing group of dementia advocates, representing the voices of those livin…

  • Phenomena of awareness in dementia: Heterogeneity and its implications

    Open Access•Ivana S Marková, L Clare et al.•ARTICLE•Consciousness and Cognition•2014

  • Factor Analyses and Score Validity of the Family Emotional Involvement and Criticism Scale in an Adolescent Sample

    Open Access•Sharon M Neli, Sharon M Nelis et al.•ARTICLE•Educational and Psychological…•2006

    The factor structure of the Family Emotional Involvement and Criticism Scale (FEICS) is tested in a sample of Irish adolescents. Participants were 661 adolescents with a mean age of 15.9 years ( SD = 1.26). Interpretation of both the exploratory and confirmatory factor analysis of the FEICS show support for the two-factor structure of the FEICS with a Perceived Criticism scale and an Emotional Involvement scale. The reliabilities of the subscale …

  • Dualities of dementia illness narratives and their role in a narrative economy

    Open Access•A Hillman, Ian Rees Jones et al.•ARTICLE•Sociology of Health & Illness•2018•Cited by: 16•References: 22

    The concept of 'narrative economies' has recently been proposed as a set of exchange relationships that, through biography and story-telling, facilitate access to resources and act as a source of value. We utilise this concept to inform our analysis of 18 qualitative interviews with five people with dementia and four informal carers. Our participants are members of a pre-existing group of dementia advocates, representing the voices of those livin…

  • Longitudinal Trajectories of Quality of Life Among People With Mild-to-Moderate Dementia: A Latent Growth Model Approach With Ideal Cohort Study Data

    Open Access•L Clare, Laura D Gamble et al.•ARTICLE•The Journals of Gerontology…•2022•Cited by: 4•References: 3

    Understanding individual trajectories can contribute to personalized care planning. Efforts to prevent decline in perceived QoL should primarily target psychological well-being. Efforts to improve QoL for those with poorer QoL should additionally address functional impairment, isolation, and disadvantage related to social structure

  • Future outlook of people living alone with early-stage dementia and their non-resident relatives and friends who support them

    Open Access•J Heaton, Anthony Martyr et al.•ARTICLE•Ageing and Society•2021•Cited by: 3•References: 20

    Little is known about the experiences of people living alone with dementia in the community and their non-resident relatives and friends who support them. In this paper, we explore their respective attitudes and approaches to the future, particularly regarding the future care and living arrangements of those living with dementia. The study is based on a qualitative secondary analysis of interviews with 24 people living alone with early-stage deme…

  • Living Well” Trajectories Among Family Caregivers of People With Mild-to-Moderate Dementia in the Ideal Cohort

    Open Access•L Clare, Laura D Gamble et al.•ARTICLE•The Journals of Gerontology…•2022•Cited by: 2•References: 4

    The findings indicate the importance of prompt identification of, and support for, caregivers at risk of the declining capability to "live well" and may assist in identifying those caregivers who could benefit most from targeted support

  • Positive experiences in dementia care-giving: Findings from the Ideal programme

    Open Access•Charlotte Quinn, Gill Toms et al.•ARTICLE•Ageing and Society•2024•Cited by: 1•References: 52

    There is a growing evidence base that identifying positive experiences in providing care can have a beneficial influence on carer wellbeing. However, there is a need to better understand what carers identify as the positive aspects of care-giving. The aim of this study is to explore the satisfying aspects of providing care to people with dementia. This study utilised Time 1 data from 1,277 carers of people in the mild-to-moderate stages of dement…

  • All the world's a stage: Accounting for the dementia experience - insights from the Ideal study

    Open Access•A Hillman, Ian Rees Jones et al.•ARTICLE•Qualitative Research•2020•Cited by: 1•References: 48

    Qualitative dementia research emphasises the importance of recognising the voice of the person with dementia. However, research imbued with a politics of selfhood, whereby individuals are called upon to give coherence to experience and emotion, jars with representations of dementia as a gradual decline in capacity. Moreover, it reinforces an assumption that there is an essential experience that can be accessed through different methods. Drawing o…

  • Factor Analyses and Score Validity of the Family Emotional Involvement and Criticism Scale in an Adolescent Sample

    Open Access•Sharon M Neli, Sharon M Nelis et al.•ARTICLE•Educational and Psychological…•2006

    The factor structure of the Family Emotional Involvement and Criticism Scale (FEICS) is tested in a sample of Irish adolescents. Participants were 661 adolescents with a mean age of 15.9 years ( SD = 1.26). Interpretation of both the exploratory and confirmatory factor analysis of the FEICS show support for the two-factor structure of the FEICS with a Perceived Criticism scale and an Emotional Involvement scale. The reliabilities of the subscale …

  • Phenomena of awareness in dementia: Heterogeneity and its implications

    Open Access•Ivana S Marková, L Clare et al.•ARTICLE•Consciousness and Cognition•2014

  • Protocol for the Ideal-2 longitudinal study: Following the experiences of people with dementia and their primary carers to understand what contributes to living well with dementia and enhances active …

    Open Access•Barbora Šilarova, Sharon M Neli et al.•ARTICLE•BMC Public Health•2018

    IDEAL-2 will provide evidence about the key indicators of, and factors associated with, living well over the course of dementia and how these differ for particular subgroups. It will tell us which combinations of services and support are most beneficial and cost-effective. Moreover, the IDEAL-2 study will gather evidence from under-researched groups of people with dementia, who are likely to have their own distinct perceptions of living well

  • Dualities of dementia illness narratives and their role in a narrative economy

    Open Access•A Hillman, Ian Rees Jones et al.•ARTICLE•Sociology of Health & Illness•2018•Cited by: 16•References: 22

    The concept of 'narrative economies' has recently been proposed as a set of exchange relationships that, through biography and story-telling, facilitate access to resources and act as a source of value. We utilise this concept to inform our analysis of 18 qualitative interviews with five people with dementia and four informal carers. Our participants are members of a pre-existing group of dementia advocates, representing the voices of those livin…

  • All the world's a stage: Accounting for the dementia experience - insights from the Ideal study

    Open Access•A Hillman, Ian Rees Jones et al.•ARTICLE•Qualitative Research•2020•Cited by: 1•References: 48

    Qualitative dementia research emphasises the importance of recognising the voice of the person with dementia. However, research imbued with a politics of selfhood, whereby individuals are called upon to give coherence to experience and emotion, jars with representations of dementia as a gradual decline in capacity. Moreover, it reinforces an assumption that there is an essential experience that can be accessed through different methods. Drawing o…

  • Future outlook of people living alone with early-stage dementia and their non-resident relatives and friends who support them

    Open Access•J Heaton, Anthony Martyr et al.•ARTICLE•Ageing and Society•2021•Cited by: 3•References: 20

    Little is known about the experiences of people living alone with dementia in the community and their non-resident relatives and friends who support them. In this paper, we explore their respective attitudes and approaches to the future, particularly regarding the future care and living arrangements of those living with dementia. The study is based on a qualitative secondary analysis of interviews with 24 people living alone with early-stage deme…

  • Living Well” Trajectories Among Family Caregivers of People With Mild-to-Moderate Dementia in the Ideal Cohort

    Open Access•L Clare, Laura D Gamble et al.•ARTICLE•The Journals of Gerontology…•2022•Cited by: 2•References: 4

    The findings indicate the importance of prompt identification of, and support for, caregivers at risk of the declining capability to "live well" and may assist in identifying those caregivers who could benefit most from targeted support

  • Longitudinal Trajectories of Quality of Life Among People With Mild-to-Moderate Dementia: A Latent Growth Model Approach With Ideal Cohort Study Data

    Open Access•L Clare, Laura D Gamble et al.•ARTICLE•The Journals of Gerontology…•2022•Cited by: 4•References: 3

    Understanding individual trajectories can contribute to personalized care planning. Efforts to prevent decline in perceived QoL should primarily target psychological well-being. Efforts to improve QoL for those with poorer QoL should additionally address functional impairment, isolation, and disadvantage related to social structure

  • Positive experiences in dementia care-giving: Findings from the Ideal programme

    Open Access•Charlotte Quinn, Gill Toms et al.•ARTICLE•Ageing and Society•2024•Cited by: 1•References: 52

    There is a growing evidence base that identifying positive experiences in providing care can have a beneficial influence on carer wellbeing. However, there is a need to better understand what carers identify as the positive aspects of care-giving. The aim of this study is to explore the satisfying aspects of providing care to people with dementia. This study utilised Time 1 data from 1,277 carers of people in the mild-to-moderate stages of dement…

Dementia (8 works) · Psychology (8 works) · Disease (7 works) · Medicine (7 works) · Dementia and Cognitive Impairment Research (6 works) · Developmental psychology (4 works) · Gerontology (4 works) · Health disparities and outcomes (4 works) · Cohort (3 works) · Intergenerational Family Dynamics and Caregiving (3 works)

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