Gary Naglie
Biographic Data
| ID | 330091 |
|---|---|
| NAME | Gary Naglie |
| GIVEN NAMES | Gary |
| FAMILY NAME | Naglie |
| SIGNATURE | NAGLIE G |
| AFFILIATIONS | University of Toronto |
| ORCID | 0000-0002-6274-0894 |
| VERIFIED | Yes |
| TOTAL WORKS | 14 |
| TOTAL CITATIONS | 91 |
| AUTHOR COUNT | 14 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2002 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 3 |
Role of Objective and Subjective Cognitive Status on the Driving Habits of Older Canadians: A Compass-ND Study
Background Individuals with mild cognitive impairment (MCI) and dementia often engage in self-regulatory driving behaviours, but less is known about individuals with subjective cognitive impairment (SCI), who perceive cognitive decline without objective evidence of it. Objective and Methods This study describes the driving status and habits of older Canadians in the COMPASS-ND data set ( n = 955) across cognitive groups: cognitively unimpaired (C…
Older Drivers Reduced Engagement in Distracting Behaviors Over a Six-Year Period: Findings From the Candrive Longitudinal Study
Drivers in our cohort reduced their engagement in distracting behaviors over the study period. This suggests that older drivers adjust their driving over time, which aligns with age-related theories and models about compensation
Caregivers' decision‐making for health service utilisation across the Alzheimer's disease trajectory
Health and social care services can enhance the community experiences of people with Alzheimer's disease and their caregivers but making decisions about service use is complex. Using a grounded theory methodology, we explored service use decision-making in 40 spousal and adult children caregivers for people with Alzheimer's disease across the caregiving and disease trajectory. Participants' perception of their initial service interactions influen…
Towards a universal model of family centered care: A scoping review
BACKGROUND: Families play an important role meeting the care needs of individuals who require assistance due to illness and/or disability. Yet, without adequate support their own health and wellbeing can be compromised. The literature highlights the need for a move to family-centered care to improve the well-being of those with illness and/or disability and their family caregivers. The objective of this paper was to explore existing models of fam…
Meta-analysis of Driving Cessation and Dementia: Does Sex Matter
A reference set of health utilities for long-term survivors of prostate cancer: Population-based data from Ontario, Canada
Tacit knowledge of caring and embodied selfhood
The tacit knowledge paradigm is gaining recognition as an important source of knowledge that informs clinical decision-making. It is, however, limited by an exclusive focus on knowledge acquired through clinical practice, and a consequent neglect of the primordial and socio-cultural significance of embodied selfhood, precisely what provides the foundational structure of tacit knowledge of caring and facilitates its manifestation. Drawing on findi…
Validating Diagnostic Information on the Minimum Data Set in Ontario Hospital-Based Long-Term Care
BACKGROUND: Over 20 countries currently use the Minimum Data Set Resident Assessment Instrument (MDS) in long-term care settings for care planning, policy, and research purposes. A full assessment of the quality of the diagnostic information recorded on the MDS is lacking. OBJECTIVE: The primary goal of this study was to examine the quality of diagnostic coding on the MDS. STUDY SAMPLE: Subjects for this study were admitted to Ontario Complex Con…
Expressions of Personhood in Alzheimer's Disease: An Evaluation of Research-Based Theatre as a Pedagogical Tool
A growing number of scholars are turning to dramatic performance as an innovative approach to disseminating the results of qualitative research. With an interest in this aesthetic practice, the authors transformed ethnographic research on personhood in Alzheimer's disease into a dramatic production, Expressions of Personhood in Alzheimer's , which was performed at the outset of focus group discussions with health practitioners. In this article, t…
Utility-based Quality of Life Measures in Alzheimer’s Disease
Responsiveness of disease-specific and generic utility instruments in prostate cancer patients
Expressions of personhood in Alzheimer's: Moving From Ethnographic Text to Performing Ethnography
This article discusses the translation of ethnographic research on embodied selfhood in Alzheimer's disease into a dramatic production for nurses and ancillary health care professionals working with persons who are cognitively impaired. The appeal of dramatic performance as an alternative medium for the translation and dissemination of research is that it provides an accessible presentation of research to audiences of diverse disciplinary backgro…
Patient and Community Preferences for Outcomes in Prostate Cancer: Implications for Clinical Policy
BACKGROUND: Preferences, or utilities, for health outcomes are central in prostate cancer decision-making. Utilities can be elicited directly from patients using standard techniques, or indirectly, using questionnaires that incorporate preference weights from community members. OBJECTIVES: To evaluate directly elicited and indirectly elicited (questionnaire-derived, community-weighted) utilities for prostate cancer outcomes and the effects of sex…
Content validity for dementia of three generic preference based health related quality of life instruments
Tacit knowledge of caring and embodied selfhood
The tacit knowledge paradigm is gaining recognition as an important source of knowledge that informs clinical decision-making. It is, however, limited by an exclusive focus on knowledge acquired through clinical practice, and a consequent neglect of the primordial and socio-cultural significance of embodied selfhood, precisely what provides the foundational structure of tacit knowledge of caring and facilitates its manifestation. Drawing on findi…
Expressions of personhood in Alzheimer's: Moving From Ethnographic Text to Performing Ethnography
This article discusses the translation of ethnographic research on embodied selfhood in Alzheimer's disease into a dramatic production for nurses and ancillary health care professionals working with persons who are cognitively impaired. The appeal of dramatic performance as an alternative medium for the translation and dissemination of research is that it provides an accessible presentation of research to audiences of diverse disciplinary backgro…
Expressions of Personhood in Alzheimer's Disease: An Evaluation of Research-Based Theatre as a Pedagogical Tool
A growing number of scholars are turning to dramatic performance as an innovative approach to disseminating the results of qualitative research. With an interest in this aesthetic practice, the authors transformed ethnographic research on personhood in Alzheimer's disease into a dramatic production, Expressions of Personhood in Alzheimer's , which was performed at the outset of focus group discussions with health practitioners. In this article, t…
Caregivers' decision‐making for health service utilisation across the Alzheimer's disease trajectory
Health and social care services can enhance the community experiences of people with Alzheimer's disease and their caregivers but making decisions about service use is complex. Using a grounded theory methodology, we explored service use decision-making in 40 spousal and adult children caregivers for people with Alzheimer's disease across the caregiving and disease trajectory. Participants' perception of their initial service interactions influen…
Content validity for dementia of three generic preference based health related quality of life instruments
Patient and Community Preferences for Outcomes in Prostate Cancer: Implications for Clinical Policy
BACKGROUND: Preferences, or utilities, for health outcomes are central in prostate cancer decision-making. Utilities can be elicited directly from patients using standard techniques, or indirectly, using questionnaires that incorporate preference weights from community members. OBJECTIVES: To evaluate directly elicited and indirectly elicited (questionnaire-derived, community-weighted) utilities for prostate cancer outcomes and the effects of sex…
Utility-based Quality of Life Measures in Alzheimer’s Disease
Responsiveness of disease-specific and generic utility instruments in prostate cancer patients
Expressions of personhood in Alzheimer's: Moving From Ethnographic Text to Performing Ethnography
This article discusses the translation of ethnographic research on embodied selfhood in Alzheimer's disease into a dramatic production for nurses and ancillary health care professionals working with persons who are cognitively impaired. The appeal of dramatic performance as an alternative medium for the translation and dissemination of research is that it provides an accessible presentation of research to audiences of diverse disciplinary backgro…
Expressions of Personhood in Alzheimer's Disease: An Evaluation of Research-Based Theatre as a Pedagogical Tool
A growing number of scholars are turning to dramatic performance as an innovative approach to disseminating the results of qualitative research. With an interest in this aesthetic practice, the authors transformed ethnographic research on personhood in Alzheimer's disease into a dramatic production, Expressions of Personhood in Alzheimer's , which was performed at the outset of focus group discussions with health practitioners. In this article, t…
Validating Diagnostic Information on the Minimum Data Set in Ontario Hospital-Based Long-Term Care
BACKGROUND: Over 20 countries currently use the Minimum Data Set Resident Assessment Instrument (MDS) in long-term care settings for care planning, policy, and research purposes. A full assessment of the quality of the diagnostic information recorded on the MDS is lacking. OBJECTIVE: The primary goal of this study was to examine the quality of diagnostic coding on the MDS. STUDY SAMPLE: Subjects for this study were admitted to Ontario Complex Con…
Tacit knowledge of caring and embodied selfhood
The tacit knowledge paradigm is gaining recognition as an important source of knowledge that informs clinical decision-making. It is, however, limited by an exclusive focus on knowledge acquired through clinical practice, and a consequent neglect of the primordial and socio-cultural significance of embodied selfhood, precisely what provides the foundational structure of tacit knowledge of caring and facilitates its manifestation. Drawing on findi…
A reference set of health utilities for long-term survivors of prostate cancer: Population-based data from Ontario, Canada
Meta-analysis of Driving Cessation and Dementia: Does Sex Matter
Towards a universal model of family centered care: A scoping review
BACKGROUND: Families play an important role meeting the care needs of individuals who require assistance due to illness and/or disability. Yet, without adequate support their own health and wellbeing can be compromised. The literature highlights the need for a move to family-centered care to improve the well-being of those with illness and/or disability and their family caregivers. The objective of this paper was to explore existing models of fam…
Caregivers' decision‐making for health service utilisation across the Alzheimer's disease trajectory
Health and social care services can enhance the community experiences of people with Alzheimer's disease and their caregivers but making decisions about service use is complex. Using a grounded theory methodology, we explored service use decision-making in 40 spousal and adult children caregivers for people with Alzheimer's disease across the caregiving and disease trajectory. Participants' perception of their initial service interactions influen…
Older Drivers Reduced Engagement in Distracting Behaviors Over a Six-Year Period: Findings From the Candrive Longitudinal Study
Drivers in our cohort reduced their engagement in distracting behaviors over the study period. This suggests that older drivers adjust their driving over time, which aligns with age-related theories and models about compensation
Role of Objective and Subjective Cognitive Status on the Driving Habits of Older Canadians: A Compass-ND Study
Background Individuals with mild cognitive impairment (MCI) and dementia often engage in self-regulatory driving behaviours, but less is known about individuals with subjective cognitive impairment (SCI), who perceive cognitive decline without objective evidence of it. Objective and Methods This study describes the driving status and habits of older Canadians in the COMPASS-ND data set ( n = 955) across cognitive groups: cognitively unimpaired (C…
Medicine (9 works) · Psychology (6 works) · Disease (5 works) · Health related quality of life (5 works) · Health Systems, Economic Evaluations, Quality of Life (5 works) · Nursing (5 works) · Gerontology (4 works) · Health Utilities Index (4 works) · Internal Medicine (4 works) · Physical therapy (4 works)