Literature DB >> 21611864

Role recognition and changes to self-identity in family caregivers of people with advanced cancer: a qualitative study.

Anna Ugalde1, Meinir Krishnasamy, Penelope Schofield.   

Abstract

PURPOSE: Family caregivers of people with advanced cancer can provide extensive support to the patient. However, the role is not well defined and their experiences are poorly understood. This study aimed to explore how caregivers view their role and the impact of their caregiving.
METHODS: A symbolic interactionist framework guided the in-depth individual interviews and grounded theory methodology was used to analyse the data. A total of 17 interviews were conducted: 13 with active caregivers and 4 with bereaved caregivers.
RESULTS: Three dominant codes are presented. Caregivers lacked role recognition, as they struggled to recognise their role existed, even though they took on extensive and challenging tasks. Caregivers reported substantial loss or changes to their self-identity: with some caregivers reporting not being able to stop thinking about caregiving and others having difficulty answering questions about themselves. Caregivers also demonstrated difficulty in taking a break: active caregivers did not consider taking a break, whereas bereaved caregivers retrospectively admitted needing a break but reported an inability to take one.
CONCLUSIONS: Caregiving is complex and extensive. People who care for those with advanced cancer are in need of intervention to provide support and assistance to them in their role. However, this needs to be structured with consideration for how caregivers view their role.

Entities:  

Mesh:

Year:  2011        PMID: 21611864     DOI: 10.1007/s00520-011-1194-9

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  34 in total

1.  Working with ambivalence: informal caregivers of patients at the end of life.

Authors:  R Harding; I Higginson
Journal:  Support Care Cancer       Date:  2001-11       Impact factor: 3.603

Review 2.  Part 1: Home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998-2008).

Authors:  Ki Stajduhar; L Funk; C Toye; Ge Grande; S Aoun; Cj Todd
Journal:  Palliat Med       Date:  2010-06-18       Impact factor: 4.762

3.  Patterns of caregiver experiences among partners of cancer patients.

Authors:  C Nijboer; M Triemstra; R Tempelaar; M Mulder; R Sanderman; G A van den Bos
Journal:  Gerontologist       Date:  2000-12

4.  Anxiety, depression, and quality of life in caregivers of patients with cancer in late palliative phase.

Authors:  E K Grov; A A Dahl; T Moum; S D Fosså
Journal:  Ann Oncol       Date:  2005-04-22       Impact factor: 32.976

5.  Identifying the concerns of informal carers in palliative care.

Authors:  S Payne; P Smith; S Dean
Journal:  Palliat Med       Date:  1999-01       Impact factor: 4.762

6.  Family caregivers' sleep loss and depression over time.

Authors:  Patricia A Carter
Journal:  Cancer Nurs       Date:  2003-08       Impact factor: 2.592

7.  The bereavement experience following home-based family caregiving for persons with advanced cancer.

Authors:  Priscilla M Koop; Vicki R Strang
Journal:  Clin Nurs Res       Date:  2003-05       Impact factor: 2.075

8.  Caregiver burden and unmet patient needs.

Authors:  K Siegel; V H Raveis; P Houts; V Mor
Journal:  Cancer       Date:  1991-09-01       Impact factor: 6.860

9.  Positive aspects and challenges associated with caring for a dying relative at home.

Authors:  Peter Hudson
Journal:  Int J Palliat Nurs       Date:  2004-02

10.  Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?

Authors:  Marjolein Gysels; Cathy Shipman; Irene J Higginson
Journal:  BMC Med Ethics       Date:  2008-04-24       Impact factor: 2.652

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  15 in total

1.  Feasibility Testing and Refinement of a Supportive Educational Intervention for Carers of Patients with High-Grade Glioma - a Pilot Study.

Authors:  Georgia K B Halkett; Elizabeth A Lobb; Lisa Miller; Thérèse Shaw; Rachael Moorin; Anne Long; Anne King; Jenny Clarke; Stephanie Fewster; Anna K Nowak
Journal:  J Cancer Educ       Date:  2018-10       Impact factor: 2.037

2.  Variability in spousal perceptions of caregiving and its relationship to older caregiver health outcomes.

Authors:  Wesley B Godfrey; Jeremy B Yorgason; Yue Zhang; Bret L Hicken; Wei Chen; Randall W Rupper
Journal:  J Gen Intern Med       Date:  2018-03-28       Impact factor: 5.128

3.  Understanding the experiences of older caregivers of patients with lung cancer during palliative chemotherapy in China: a qualitative study.

Authors:  Min Xue; Xiaoyun Chen; Haiyan Zhao; Yumei Zhao; Jing Li; Weijuan Chen
Journal:  Support Care Cancer       Date:  2022-06-28       Impact factor: 3.359

4.  Internet-based support for informal caregivers to individuals with head and neck cancer (Carer eSupport): a study protocol for the development and feasibility testing of a complex online intervention.

Authors:  Ylva Tiblom Ehrsson; Birgitta Johansson; Ulrica Langegård; Åsa Cajander; Maria Carlsson; Louise von Essen; Awais Ahmad; Göran Laurell
Journal:  BMJ Open       Date:  2022-05-27       Impact factor: 3.006

5.  Caregivers' information needs and their 'experiences of care' during treatment are associated with elevated anxiety and depression: a cross-sectional study of the caregivers of renal cancer survivors.

Authors:  Devesh V Oberoi; Vicki White; Michael Jefford; Graham G Giles; Damien Bolton; Ian Davis; Ingrid Winship; H Miles Prince; Jeremy Millar; Simon Harrison; Anne Kay; David Hill
Journal:  Support Care Cancer       Date:  2016-05-05       Impact factor: 3.603

6.  A qualitative study on perceptions of changes reported by caregivers of patients in vegetative state and minimally conscious state: the "time gap experience".

Authors:  Venusia Covelli; Milda Cerniauskaite; Matilde Leonardi; Davide Sattin; Alberto Raggi; Ambra Mara Giovannetti
Journal:  ScientificWorldJournal       Date:  2014-11-06

7.  Identifying priorities for cancer caregiver interventions: protocol for a three-round modified Delphi study.

Authors:  Sarah-May Blaschke; Sylvie D Lambert; Patricia M Livingston; Sanchia Aranda; Anna Boltong; Penelope Schofield; Suzanne K Chambers; Meinir Krishnasamy; Anna Ugalde
Journal:  BMJ Open       Date:  2019-02-13       Impact factor: 2.692

8.  Carers of patients with high-grade glioma report high levels of distress, unmet needs, and psychological morbidity during patient chemoradiotherapy.

Authors:  Anne Long; Georgia K B Halkett; Elizabeth A Lobb; Thérèse Shaw; Elizabeth Hovey; Anna K Nowak
Journal:  Neurooncol Pract       Date:  2015-10-15

9.  Protocol for the Care-IS Trial: a randomised controlled trial of a supportive educational intervention for carers of patients with high-grade glioma (HGG).

Authors:  Georgia K B Halkett; Elizabeth A Lobb; Lisa Miller; Jane L Phillips; Thérése Shaw; Rachael Moorin; Anne Long; Anne King; Jenny Clarke; Stephanie Fewster; Peter Hudson; Meera Agar; Anna K Nowak
Journal:  BMJ Open       Date:  2015-10-26       Impact factor: 2.692

10.  Development of Measure Yourself Concerns and Wellbeing for informal caregivers of people with cancer-a multicentred study.

Authors:  Rachel Jolliffe; Nicole Collaco; Helen Seers; Chris Farrell; Michael J Sawkins; Marie J Polley
Journal:  Support Care Cancer       Date:  2018-09-11       Impact factor: 3.603

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