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Meaning-making intervention during breast or colorectal cancer treatment improves self-esteem, optimism, and self-efficacy

Social science & medicine (1982), 2006-06, Vol.62 (12), p.3133-3145

2006

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Using Patient- and Family-Reported Outcome and Experience Measures Across Transitions of Care for Frail Older Adults Living at Home: A Meta-Narrative Synthesis

The Gerontologist, 2021-04, Vol.61 (3), p.e23-e38

2021

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Assessing Agreement Between Terminally Ill Cancer Patients’ Reports of Their Quality of Life and Family Caregiver and Palliative Care Physician Proxy Ratings

Journal of pain and symptom management, 2011-09, Vol.42 (3), p.354-365

2011

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How initial policy responses to COVID-19 contributed to shaping dying at home preferences and care provision: key informant perspectives from Canada

BMC health services research, 2023-11, Vol.23 (1), p.1-1330, Article 1330

2023

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Knowledge translation resources to support the use of quality of life assessment tools for the care of older adults living at home and their family caregivers

Quality of life research, 2022-06, Vol.31 (6), p.1727-1747

2022

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Naturalizing dying at home for older adults: A critical analysis of policy texts

Canadian public administration, 2023-12, Vol.66 (4), p.533-555

2023

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Shifts in Homecare Nursing Practices and Their Implications for Families and Clients Receiving Palliative Care at Home

Nursing leadership (Toronto, Ont.), 2023-04, Vol.36 (1), p.75

2023

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‘The beauty and the less beautiful’: exploring the meanings of dying at ‘home’ among community and practitioner representatives and advocates across Canada

Palliative care and social practice, 2023-01, Vol.17, p.26323524231156944-26323524231156944

2023

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More comprehensively measuring quality of life in life-threatening illness: the McGill Quality of Life Questionnaire - Expanded

BMC palliative care, 2019-10, Vol.18 (1), p.92-92, Article 92

2019

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‘I’m only dealing with the acute issues: How medical ward ‘busyness’ constrains care of the dying

Health (London, England : 1997), 2018-09, Vol.22 (5), p.451-468

2018

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Bereaved family members' perceptions of the quality of end-of-life care across four types of inpatient care settings

BMC palliative care, 2017-11, Vol.16 (1), p.59-59, Article 59

2017

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Where would Canadians prefer to die? Variation by situational severity, support for family obligations, and age in a national study

BMC palliative care, 2022-08, Vol.21 (1), p.1-139, Article 139

2022

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How compassionate communities are implemented and evaluated in practice: a scoping review

BMC palliative care, 2022-07, Vol.21 (1), p.1-131, Article 131

2022

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Electronic patient-reported outcomes in clinical kidney practice (ePRO Kidney): a process evaluation of educational support for clinicians

Therapeutic advances in chronic disease, 2023, Vol.14, p.20406223231173624-20406223231173624

2023

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Healing Connections: On Moving from Suffering to a Sense of Well-Being

Journal of pain and symptom management, 2007-04, Vol.33 (4), p.372-388

2007

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The Development and Validation of a Shorter Version of the Canadian Health Care Evaluation Project Questionnaire (CANHELP Lite): A Novel Tool to Measure Patient and Family Satisfaction With End-of-Life Care

Journal of pain and symptom management, 2013-08, Vol.46 (2), p.289-297

2013

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Prolonged grief symptomatology following violent loss: the mediating role of meaning

European journal of psychotraumatology, 2017-01, Vol.8 (sup6), p.1503522-1503522

2017

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Design and introduction of a quality of life assessment and practice support system: perspectives from palliative care settings

Journal of patient-reported outcomes, 2018-08, Vol.2 (1), p.36-36, Article 36

2018

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Legitimising and rationalising in talk about satisfaction with formal healthcare among bereaved family members

Sociology of health & illness, 2012-09, Vol.34 (7), p.1010-1024

2012

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Canada's Compassionate Care Benefit: is it an adequate public health response to addressing the issue of caregiver burden in end-of-life care?

BMC public health, 2011-05, Vol.11 (1), p.335-335, Article 335

2011

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Quality of life and symptom burden in cancer patients admitted to an acute palliative care unit

Journal of palliative care, 2010, Vol.26 (2), p.94-102

2010

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Prolonged Grief and the Disruption of Meaning: Establishing a Mediation Model

Journal of counseling psychology, 2019-11, Vol.66 (6), p.714-725

2019

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Measuring the quality of life of people at the end of life: The McGill Quality of Life Questionnaire–Revised

Palliative medicine, 2017-02, Vol.31 (2), p.120-129

2017

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Helping Them Live Until They Die: Volunteer Practices in Palliative Home Care

Nonprofit and voluntary sector quarterly, 2010-08, Vol.39 (4), p.734-752

2010

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The extra burdens patients in denial impose on their family caregivers

Palliative & supportive care, 2013-04, Vol.11 (2), p.91-99

2013

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