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Articles

Family Caregivers of Cancer Patients: Perceived Burden and Symptoms During the Early Phases of Cancer Treatment

, MSW, PhD, , PhD, , RN, PhD, , MSW, PhD & , RN, PhD
Pages 289-309 | Received 26 Jun 2013, Accepted 04 Dec 2013, Published online: 14 Mar 2014

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Gunhild M. Gjerset, Cecilie E. Kiserud, Torbjørn Wisløff, Jane B. McCarthy & Lene Thorsen. (2023) Perceived burden and need for support among caregivers of cancer patients. Acta Oncologica 62:7, pages 794-802.
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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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Articles from other publishers (36)

Iben Husted Nielsen, Anders Tolver, Karin Piil, Lars Kjeldsen, Kirsten Grønbæk & Mary Jarden. (2024) Family caregiver quality of life and symptom burden in patients with hematological cancer: A Danish nationwide cross-sectional study. European Journal of Oncology Nursing 69, pages 102538.
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Ayfer Durak & Nezahat Muge Catikkas. (2024) Is caregiver sleep quality an important clinical issue?. Sleep and Biological Rhythms.
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In Seo La, Meg Johantgen, Carla L. Storr, Shijun Zhu, John G. Cagle & Alyson Ross. (2023) Spirituality moderates the relationship between cancer caregiver burden and depression. Palliative and Supportive Care, pages 1-12.
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Kyra Webb, Louise Sharpe, Phyllis Butow, Haryana Dhillon, Robert Zachariae, Nina Møller Tauber, Mia Skytte O’Toole & Joanne Shaw. (2023) Caregiver fear of cancer recurrence: A systematic review and meta‐analysis of quantitative studies. Psycho-Oncology 32:8, pages 1173-1191.
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Mariam Chichua, Chiara Filipponi, Davide Mazzoni & Gabriella Pravettoni. (2023) The emotional side of taking part in a cancer clinical trial. PLOS ONE 18:4, pages e0284268.
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Carolina Posada, Laura Correa, Manuela Castañeda, Mauricio Arias-Rojas & Bertha Tellez. (2023) Relationship Between Adoption of the Caregiver Role and Quality of Life in Caregivers of Cancer Patients Under Active Treatment. The Open Nursing Journal 17:1.
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Zeen Li, Lang Tian, Haiyan Liu, Siyuan Tang & Qirong Chen. (2022) Factors associated with parental burden among parents of children with food allergies in China: a cross-sectional study. BMJ Open 12:9, pages e065772.
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Jennifer Hodgson, Angela Lamson, Irina Kolobova, Emily Tucker, Andrew Brimhall, C. Suzanna Lea & Jason Brinkley. (2021) The Experience of Distress and Coping Among Young Adults with Cancer and Their Caregivers. Contemporary Family Therapy 44:3, pages 199-209.
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Belinda C. Goodwin, Fiona Crawford‐Williams, Michael Ireland, Sonja March, Suzanne K. Chambers, Joanne F. Aitken & Jeff Dunn. (2022) The quality of life of regional and remote cancer caregivers in Australia. European Journal of Cancer Care 31:4.
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Kate M. Gunn, Melanie Weeks, Kristiaan J. J. Spronk, Chloe Fletcher & Carlene Wilson. (2022) Caring for someone with cancer in rural Australia. Supportive Care in Cancer 30:6, pages 4857-4865.
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Yuan-Chien Pan & Yaw-Sheng Lin. (2022) Systematic Review and Meta-Analysis of Prevalence of Depression Among Caregivers of Cancer Patients. Frontiers in Psychiatry 13.
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Tinalipi S Ketlogetswe, Jacoba J Jansen Van Rensburg & Johanna Elizabeth Maree. (2022) The experiences of caregivers of patients living with cancer admitted to a hospice in South Africa. International Journal of Palliative Nursing 28:4, pages 164-171.
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Yanlin Mo, Xiaoying Lai, Ling Li & Yao-zhen Lu. (2022) Sleep, depression, and anxiety in family caregivers of nasopharyngeal carcinoma patients before therapy. Acta Psychologica 223, pages 103504.
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Lisa M Hess, Siew Hoong Wong-Jacobson & Patrick M Peterson. (2021) Health and resource burden of a cancer diagnosis on the caregiver: an analysis of administrative claims data. BMC Health Services Research 21:1.
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Aliny de Oliveira Pedrosa, Daniel de Macêdo Rocha, Aline Costa de Oliveira, Ana Maria Ribeiro dos Santos, Maria do Livramento Fortes Figueiredo & Lídya Tolstenko Nogueira. (2021) Indicadores e fatores associados à sobrecarga em cuidadores informais de pacientes em radioterapia. Acta Paulista de Enfermagem 34.
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Lena J. Lee, Leslie Wehrlen, Gwenyth R. Wallen, Ya Ding & Alyson Ross. (2021) Symptom Clusters and Influencing Factors in Family Caregivers of Individuals With Cancer. Cancer Nursing 44:6, pages E547-E555.
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Inger J. Bergerød, Geir S. Braut, Birte Fagerdal, Bjørnar Gilje & Siri Wiig. (2021) Developing a Next-of-Kin Involvement Guide in Cancer Care—Results From a Consensus Process. Cancer Nursing 44:6, pages E447-E457.
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Nora Lize, Vera IJmker-Hemink, Rianne van Lieshout, Yvonne Wijnholds-Roeters, Manon van den Berg, Maggy Youssef-El Soud, Sandra Beijer & Natasja Raijmakers. (2021) Experiences of patients with cancer with information and support for psychosocial consequences of reduced ability to eat: a qualitative interview study. Supportive Care in Cancer 29:11, pages 6343-6352.
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Winson Fu Zun Yang, Rachael Zhi Yi Lee, Sangita Kuparasundram, Terina Tan, Yiong Huak Chan, Konstadina Griva & Rathi Mahendran. (2021) Cancer caregivers unmet needs and emotional states across cancer treatment phases. PLOS ONE 16:8, pages e0255901.
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Kanjana Thana, Alla Sikorskii, Rebecca Lehto, Charles Given & Gwen Wyatt. (2021) Burden and psychological symptoms among caregivers of patients with solid tumor cancers. European Journal of Oncology Nursing 52, pages 101979.
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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.
Inger Johanne Bergerød, Geir S. Braut & Siri Wiig. (2020) Resilience From a Stakeholder Perspective: The Role of Next of Kin in Cancer Care. Journal of Patient Safety 16:3, pages e205-e210.
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Ch Anterrioti, Victoria Alikari & M Kelesi. (2020) The effect of the burden of patient care with cancer on family caregivers. Progress in Health Sciences 10:1, pages 102-107.
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Tina L Rylee, Sayantani Sarkar, Sarah C Reed, Elbina Rafizadeh & Janice F Bell. (2019) Unmet Needs for Information and Support Among Military Caregivers. Military Medicine 184:11-12, pages e922-e928.
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Valerie A. Francescutti, Allison H. Maciver, Erika Stewart, Nikia Clark, Bianca Marrara, Frances G. Saad-Harfouche & Elisa M. Rodriguez. (2019) Characterizing the Patient Experience of CS/HIPEC Through In-Depth Interviews with Patients: Identification of Key Concepts in the Development of a Patient-Centered Program. Annals of Surgical Oncology 26:4, pages 1063-1070.
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Gunhild M. Gjerset, Mari Tendille, Tone Skaali, Cecilie E. Kiserud, Alv A. Dahl, Saevar B. Gudbergsson & Lene Thorsen. (2019) Gender differences in health status and benefits of a one-week educational programme for caregivers of cancer patients. European Journal of Cancer Care 28:2, pages e12992.
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Joakim Isaksson, Sara Lilliehorn & Pär Salander. (2018) Next of kin's motives for psychosocial consultation— O ncology social workers' perceptions of 54 next of kin cases . Psycho-Oncology 28:1, pages 154-159.
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A. Al-Bahri, M. Al-Moundhri, Z. Al-Mandhari & M. Al-Azri. (2018) The role of patients’ families in treatment decision-making among adult cancer patients in the Sultanate of Oman. European Journal of Cancer Care 27:3, pages e12845.
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Safora Johansen, Milada Cvancarova & Cornelia Ruland. (2018) The Effect of Cancer Patients’ and Their Family Caregivers’ Physical and Emotional Symptoms on Caregiver Burden. Cancer Nursing 41:2, pages 91-99.
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Ann M. Berger, Ellyn E. Matthews & Mark S. Aloia. 2018. The MASCC Textbook of Cancer Supportive Care and Survivorship. The MASCC Textbook of Cancer Supportive Care and Survivorship 53 65 .
Michael T. Halpern, Mallorie H. Fiero & Melanie L. Bell. (2017) Impact of caregiver activities and social supports on multidimensional caregiver burden: analyses from nationally-representative surveys of cancer patients and their caregivers. Quality of Life Research 26:6, pages 1587-1595.
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Eeeseung Byun, Anners Lerdal, Caryl L. Gay & Kathryn A. Lee. (2016) How Adult Caregiving Impacts Sleep: a Systematic Review. Current Sleep Medicine Reports 2:4, pages 191-205.
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Grigorios Kotronoulas, Yvonne Wengström & Nora Kearney. (2016) Alterations and Interdependence in Self-Reported Sleep-Wake Parameters of Patient–Caregiver Dyads During Adjuvant Chemotherapy for Breast Cancer
. Oncology Nursing Forum 43:3, pages 288-301.
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Janelle V Levesque, Sylvie D Lambert, Afaf Girgis, Jane Turner, Patrick McElduff & Karen Kayser. (2015) Do men with prostate cancer and their partners receive the information they need for optimal illness self-management in the immediate post-diagnostic phase?. Asia-Pacific Journal of Oncology Nursing 2:3, pages 169-175.
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Elizabeth R. Kessler, Angela Moss, S. Gail Eckhardt, Mark L. Laudenslager, Kristin Kilbourn, Iris B. Mauss, Daniel W. Bowles, Sharon Hecker, Diane L. Fairclough & Jean S. Kutner. (2014) Distress among caregivers of phase I trial participants: a cross-sectional study. Supportive Care in Cancer 22:12, pages 3331-3340.
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