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Journal of Gerontological Social Work Volume 57, 2014 - Issue 6-7: Caring for the Caregivers: Future Directions for Growing Needs
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Articles

Living Close to a Person With Cancer: A Review of the International Literature and Implications for Social Work Practice

Una StenbergCenter for Shared Decision Making and Collaborative Care Research and Section for Physiotherapy and Social Medicine, Oslo University Hospital, Oslo, NorwayCorrespondence[email protected]
,
Mirjam EkstedtCenter for Shared Decision Making and Collaborative Care Research, Oslo University Hospital, Oslo, Norway;School of Technology and Health, KTH Royal Institute of Technology, Stockholm, Sweden
,
Mariann OlssonDepartment of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden
&
Cornelia M. RulandCenter for Shared Decision Making and Collaborative Care Research, Oslo University Hospital, Oslo, Norway;Department for Medicine, University of Oslo, Oslo, Norway
Pages 531-555 | Received 14 May 2013, Accepted 06 Jan 2014, Published online: 29 Jul 2014

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Pieter Coenen, Amber D. Zegers, Nadia de Vreeze, Allard J. van der Beek & Saskia F. A. Duijts. (2023) ‘Nobody can take the stress away from me’: a qualitative study on experiences of partners of patients with cancer regarding their work and health. Disability and Rehabilitation 45:10, pages 1696-1704.
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Anita Strøm & Anne Dreyer. (2019) Next of kin’s protracted challenges with access to relevant information and involvement opportunities. Journal of Multidisciplinary Healthcare 12, pages 1-8.
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Ricardo João Teixeira, Allison J Applebaum, Sangeeta Bhatia & Tânia Brandão. (2018) The impact of coping strategies of cancer caregivers on psychophysiological outcomes: an integrative review. Psychology Research and Behavior Management 11, pages 207-215.
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Tracy Wharton & Kara Zivin. (2017) Relationships Among Caregiving, Income, Gender, and Health: A Cross-Sectional Examination of a Representative Sample of Older Americans. Journal of Social Service Research 43:1, pages 141-148.
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Debra J. Sheets, Kathy Black & Lenard W. Kaye. (2014) Who Cares for Caregivers? Evidence-Based Approaches to Family Support. Journal of Gerontological Social Work 57:6-7, pages 525-530.
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Articles from other publishers (13)

Solbjørg Watland, Lise Solberg Nes, Elizabeth Hanson, Mirjam Ekstedt, Una Stenberg & Elin Børøsund. (2023) The Caregiver Pathway, a Model for the Systematic and Individualized Follow-up of Family Caregivers at Intensive Care Units: Development Study. JMIR Formative Research 7, pages e46299.
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Tess Thompson, Maxine Davis, Maria Pérez, Melissa Jonson-Reid & Donna B. Jeffe. (2022) “We’re in This Together”: Perceived Effects of Breast Cancer on African American Survivors’ Marital Relationships. Journal of the Society for Social Work and Research 13:4, pages 789-815.
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In Seo La, Meg Johantgen, Carla L. Storr, Shijun Zhu, John G. Cagle & Alyson Ross. (2021) Caregiver burden and related factors during active cancer treatment: A latent growth curve analysis. European Journal of Oncology Nursing 52, pages 101962.
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Inger Johanne Bergerød. 2021. Quality and safety in hospital cancer care: A mixed methods study of next of kin involvement. Quality and safety in hospital cancer care: A mixed methods study of next of kin involvement.
Mette Stie, Anne-Lisbeth Pedersen, Pia Koustrup, Bodil Winther, Bente Hoeck & Charlotte Delmar. (2020) Ansvarlige, men i anden række – en kritisk diskursanalyse af pårørendeinddragelse. Nordisk sygeplejeforskning 10:3, pages 185-200.
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Ian Banks, David Weller, Mehmet Ungan, Peter Selby, Matti Aapro, Marc Beishon, Marije Bolt, Fiona Bonanno, Claire Champeix, Csaba Dégi, Lisa Jelf Eneqvist, Joanna Kazmierska, Agnieszka Kolacinska, Simon Malas, Sébastien Moine, Danica Rotar Pavlic, Richard Price, Fiona Walter & Lynda Wyld. (2019) ECCO Essential Requirements for Quality Cancer Care: Primary care. Critical Reviews in Oncology/Hematology 142, pages 187-199.
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Inger Johanne Bergerød, Bjørnar Gilje, Geir S. Braut & Siri Wiig. (2018) Next-of-kin involvement in improving hospital cancer care quality and safety – a qualitative cross-case study as basis for theory development. BMC Health Services Research 18:1.
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Theola Potgieter & Johanna E Maree. (2018) The palliative chemotherapy decision and experiences of South African patients and their families. International Journal of Palliative Nursing 24:6, pages 272-280.
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J.E. Maree, D. Moshima, M. Ngubeni & L. Zondi. (2018) On being a caregiver: The experiences of South African family caregivers caring for cancer patients. European Journal of Cancer Care 27:2, pages e12801.
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Nadine Köhle, Constance H. C. Drossaert, Jasmijn Jaran, Karlein M. G. Schreurs, Irma M. Verdonck-de Leeuw & Ernst T. Bohlmeijer. (2017) User-experiences with a web-based self-help intervention for partners of cancer patients based on acceptance and commitment therapy and self-compassion: a qualitative study. BMC Public Health 17:1.
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C. E. Wakefield, J. E. Fardell, E. L. Doolan, D. Drew, R. De Abreu Lourenco, A. L. Young & R. J. Cohn. (2016) Grandparents of children with cancer: Quality of life, medication and hospitalizations. Pediatric Blood & Cancer 64:1, pages 163-171.
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Shu-Ching Chen, Shiuan-Chen Chiou, Chong-Jen Yu, Yun-Hsiang Lee, Wei-Yu Liao, Pei-Yin Hsieh, Sin-Yuan Jhang & Yeur-Hur Lai. (2016) The unmet supportive care needs—what advanced lung cancer patients’ caregivers need and related factors. Supportive Care in Cancer.
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Peeranuch LeSeure & Supaporn Chongkham-ang. (2015) The Experience of Caregivers Living with Cancer Patients: A Systematic Review and Meta-Synthesis. Journal of Personalized Medicine 5:4, pages 406-439.
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