Experiences of family carers of people with cancer receiving home-based end-of-life care services

QR Code

Experiences of family carers of people with cancer receiving home-based end-of-life care services

Aim: To explore family carers experiences and perceptions about formal support services received while caring for people with cancer at home during the last year of life. Background: Cancer is a major leading cause of death globally. Family carers of people with cancer experience significant chal...

Full description

Bibliographic Details
Main Author:	Sharaf, Ahmed Khamis
Format:	Thesis (University of Nottingham only)
Language:	English
Published:	2023
Subjects:	Carers; Terminal illness; Formal support interactions
Online Access:	https://eprints.nottingham.ac.uk/76664/

Similar Items

Supporting family carers in home-based end of life care: using participatory action research to develop a training programme for support workers and volunteers
by: Caswell, Glenys, et al.
Published: (2017)

Caring to the end: exploring the family lives of young people with a parent at the end of life
by: Turner, Nicola
Published: (2016)

Young carers of stroke survivors
by: Cameron, Trudi M.
Published: (2018)

Understanding the burden on palliative care home carers: A phenomenological account
by: Guilfoyle, A., et al.
Published: (2008)

Exploring the experience of communication in the care of children with palliative care needs: the perspectives of nurses, family carers and physicians in Jordan
by: Atout, Maha
Published: (2017)

Continuing to care for people with dementia: Irish family carers' experience of their relative's transition to a nursing home
by: Argyle, Elaine, et al.
Published: (2010)

A profile of known young carers and identification and snapshot of the ones who are hidden.
by: Morrow, Ros
Published: (2005)

Ageing and quality of life in family carers of people with dementia being cared for at home: a literature review
by: de Oliveira, Deborah Cristina, et al.
Published: (2015)

Communication between family carers and health professionals about end-of-life care for older people in the acute hospital setting: a qualitative study
by: Caswell, Glenys, et al.
Published: (2015)

Exploring the process and experiences of nursing care of patients at the end of life: nurses’, patients’, and family carers’ perspectives
by: Khalid, Dalhat Sani
Published: (2019)

How to communicate with patients about future illness progression and end of life: a systematic review
by: Parry, Ruth, et al.
Published: (2014)

Improving health-promoting self-care in family carers of people with dementia: a review of interventions
by: De Oliveira, Deborah, et al.
Published: (2019)

What would most help improve the quality of life of older family carers of people with dementia? A qualitative study of carers’ views
by: Oliveira, D., et al.
Published: (2018)

Effectiveness of Acceptance and Commitment Therapy self-help for carers of people with multiple sclerosis: a feasibility randomised controlled trial
by: Martin, Kristy-Jane
Published: (2018)

Quality of life in informal carers of individuals with multiple sclerosis
by: Topcu, Gogem
Published: (2016)

Coping with and factors impacting upon the experience of lung cancer in patients and primary carers
by: Ellis, J., et al.
Published: (2012)

Palliative care needs of terminally ill people living alone: A service provider perspective
by: Aoun, Samar, et al.
Published: (2012)

The experience of caring for a person with a mental illness: A grounded theory study
by: Wynaden, Dianne
Published: (2007)

Carer experience of back pain is associated with adolescent back pain experience even when controlling for other carer and family factors
by: O'Sullivan, Peter, et al.
Published: (2008)

The Development and Validation of the Dementia Quality of Life Scale for Older Family Carers (DQOL-OC)
by: Oliveira, D.C.
Published: (2017)

Predictors of satisfaction with life in family carers: evidence from the third European quality of life survey
by: De Oliveira, Deborah Christina, et al.
Published: (2016)

Transitioning towards end-of-life care in Jordanian critical care units: health care professionals' perspectives
by: Almansour, Issa Mohammad Ali
Published: (2015)

Carers for older people with co-morbid cognitive impairment in general hospital: characteristics and psychological well-being
by: Bradshaw, Lucy E., et al.
Published: (2012)

An educational intervention to reduce pain and improve pain management for Malawian people living with HIV/AIDS and their family carers: study protocol for a randomised controlled trial
by: Nkhoma, Kennedy, et al.
Published: (2013)

'Doubly deprived': a post-death qualitative study of primary carers of people who died in Western Australia
by: Keesing, Sharon, et al.
Published: (2011)

Communicating with palliative care patients nearing the end of life, their families and carers
by: Archer, Wendy, et al.
Published: (2017)

The Palliative Care Service Enhancement program: specialised palliative care services for people with behaviours and psychological symptoms of dementia in Australia
by: Atee, Mustafa, et al.
Published: (2024)

“It’s Always Been a Second Class Cancer”: An Exploration of the Experiences and Journeys of Bereaved Family Carers of People with Sarcoma
by: O’Connor, M., et al.
Published: (2021)

The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
by: Bentley, B., et al.
Published: (2016)

Dyadic construction of dementia: meta-ethnography and behaviour-process synthesis
by: Bosco, Alessandro
Published: (2018)

Change in carers' activities after the death of their partners
by: Rosenwax, Lorna, et al.
Published: (2013)

Dignity in the terminally ill: revisited
by: Chochinov, H., et al.
Published: (2006)

Review of Community Pharmacy Staff Educational Needs for Supporting Mental Health Consumers and Carers
by: Mey, A., et al.
Published: (2014)

An educational intervention to reduce pain and improve pain related outcomes for Malawian people living with HIV/AIDS and their family carers: a randomised controlled trial
by: Nkhoma, Kennedy Bashan
Published: (2015)

The use of an online support group for neuromuscular disorders: a thematic analysis of message postings
by: Meade, Oonagh, et al.
Published: (2017)

Transition Care in Anorexia Nervosa Through Guidance Online from Peer and Carer Expertise (TRIANGLE): study protocol for a randomised controlled trial
by: Cardi, Valentina, et al.
Published: (2017)

Is dignity therapy feasible to enhance the end of life experience for people with motor neurone disease and their family carers?
by: Bentley, B., et al.
Published: (2012)

Advance care planning: a systematic review about experiences of patients with a life-threatening or life-limiting illness
by: Zwakman, M., et al.
Published: (2018)

Dysexecutive symptoms and carer strain following acquired brain injury: changes measured before and after holistic neuropsychological rehabilitation
by: Goodwin, Rachel A., et al.
Published: (2016)

Is occupation missing from occupational therapy in palliative care?
by: Keesing, Sharon, et al.
Published: (2011)