List of works - Gunn Grande

'It's like trying to ice a cake that's not been baked': a qualitative exploration of the contextual factors associated with implementing an evidence-based information intervention for family carers at the end of life

scientific article published on 20 November 2020

A comparison of strategies to recruit older patients and carers to end-of-life research in primary care

scientific article

A drive for structure: A longitudinal qualitative study of the implementation of the Carer Support Needs Assessment Tool (CSNAT) intervention during hospital discharge at end of life

scientific article published on 03 June 2020

A revised model for coping with advanced cancer. Mapping concepts from a longitudinal qualitative study of patients and carers coping with advanced cancer onto Folkman and Greer's theoretical model of appraisal and coping.

scientific article published on 11 July 2017

A systematic review of instruments related to family caregivers of palliative care patients

scientific article published on 06 July 2010

ADAPTATION, FACE AND CONTENT VALIDATION OF A PALLIATIVE CARE NEEDS ASSESSMENT TOOL FOR PEOPLE WITH INTERSTITIAL LUNG DISEASE

An evaluation of research capacity building from the Cancer Experiences Collaborative

scientific article published on 16 July 2012

Barriers to effective communication across the primary/secondary interface: examples from the ovarian cancer patient journey (a qualitative study).

scientific article

Benefits and challenges of collaborative research: lessons from supportive and palliative care

scientific article

Breaking bad news about transitions to dying: a qualitative exploration of the role of the District Nurse.

scientific article published on 23 September 2014

Caring for the dying: how well prepared are general practitioners? A questionnaire study in Wales

scientific article published in January 2003

Characteristics of the bereavement experience of older persons after spousal loss: An integrative review ⬇️

scientific article published on December 28, 2012

Controlling cancer pain in primary care: the prescribing habits and knowledge base of general practitioners

scientific article

Death at home unlikely if informal carers prefer otherwise: implications for policy

scientific article published on 24 October 2008

Defining patients as palliative: hospital doctors' versus general practitioners' perceptions

scientific article published on 01 May 2002

Development of a Carer Support Needs Assessment Tool (CSNAT) for end-of-life care practice at home: A qualitative study

article

Enabling a family caregiver-led assessment of support needs in home-based palliative care: Potential translation into practice

scientific article published on 20 April 2015

Establishing key criteria to define and compare models of specialist palliative care: A mixed-methods study using qualitative interviews and Delphi survey

scientific article published on 28 June 2019

Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews

scientific article

Exploring differences in referrals to a hospice at home service in two socio-economically distinct areas of Manchester, UK.

scientific article

From ‘conductor’ to ‘second fiddle’: Older adult care recipients’ perspectives on transitions in family caring at hospital admission ⬇️

scientific article published on March 2, 2012

Funding health and social services for older people - a qualitative study of care recipients in the last year of life.

scientific article

General practitioners' and district nurses' views of hospital at home for palliative care

scientific article published in May 2002

How common is medical training in palliative care? A postal survey of general practitioners ⬇️

scientific article published on December 1, 1997

How do patients who participate in cancer support groups differ from those who do not?

scientific article published in April 2006

Improving communication with palliative care cancer patients at home - A pilot study of SAGE & THYME communication skills model.

scientific article

Informal carer bereavement outcome: relation to quality of end of life support and achievement of preferred place of death

scientific article published on 27 February 2009

MORECare research methods guidance development: recommendations for ethical issues in palliative and end-of-life care research

scientific article published on 21 May 2013

Mixed methods research in the development and evaluation of complex interventions in palliative and end-of-life care: report on the MORECare consensus exercise

scientific article

Older Adults' Experiences of Transitions Between Care Settings at the End of Life in England: A Qualitative Interview Study ⬇️

scientific article published on May 31, 2012

Palliative care in hospice and hospital: time to put the spotlight on neglected areas of research

article

Parents’ contrasting views on diet versus activity of children: Implications for health promotion and obesity prevention

article

Place of death and access to home care services: are certain patient groups at a disadvantage?

scientific article published in September 1998

Predicting cancer patients' participation in support groups: a longitudinal study.

scientific article published on 12 May 2014

Prediction of appropriate timing of palliative care for older adults with non-malignant life-threatening disease: a systematic review

scientific article

Psychological morbidity and general health among family caregivers during end-of-life cancer care: A retrospective census survey

article

Psychometric validation of the needs assessment tool: progressive disease in interstitial lung disease

scientific article

Quality of life measures (EORTC QLQ-C30 and SF-36) as predictors of survival in palliative colorectal and lung cancer patients

scientific article

Recommendations for managing missing data, attrition and response shift in palliative and end-of-life care research: part of the MORECare research method guidance on statistical issues

scientific article

Resilience for family carers of advanced cancer patients—how can health care providers contribute? A qualitative interview study with carers

article

School children's own views, roles and contribution to choices regarding diet and activity in Spain.

scientific article published on 13 February 2012

Supporting family caregivers to identify their own needs in end-of-life care: Qualitative findings from a stepped wedge cluster trial.

scientific article published on 2 February 2015

Supporting lay carers in end of life care: current gaps and future priorities.

scientific article published on 20 March 2009

The Adaptation, Face, and Content Validation of a Needs Assessment Tool: Progressive Disease for People with Interstitial Lung Disease.

scientific article

The Carer Support Needs Assessment Tool (CSNAT) for use in palliative and end-of-life care at home: a validation study.

scientific article

The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial

scientific article

The influence of patient and carer age in access to palliative care services

scientific article published in May 2006

The need for new perspectives on evaluation of palliative care

scientific article published on 01 December 2011

The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop

scientific article published on 28 April 2013

Towards better support for family carers: A richer understanding ⬇️

scientific article published on July 1, 2013

What is different about living alone with cancer in older age? A qualitative study of experiences and preferences for care.

scientific article

Which cancer patients are referred to Hospital at Home for palliative care?

scientific article published on 01 March 2002

Who cares for the carers at hospital discharge at the end of life? A qualitative study of current practice in discharge planning and the potential value of using The Carer Support Needs Assessment Tool (CSNAT) Approach

scientific article published in February 2018

Women’s views of consultations about familial risk of breast cancer in primary care

scientific article published on 01 December 2002

List of works by Gunn Grande

'It's like trying to ice a cake that's not been baked': a qualitative exploration of the contextual factors associated with implementing an evidence-based information intervention for family carers at the end of life

A comparison of strategies to recruit older patients and carers to end-of-life research in primary care

A drive for structure: A longitudinal qualitative study of the implementation of the Carer Support Needs Assessment Tool (CSNAT) intervention during hospital discharge at end of life

A revised model for coping with advanced cancer. Mapping concepts from a longitudinal qualitative study of patients and carers coping with advanced cancer onto Folkman and Greer's theoretical model of appraisal and coping.

A systematic review of instruments related to family caregivers of palliative care patients

ADAPTATION, FACE AND CONTENT VALIDATION OF A PALLIATIVE CARE NEEDS ASSESSMENT TOOL FOR PEOPLE WITH INTERSTITIAL LUNG DISEASE

An evaluation of research capacity building from the Cancer Experiences Collaborative

Barriers to effective communication across the primary/secondary interface: examples from the ovarian cancer patient journey (a qualitative study).

Benefits and challenges of collaborative research: lessons from supportive and palliative care

Breaking bad news about transitions to dying: a qualitative exploration of the role of the District Nurse.

Caring for the dying: how well prepared are general practitioners? A questionnaire study in Wales

Characteristics of the bereavement experience of older persons after spousal loss: An integrative review ⬇️

Controlling cancer pain in primary care: the prescribing habits and knowledge base of general practitioners

Death at home unlikely if informal carers prefer otherwise: implications for policy

Defining patients as palliative: hospital doctors' versus general practitioners' perceptions

Development of a Carer Support Needs Assessment Tool (CSNAT) for end-of-life care practice at home: A qualitative study

Enabling a family caregiver-led assessment of support needs in home-based palliative care: Potential translation into practice

Establishing key criteria to define and compare models of specialist palliative care: A mixed-methods study using qualitative interviews and Delphi survey

Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews

Exploring differences in referrals to a hospice at home service in two socio-economically distinct areas of Manchester, UK.

From ‘conductor’ to ‘second fiddle’: Older adult care recipients’ perspectives on transitions in family caring at hospital admission ⬇️

Funding health and social services for older people - a qualitative study of care recipients in the last year of life.

General practitioners' and district nurses' views of hospital at home for palliative care

How common is medical training in palliative care? A postal survey of general practitioners ⬇️

How do patients who participate in cancer support groups differ from those who do not?

Improving communication with palliative care cancer patients at home - A pilot study of SAGE & THYME communication skills model.

Informal carer bereavement outcome: relation to quality of end of life support and achievement of preferred place of death

MORECare research methods guidance development: recommendations for ethical issues in palliative and end-of-life care research

Mixed methods research in the development and evaluation of complex interventions in palliative and end-of-life care: report on the MORECare consensus exercise

Older Adults' Experiences of Transitions Between Care Settings at the End of Life in England: A Qualitative Interview Study ⬇️

Palliative care in hospice and hospital: time to put the spotlight on neglected areas of research

Parents’ contrasting views on diet versus activity of children: Implications for health promotion and obesity prevention

Place of death and access to home care services: are certain patient groups at a disadvantage?

Predicting cancer patients' participation in support groups: a longitudinal study.

Prediction of appropriate timing of palliative care for older adults with non-malignant life-threatening disease: a systematic review

Psychological morbidity and general health among family caregivers during end-of-life cancer care: A retrospective census survey

Psychometric validation of the needs assessment tool: progressive disease in interstitial lung disease

Quality of life measures (EORTC QLQ-C30 and SF-36) as predictors of survival in palliative colorectal and lung cancer patients

Recommendations for managing missing data, attrition and response shift in palliative and end-of-life care research: part of the MORECare research method guidance on statistical issues

Resilience for family carers of advanced cancer patients—how can health care providers contribute? A qualitative interview study with carers

School children's own views, roles and contribution to choices regarding diet and activity in Spain.

Supporting family caregivers to identify their own needs in end-of-life care: Qualitative findings from a stepped wedge cluster trial.

Supporting lay carers in end of life care: current gaps and future priorities.

The Adaptation, Face, and Content Validation of a Needs Assessment Tool: Progressive Disease for People with Interstitial Lung Disease.

The Carer Support Needs Assessment Tool (CSNAT) for use in palliative and end-of-life care at home: a validation study.

The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial

The influence of patient and carer age in access to palliative care services

The need for new perspectives on evaluation of palliative care

The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop

Towards better support for family carers: A richer understanding ⬇️

What is different about living alone with cancer in older age? A qualitative study of experiences and preferences for care.

Which cancer patients are referred to Hospital at Home for palliative care?

Who cares for the carers at hospital discharge at the end of life? A qualitative study of current practice in discharge planning and the potential value of using The Carer Support Needs Assessment Tool (CSNAT) Approach

Women’s views of consultations about familial risk of breast cancer in primary care