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Meeting patients’ spiritual needs during end‐of‐life care: A qualitative study of nurses’ and healthcare professionals’ perceptions of spiritual care training

Journal of clinical nursing, 2019-01, Vol.28 (1-2), p.182-189

2019

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Supporting older people with cancer and life-limiting conditions dying at home: a qualitative study of patient and family caregiver experiences of Hospice at Home care

Journal of advanced nursing, 2016-09, Vol.72 (9), p.2162-2172

2016

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Continuing Bonds With Children and Bereaved Young People: A Narrative Review

Omega: Journal of Death and Dying, 2021-08, Vol.83 (3), p.371-389

2021

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Experiences of dying, death and bereavement in motor neurone disease: A qualitative study

Palliative medicine, 2012-06, Vol.26 (4), p.368-378

2012

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Teaching nurses to teach: A qualitative study of nurses’ perceptions of the impact of education and skills training to prepare them to teach end‐of‐life care

Journal of clinical nursing, 2019-05, Vol.28 (9-10), p.1819-1828

2019

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Resilience to care: A systematic review and meta-synthesis of the qualitative literature concerning the experiences of student nurses in adult hospital settings in the UK

Nurse education today, 2012-08, Vol.32 (6), p.657-664

2012

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The use of digital legacies with people affected by motor neurone disease for continuing bonds: An interpretative phenomenological analysis study

Palliative medicine, 2019-07, Vol.33 (7), p.812-822

2019

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A Qualitative Study Exploring Patient, Family Carer and Healthcare Professionals’ Direct Experiences and Barriers to Providing and Integrating Palliative Care for Advanced Head and Neck Cancer

Journal of palliative care, 2021-04, Vol.36 (2), p.121-129

2021

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Development of the Carers’ Alert Thermometer for Young Carers (CAT-YC) to Identify and Screen the Support Needs of Young Carers: A Mixed Method Consensus Study

Child & adolescent social work journal, 2021-10, Vol.38 (5), p.559-570

2021

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A qualitative study of health care professionals' views and experiences of paediatric advance care planning

BMC palliative care, 2018-07, Vol.17 (1), p.93-93, Article 93

2018

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The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study

Disability and rehabilitation, 2012-01, Vol.34 (3), p.247-256

2012

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Gaining consensus on family carer needs when caring for someone dying at home to develop the Carers' Alert Thermometer (CAT): a modified Delphi study

Journal of advanced nursing, 2016-01, Vol.72 (1), p.227-239

2016

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Supporting family carers providing end-of-life home care: a qualitative study on the impact of a hospice at home service

Journal of clinical nursing, 2015-01, Vol.24 (1-2), p.131-140

2015

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The potential therapeutic value for bereaved relatives participating in research: An exploratory study

Palliative & supportive care, 2016-10, Vol.14 (5), p.479-487

2016

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The personal value of being a palliative care Community Volunteer Worker in Uganda: A qualitative study

Palliative medicine, 2012-07, Vol.26 (5), p.753-759

2012

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Health care professionals' perceptions of a community based ‘virtual ward’ medicines management service: A qualitative study

Research in social and administrative pharmacy, 2018-01, Vol.14 (1), p.69-75

2018

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Undertaking healthcare research with vulnerable populations: lessons to share

Nurse researcher, 2016-05, Vol.23 (5), p.6

Jack, Barbara A

2016

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‘A bridge to the hospice’: The impact of a Community Volunteer Programme in Uganda

Palliative medicine, 2011-10, Vol.25 (7), p.706-715

2011

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Meeting the needs of young adults with life‐limiting conditions: A UK survey of current provision and future challenges for hospices

Journal of advanced nursing, 2018-08, Vol.74 (8), p.1888-1898

2018

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The specification, acceptability and effectiveness of respite care and short breaks for young adults with complex healthcare needs: protocol for a mixed-methods systematic review

BMJ open, 2019-06, Vol.9 (6), p.e030470-e030470

2019

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Supporting home care for the dying: an evaluation of healthcare professionals' perspectives of an individually tailored hospice at home service

Journal of clinical nursing, 2013-10, Vol.22 (19-20), p.2778-2786

2013

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End-of-life care in rural areas: what is different?

Current opinion in supportive & palliative care, 2012-09, Vol.6 (3), p.391

2012

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Short break and emergency respite care: what options for young people with life-limiting conditions?

International journal of palliative nursing, 2016-02, Vol.22 (2), p.57

2016

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Development of the Carers' Alert Thermometer (CAT) to identify family carers struggling with caring for someone dying at home: a mixed method consensus study

BMC palliative care, 2015-05, Vol.14 (1), p.22-22, Article 22

2015

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Social services homecare for people with motor neurone disease/amyotrophic lateral sclerosis: Why are such services used or refused?

Palliative medicine, 2012-03, Vol.26 (2), p.123-131

2012

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Meeting patients’ spiritual needs during end‐of‐life care: A qualitative study of nurses’ and healthcare professionals’ perceptions of spiritual care training

Supporting older people with cancer and life-limiting conditions dying at home: a qualitative study of patient and family caregiver experiences of Hospice at Home care

Continuing Bonds With Children and Bereaved Young People: A Narrative Review

Experiences of dying, death and bereavement in motor neurone disease: A qualitative study

Teaching nurses to teach: A qualitative study of nurses’ perceptions of the impact of education and skills training to prepare them to teach end‐of‐life care

Resilience to care: A systematic review and meta-synthesis of the qualitative literature concerning the experiences of student nurses in adult hospital settings in the UK

The use of digital legacies with people affected by motor neurone disease for continuing bonds: An interpretative phenomenological analysis study

A Qualitative Study Exploring Patient, Family Carer and Healthcare Professionals’ Direct Experiences and Barriers to Providing and Integrating Palliative Care for Advanced Head and Neck Cancer

Development of the Carers’ Alert Thermometer for Young Carers (CAT-YC) to Identify and Screen the Support Needs of Young Carers: A Mixed Method Consensus Study

A qualitative study of health care professionals' views and experiences of paediatric advance care planning

The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study

Gaining consensus on family carer needs when caring for someone dying at home to develop the Carers' Alert Thermometer (CAT): a modified Delphi study

Supporting family carers providing end-of-life home care: a qualitative study on the impact of a hospice at home service

The potential therapeutic value for bereaved relatives participating in research: An exploratory study

The personal value of being a palliative care Community Volunteer Worker in Uganda: A qualitative study

Health care professionals' perceptions of a community based ‘virtual ward’ medicines management service: A qualitative study

Undertaking healthcare research with vulnerable populations: lessons to share

‘A bridge to the hospice’: The impact of a Community Volunteer Programme in Uganda

Meeting the needs of young adults with life‐limiting conditions: A UK survey of current provision and future challenges for hospices

The specification, acceptability and effectiveness of respite care and short breaks for young adults with complex healthcare needs: protocol for a mixed-methods systematic review

Supporting home care for the dying: an evaluation of healthcare professionals' perspectives of an individually tailored hospice at home service

End-of-life care in rural areas: what is different?

Short break and emergency respite care: what options for young people with life-limiting conditions?

Development of the Carers' Alert Thermometer (CAT) to identify family carers struggling with caring for someone dying at home: a mixed method consensus study

Social services homecare for people with motor neurone disease/amyotrophic lateral sclerosis: Why are such services used or refused?

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