Gender differences in caregiver burden and its determinants in family members of terminally ill cancer patients
Abstract
OBJECTIVE: Female family caregivers consistently report higher levels of stress and burden compared to male caregivers. Explanations for the apparently higher psychological vulnerability of female caregivers are largely missing to date. This study assesses the correlates and determinants of caregiver burden in family caregivers of advanced cancer patients with a specific focus on gender differences. METHODS: Three hundred and eight self-identified main informal caregivers of advanced cancer patients were cross-sectionally assessed using structured questionnaires for caregiver burden and hypothesised determinants of burden, including sociodemographic characteristics, caring arrangements, support needs, hope and coping style. Gender differences and predictors of burden were assessed using t-tests, chi-squared tests and univariate linear regression. Significant univariate predictors were entered in an analysis of covariance separately for men and women. RESULTS: Burden was significantly higher in women. Hope was the most significant protective factor against burden in both genders, together with perceived fulfilment of support needs. Only in women emotion-oriented coping and being in employment while caring were significantly predictive of higher burden in the multivariate analysis. The model explained 36% of the variance in burden in men and 29% in women. CONCLUSION: Psychological support interventions for family caregivers should take gender-specific risk factors into account. Interventions focusing on keeping up hope while caring for a terminally ill family member may be a valuable addition to palliative services to improve support for family carers. Women may benefit from interventions that address adaptive coping and strategies to deal with the dual demands of employment and caring. Copyright © 2015 John Wiley & Sons, Ltd. Copyright © 2015 John Wiley & Sons, Ltd.
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The role of informal caregiving is mostly assumed by females in a wide array of conditions including advanced cancer.
“the burgeoning recent literature on informal caregiving has highlighted that this role is mostly assumed by females in a wide array of conditions including advanced cancer [28,29,30,31].”
A high number of unmet needs correlate with psychological distress and overall caregiver burden.
“A high number of unmet needs correlate with psychological distress and overall caregiver burden [4].”
From Exploring the Unmet Needs of Cancer Caregivers in India: A Cross-Sectional Survey (2024) · cites this paper as [4]
Cites
Relatives of the Impaired Elderly: Correlates of Feelings of Burden
Zarit, S. H., Reever, K. E., & Bach-Peterson, J. (1980) · The Gerontologist · doi:10.1093/geront/20.6.649 · Cited by 5,810 · see citing works
Positive psychology interventions: a meta-analysis of randomized controlled studies
Bolier, L., Haverman, M., Westerhof, G. J., Riper, H., Smit, F., & Bohlmeijer, E. (2013) · BMC Public Health · doi:10.1186/1471-2458-13-119 · Cited by 1,996 · see citing works
Review of the literature on the effects of caring for a patient with cancer
Stenberg, U., Ruland, C. M., & Miaskowski, C. (2010) · Psycho-Oncology · doi:10.1002/pon.1670 · Cited by 786 · see citing works
Short-form Zarit caregiver burden interviews were valid in advanced conditions
Higginson, I. J., Gao, W., Jackson, D., Murray, J., & Harding, R. (2010) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2009.06.014 · Cited by 343 · cited 1× · see citing works
“ZBI-12) shown to be best suited for the palliative care setting [19,20].”
BackgroundClayton, J. M., Hancock, K. M., Parker, S., Butow, P. N., Walder, S., Carrick, S. E., Currow, D. C., Ghersi, D., Glare, P. A., Hagerty, R. G., et al. (2007) · Psycho-Oncology · doi:10.1002/pon.1288 · Cited by 327 · see citing works
Grov, E. K., Dahl, A. A., Moum, T., & Fosså, S. D. (2005) · Annals of Oncology · doi:10.1093/annonc/mdi210 · Cited by 315 · see citing works
Gender Differences in Caregiving: Why Do Wives Report Greater Burden?
Barusch, A. S., & Spaid, W. M. (1989) · The Gerontologist · doi:10.1093/geront/29.5.667 · Cited by 299 · see citing works
Cancer Caregivers' Quality of Life: Effects of Gender, Relationship, and Appraisal
Kim, Y., Baker, F., & Spillers, R. L. (2007) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2006.11.012 · Cited by 239 · see citing works
Quality of life and mental health in caregivers of outpatients with advanced cancer
Wadhwa, D., Burman, D., Swami, N., Rodin, G., Lo, C., & Zimmermann, C. (2011) · Psycho-Oncology · doi:10.1002/pon.2104 · Cited by 222 · see citing works
Williams, A.-L., & McCorkle, R. (2011) · Palliative & Supportive Care · doi:10.1017/s1478951511000265 · Cited by 193 · see citing works
Duggleby, W., Degner, L. F., Williams, A., Wright, K. E., Cooper, D. M., Popkin, D. R., & Holtslander, L. F. (2007) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2006.09.013 · Cited by 186 · see citing works
Hudson, P., Trauer, T., Kelly, B. J., O’Connor, M., Thomas, K., Zordan, R., & Summers, M. P. (2014) · Psycho-Oncology · doi:10.1002/pon.3610 · Cited by 168 · see citing works
Schrank, B., Brownell, T., Jakaite, Z., Larkin, C., Pesola, F., Riches, S., Tylee, A. T., & Slade, M. (2015) · Epidemiology and Psychiatric Sciences · doi:10.1017/s2045796015000141 · Cited by 163 · see citing works
Self-citationKristjanson, L. J., Atwood, J. R., & Degner, L. F. (1995) · Journal of Nursing Measurement · doi:10.1891/1061-3749.3.2.109 · Cited by 128 · see citing works
Confirmatory factor analysis of a short form of the Coping Inventory for Stressful Situations
Cohan, S. L., Jang, K. L., & Stein, M. B. (2005) · Journal of Clinical Psychology · doi:10.1002/jclp.20211 · Cited by 128 · see citing works
Hudson, P., Trauer, T., Kelly, B. J., O’Connor, M., Thomas, K., Summers, M. P., Zordan, R., & WHITE, V. M. (2013) · Psycho-Oncology · doi:10.1002/pon.3242 · Cited by 107 · see citing works
Development and validation of an integrative scale to assess hope
Schrank, B., Woppmann, A., Sibitz, I., & Lauber, C. (2010) · Health Expectations · doi:10.1111/j.1369-7625.2010.00645.x · Cited by 106 · see citing works
Self-citationKim, Y., van Ryn, M., Jensen, R. E., Griffin, J. M., Potosky, A., & Rowland, J. (2015) · Psycho-Oncology · doi:10.1002/pon.3580 · Cited by 99 · cited 5× · see citing works
“Literature suggests that educating caregivers how to best utilize additional resources for personal emotional support may be beneficial for their individual quality of life especially in women [3].”
BackgroundInfluentialHunt, K. J., Shlomo, N., & Addington-Hall, J. M. (2013) · Palliative Medicine · doi:10.1177/0269216313512012 · Cited by 94 · see citing works
Kang, J., Shin, D. W., Choi, J. E., Sanjo, M., Yoon, S. J., Kim, H. K., Oh, M. S., Kwen, H.-S., Choi, H. Y., & Yoon, W. H. (2012) · Psycho-Oncology · doi:10.1002/pon.3033 · Cited by 91 · see citing works
Effendy, C., Vernooij-Dassen, M. J. F. J., Setiyarini, S., Kristanti, M. S., Tejawinata, S., Vissers, K. C. P., & Engels, Y. (2014) · Psycho-Oncology · doi:10.1002/pon.3701 · Cited by 91 · see citing works
The caregivers’ perspective on the end-of-life phase of glioblastoma patients
Flechl, B., Ackerl, M., Sax, C., Oberndorfer, S., Calabek, B., Sizoo, E. M., Reijneveld, J. C., Crevenna, R., Keilani, M. Y., Gaiger, A., et al. (2013) · Journal of Neuro-Oncology · doi:10.1007/s11060-013-1069-7 · Cited by 87 · see citing works
Giesbrecht, M., Crooks, V. A., Williams, A., & Hankivsky, O. (2012) · International Journal for Equity in Health · doi:10.1186/1475-9276-11-65 · Cited by 78 · see citing works
Wong, W. K. T., Ussher, J. M., & Perz, J. (2009) · Palliative & Supportive Care · doi:10.1017/s1478951509000248 · Cited by 74 · see citing works
Gender differences among Canadian spousal caregivers at the end of life
Brazil, K., Thabane, L., Foster, G., & Bédard, M. (2008) · Health & Social Care in the Community · doi:10.1111/j.1365-2524.2008.00813.x · Cited by 71 · see citing works
Caregivers’ morbidity in palliative care unit: predicting by gender, age, burden and self-esteem
Costa‐Requena, G., Cristòfol, R., & Cañete, J. (2011) · Supportive Care in Cancer · doi:10.1007/s00520-011-1233-6 · Cited by 64 · see citing works
FERRELL, B. R., Hanson, J., & GRANT, M. M. (2012) · Psycho-Oncology · doi:10.1002/pon.3198 · Cited by 60 · see citing works
Gibbons, C., Creese, J., Tran, M., Brazil, K., Chambers, L. A., Weaver, B., & Bédard, M. (2014) · Journal of Women & Aging · doi:10.1080/08952841.2014.854571 · Cited by 54 · see citing works
Caregivers' anxiety and self-efficacy in palliative care
Mystakidou, K., Parpa, E., Panagiotou, I. E., Tsilika, E., Galanos, A., & Gouliamos, A. (2012) · European Journal of Cancer Care · doi:10.1111/ecc.12012 · Cited by 52 · see citing works
Feelings of rewards among family caregivers during ongoing palliative care
Henriksson, A., Goliath, I., & Årestedt, K. (2013) · Palliative & Supportive Care · doi:10.1017/s1478951513000540 · Cited by 47 · see citing works
Improving support for family carers: Key implications for research, policy and practice
Hudson, P. (2013) · Palliative Medicine · doi:10.1177/0269216313488855 · Cited by 46 · see citing works
Young Caregivers in the End-of-Life Setting: A Population-Based Profile of an Emerging Group
Burns, C. M., LeBlanc, T. W., Abernethy, A. P., & Currow, D. C. (2010) · Journal of Palliative Medicine · doi:10.1089/jpm.2010.0004 · Cited by 43 · see citing works
Validation of the Family Inventory of Needs (FIN) for family caregivers in palliative care
Schur, S., Neubauer, M., Amering, M., Ebert‐Vogel, A., Masel, E. K., Sibitz, I., Watzke, H., & Schrank, B. (2014) · Palliative & Supportive Care · doi:10.1017/s1478951514000261 · Cited by 42 · see citing works
Self-citationMacKinnon, C. J. (2009) · Palliative & Supportive Care · doi:10.1017/s1478951509990514 · Cited by 41 · see citing works
Duggleby, W., Williams, A., Holstlander, L., Thomas, R. L., Cooper, D., Hällström, L., Ghosh, S., & O’Rourke, H. M. (2014) · Rural and Remote Health · doi:10.22605/rrh2561 · Cited by 37 · see citing works
Muders, P., Zahrt-Omar, C. A., Bussmann, S., Haberstroh, J., & Weber, M. (2014) · Palliative & Supportive Care · doi:10.1017/s1478951513001107 · Cited by 35 · see citing works
Towards better support for family carers: A richer understanding
Payne, S. A., & Grande, G. (2013) · Palliative Medicine · doi:10.1177/0269216313488856 · Cited by 26 · see citing works
Determinants of a hopeful attitude among family caregivers in a palliative care setting
Kim, S.-Y., Kim, J., Kim, S., Kang, H., Shin, I., Shim, H., Cho, S., Chung, I., & Yoon, J. (2013) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2013.10.020 · Cited by 26 · see citing works
Hasson‐Ohayon, I., Goldzweig, G., Sela-Oren, T., Pizem, N., Bar‐Sela, G., & Wolf, I. (2013) · Palliative & Supportive Care · doi:10.1017/s1478951513000242 · Cited by 26 · see citing works
Tokem, Y., Özçelik, H., & Cicik, A. (2014) · Cancer Nursing · doi:10.1097/ncc.0000000000000189 · Cited by 26 · see citing works
Describing and understanding depression in spouses of cancer patients in palliative phase
Fasse, L., Flahault, C., Brédart, A., Dolbeault, S., & Sultan, S. (2015) · Psycho-Oncology · doi:10.1002/pon.3777 · Cited by 25 · see citing works
The new EPS: Epidemiology and Psychiatric Sciences
Tansella, M. (2011) · Epidemiology and Psychiatric Sciences · doi:10.1017/s2045796011000035 · Cited by 20 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
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Liu, Z., Heffernan, C., & Tan, J. (2020) · International Journal of Nursing Sciences · doi:10.1016/j.ijnss.2020.07.012 · Cited by 749 · see citing works
Yu, W., Chen, J., Sun, S., Liu, P., Ouyang, L., & Hu, J. (2021) · Psycho-Oncology · doi:10.1002/pon.5667 · Cited by 40 · see citing works
Hu, H., Hu, X., & Xu, Y. (2023) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1194774 · Cited by 35 · see citing works
Spatuzzi, R., Giulietti, M. V., Ricciuti, M., Merico, F., Romito, F., Reggiardo, G., Birgolotti, L., Fabbietti, P., Raucci, L., Rosati, G., et al. (2020) · American Journal of Hospice and Palliative Medicine® · doi:10.1177/1049909119890840 · Cited by 34 · see citing works
Oleas Rodríguez, D., Yong Peña, C., Garza Olivares, X., Teixeira Filho, F., Lucero Córdova, J., & Salas Naranjo, A. (2024) · Psychology Research and Behavior Management · doi:10.2147/prbm.s443200 · Cited by 13 · see citing works
Lenzo, V., Sardella, A., Musetti, A., Petralia, M. C., Grado, I., & Quattropani, M. C. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph191911930 · Cited by 10 · see citing works
Psychological predictors of quality of life among Jordanian cancer patients' caregivers
Alnajar, M., Mosleh, S., Almalik, M., & Darawad, M. (2022) · Psycho-Oncology · doi:10.1002/pon.6054 · Cited by 7 · see citing works
Exploring the Unmet Needs of Cancer Caregivers in India: A Cross-Sectional Survey
Muralidharan, S., Sikalgar, F. R., B, D., Nikalje, M. R., Subramaniam, T., & Kumar, M. (2024) · Cureus · doi:10.7759/cureus.62159 · Cited by 3 · see citing works
“A high number of unmet needs correlate with psychological distress and overall caregiver burden [4].”
Background
- Authors
- Schrank, B., Ebert‐Vogel, A., Amering, M., Masel, E. K., Neubauer, M., Watzke, H., Zehetmayer, S., & Schur, S.
- Affiliations
- Medical University of Vienna (AT)
- Corresponding author
- Schur, Sophie
- Venue
- Psycho-Oncology
- Publisher
- Wiley
- Published
- 2015-10-18
- Volume
- 25
- Issue
- 7
- Pages
- 808-814
- ISSN
- 1057-9249 (ISSN-L)
- 1099-1611
- OpenAlex
- W1941372448
- Cited by
- 143
- References
- 42
- Citations by year
- 2026: 10 · 2025: 9 · 2024: 20 · 2023: 14 · 2022: 14 · 2021: 15 · 2020: 24 · 2019: 14 · 2018: 8 · 2017: 9 · 2016: 5
- FWCI
- 7.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Psycho-Oncology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative Care and End-of-Life Issues
- Health Sciences › Health Professions › Pharmacy › Nursing care and research
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative and Oncologic Care
- Keywords
- caregiver burden, gender differences, family caregivers, terminal cancer patients, advanced cancer, hope, coping styles, emotion-focused coping, support needs, psychological support interventions, palliative care, informal care
- MeSH terms
- Adaptation, Psychological, Adult, Aged, Family, Family Health, Female, Humans, Male, Middle Aged, Neoplasms, Surveys and Questionnaires, Sex Factors, Caregivers, Terminally Ill
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