Informal caregiving in head and neck cancer: caregiving activities and psychological well-being
Open accessAbstract
The purpose of this study was to quantify the general cancer support activities that long-term carers of head and neck cancer (HNC) survivors engage in; and the relationships between these care activities and psychological well-being. Respondents answered a survey detailing their caring activities, the amount of time that they spent on those activities and how comfortable they felt engaging in them. Psychological well-being was assessed by the Depression Anxiety Stress Scales-21. A total of 197 carers took part in the study. The majority (76%) were women, mean age 57.4. Mean time since diagnosis was 6.2 years. In the past month, 45% of carers did not spend any extra time per week helping their relative/friend with general caring activities such as cleaning the house; 31% spent 1-19 hr/week and 23% spent 20 or more hours/week doing so. Most carers were comfortable assisting their relative/friend, though more carers felt uncomfortable assisting with HNC-specific support tasks (31% uncomfortable helping with medication) compared with general support tasks (7% uncomfortable helping with appointments). Feeling uncomfortable with head and neck-specific care tasks was a significant predictor of experiencing depression and anxiety.
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In one study on head and neck cancer, informal caregivers felt greater distress when assisting with caregiving tasks related to cancer-specific care than those related to general supportive care.
“In one study on head and neck cancer, informal caregivers felt greater distress when assisting with caregiving tasks related to cancer-specific care (e.g. helping with medications) than those related to general supportive care (e.g. coordinating appointments) [39].”
From Systematic review of caregiver burden, unmet needs and quality-of-life among informal caregivers of patients with pancreatic cancer (2023) · cites this paper as [39]
Feeling uncomfortable with cancer-specific care was predictive of informal caregivers' anxiety and depression.
“Feeling uncomfortable with cancer-specific care was predictive of informal caregivers’ anxiety and depression [39].”
From Systematic review of caregiver burden, unmet needs and quality-of-life among informal caregivers of patients with pancreatic cancer (2023) · cites this paper as [39]
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Cites
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
Vickery, L. E., Latchford, G., Hewison, J., Bellew, M., & Feber, T. (2003) · Head & Neck · doi:10.1002/hed.10206 · Cited by 201 · see citing works
Distress in Spouses and Patients After Treatment for Head and Neck Cancer
Verdonck‐de Leeuw, I. M., Eerenstein, S. E., Van der Linden, M. H., Kuik, D. J., de Bree, R., & Leemans, C. R. (2007) · The Laryngoscope · doi:10.1097/01.mlg.0000250169.10241.58 · Cited by 160 · see citing works
Lambert, S. D., Girgis, A., Lecathelinais, C., & Stacey, F. (2013) · Supportive Care in Cancer · doi:10.1007/s00520-012-1495-7 · Cited by 135 · see citing works
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Research works printed but not linked: 13
- Blood, G., Simpson, K., Dineen, M., Kauffman, S., & Raimondi, S. (1994). Spouses of individuals with laryngeal cancer: Caregiver strain and bur- den. Journal of Communication Disorders, 27, 19-35.
- Bookman, A., & Harrington, M. (2007). Family caregivers: A shadowy work- force in the Geriatric health care system. Journal of Health Politics Policy Law, 32, 1005-1041.
- Dempster, M., McCorry, N., Brennan, E., Donnelly, M., Murray, L., & John- ston, B. (2011). Illness perceptions among carer-survivor dyads related to psychological distress among Oesophageal cancer survivors. Journal of Psychosomatic Research, 70, 432-439.
- Girgis, A., Lambert, S., Johnson, C., Waller, A., & Currow, D. (2013). Physical, psychosocial, relationship and economic burden of caring for people with cancer: A review. Journal of Oncology Practice, 9, 197-202.
- Given, B., Given, C., & Kozachik, S. (2001). Family support in advanced can- cer. Canadian Journal of Clinical Cancer, 51, 213-231.
- Henry, J., & Crawford, J. (2005). The short-form version of the Depression Anxiety Stress Scales (DASS-21): Construct validity and normative data in a large non-clinical sample. British Journal of Clinical Psychology, 44, 227-239.
- Lee, Y., Lin, P., Chieln, C., & Fang, F. (2014). Prevalence and risk factors of depressive disorder in caregivers of patients with head and neck can- cer. Psychooncology, 24, 155-161. doi: 10.1002/pon.3619 · DOI
- Maddems, J., Utley, M., & Moller, H. (2012). Projections of cancer preva- lence in the United Kingdom, 2010-2040. British Journal of Cancer, 107, 1195-1202.
- Mehanna, H., Paleri, V., West, C., & Nutting, C. (2010). Head and neck can- cer: Epidemiology, presentation and prevention. British Medical Journal, 341, 663-666.
- Mehta, A., Chan, L., & Cohen, S. (2014). Flying blind: Sources of distress for family caregivers of palliative cancer patients managing cancer at home. Journal of Psychosocial Oncology, 32, 94-111.
- Olson, R. (2014). A time-sovereignty approach to understanding carers of cancer patients' experiences and support preferences. European Journal of Cancer Care, 23, 239-248.
- Pearce, A., Timmons, A., O' Sullivan, E., Gallagher, P., Gooberman-Hill, R., Thomas, A., … & Sharp, L. (2014). Long-term workforce participation patterns following head and neck cancer. Journal of Cancer Survivorship, 9, 30-39.
- Precious, E., Haran, S., Lowe, D., & Rogers, S. (2012). Head and neck cancer patients' perspectives of carer burden. British Journal of Oral and Maxil- lofacial Surgery, 50, 202-207.
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Informal caregiver burden for solid tumour cancer patients: a review and future directions
Thana, K., Lehto, R., Sikorskii, A., & Wyatt, G. (2021) · Psychology & Health · doi:10.1080/08870446.2020.1867136 · Cited by 97 · see citing works
Chong, E., Crowe, L., Mentor, K., Pandanaboyana, S., & Sharp, L. (2023) · Supportive Care in Cancer · doi:10.1007/s00520-022-07468-7 · Cited by 86 · see citing works
“Feeling uncomfortable with cancer-specific care was predictive of informal caregivers’ anxiety and depression [39].”
Self-citation
- Authors
- Balfe, M., O'Brien, K. M., Timmons, A., Butow, P., O'Sullivan, E., Gooberman-Hill, R., & Sharp, L.
- Affiliations
- National Cancer Registry (IE)
- The University of Sydney (AU)
- School of Dentistry; University College Cork; Cork Ireland
- Musculskeletal Research Unit; University of Bristol; Bristol UK
- Corresponding author
- Balfe, M.
- Venue
- European Journal of Cancer Care
- Publisher
- Wiley
- Published
- 2016-06-07
- Volume
- 27
- Issue
- 2
- Pages
- e12520
- ISSN
- 0961-5423 (ISSN-L)
- OpenAlex
- W2415359284
- Cited by
- 25
- References
- 4
- Citations by year
- 2026: 1 · 2024: 1 · 2023: 4 · 2022: 4 · 2021: 5 · 2020: 2 · 2019: 2 · 2018: 4 · 2017: 1 · 2016: 1
- FWCI
- 6.12
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- European Journal of Cancer Care (publishedVersion)
- PubMed (publishedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- Health Research Board
- Topics
- Health Sciences › Health Professions › Pharmacy › Nursing care and research
- Health Sciences › Medicine › Oncology › Cancer survivorship and care
- Health Sciences › Medicine › Otorhinolaryngology › Head and Neck Cancer Studies
- Keywords
- informal care, head and neck cancer, cancer survivors, psychological well-being, depression, anxiety, caregiver burden, caregiver comfort, medication support, caregiver time
- MeSH terms
- Adult, Aged, Anxiety, Depressive Disorder, Female, Head and Neck Neoplasms, Humans, Male, Middle Aged, Risk Factors, Social Support, Stress, Psychological, Logistic Models, Caregivers, Self Efficacy
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