Seeking, accepting and declining help for emotional distress in cancer: A systematic review and thematic synthesis of qualitative evidence
Corresponding Author
C.M. Carolan MB ChB, MRCP, MRCGP, MSc
Lecturer, Sessional GP, GP Appraiser, Appraisal Lead (Primary Care)
Faculty of Health Sciences and Sport, University of Stirling (Western Isles Campus), Stornoway, UK
NHS Western Isles, Stornoway, UK
Correspondence
Clare M. Carolan, Faculty of Health Sciences and Sport, University of Stirling, Western Isles Hospital, Stornoway, UK.
Email: [email protected]
Search for more papers by this authorA. Smith RN, RNT, BA, MA, PhD
Senior Lecturer/Head Life Sciences
Faculty of Health Sciences and Sport, University of Stirling (Western Isles Campus), Stornoway, UK
Search for more papers by this authorG.R. Davies BSc, PG Cert, MSc, FHEA, PhD, CPsychol
Lecturer and Scheme Co-Ordinator, UHI Honorary Research Fellow
PGT Tertiary & Higher Education, Faculty of Arts, Humanities and Business, Lews Castle College UHI, Stornoway, UK
Search for more papers by this authorL. Forbat BA, PG Cert, MSc, PhD
Professor
Palliative Care, Australian Catholic University and Calvary Health Care, Australian Catholic University, Canberra, ACT, Australia
Search for more papers by this authorCorresponding Author
C.M. Carolan MB ChB, MRCP, MRCGP, MSc
Lecturer, Sessional GP, GP Appraiser, Appraisal Lead (Primary Care)
Faculty of Health Sciences and Sport, University of Stirling (Western Isles Campus), Stornoway, UK
NHS Western Isles, Stornoway, UK
Correspondence
Clare M. Carolan, Faculty of Health Sciences and Sport, University of Stirling, Western Isles Hospital, Stornoway, UK.
Email: [email protected]
Search for more papers by this authorA. Smith RN, RNT, BA, MA, PhD
Senior Lecturer/Head Life Sciences
Faculty of Health Sciences and Sport, University of Stirling (Western Isles Campus), Stornoway, UK
Search for more papers by this authorG.R. Davies BSc, PG Cert, MSc, FHEA, PhD, CPsychol
Lecturer and Scheme Co-Ordinator, UHI Honorary Research Fellow
PGT Tertiary & Higher Education, Faculty of Arts, Humanities and Business, Lews Castle College UHI, Stornoway, UK
Search for more papers by this authorL. Forbat BA, PG Cert, MSc, PhD
Professor
Palliative Care, Australian Catholic University and Calvary Health Care, Australian Catholic University, Canberra, ACT, Australia
Search for more papers by this authorAbstract
Many individuals affected by cancer who experience emotional distress report not wanting help. This review aims to understand why individuals affected by cancer seek, accept or decline help for emotional distress and what influences these actions. A systematic review and thematic synthesis of the qualitative literature was conducted. Using pre-defined search terms, four electronic databases were searched from January 2000 to May 2016. Pre-determined inclusion and exclusion criteria were then applied. Identified papers were quality appraised. In total, 32 papers were included in the synthesis. Four themes emerged from data synthesis: attaining normality—the normality paradox; being emotionally literate; perceptions of help; needs-support gap. Attaining normality is ideographic, context dependent and temporally situated; some individuals maintain normality by not seeking/declining help whereas others seek/accept help to achieve a new normality. Thus, attaining normality paradoxically functions to explain both why individuals sought/accepted help or did not seek/declined help. Data indicate that a context dependent, systems thinking approach is merited to enhance psychosocial care. In particular, clinicians must actively explore the personal context of an individual's distress to ensure that help desired and help offered are mutually understood. Further research must address the limitations of the current evidence base to advance theoretical understanding.
REFERENCES
- Adams, R. N., Winger, J. G., & Mosher, C. E. (2015). A meta-analysis of the relationship between social constraints and distress in cancer patients. Journal of Behavioural Medicine, 38, 294–305.
- Andersen, R. M. (1995). Revisiting the behavioral model and access to medical care: Does it matter? Journal of Health & Social Behavior, 36, 1–10.
- Azuero, C., Allen, R., Kvale, E., Azuero, A., & Parmelee, P. (2014). Determinants of psychology service utilization in a palliative care outpatient population. Psycho-Oncology, 23(6), 650–657.
- Baker, P., Beesley, H., Dinwoodie, R., Fletcher, I., Ablett, J., Holcombe, C., & Salmon, P. (2013). ‘You're putting thoughts into my head’: A qualitative study of the readiness of patients with breast, lung or prostate cancer to address emotional needs through the first 18 months after diagnosis. Psycho-Oncology, 22(6), 1402–1410.
- Baker, P., Beesley, H., Fletcher, I., Ablett, J., Holcombe, C., & Salmon, P. (2016). ‘Getting back to normal’ or ‘a new type of normal’? A qualitative study of patients’ responses to the existential threat of cancer. European Journal of Cancer Care, 25, 180–189.
- Baker-Glenn, E. A., Park, B., Granger, L., Symonds, P., & Mitchell, A. J. (2010). Desire for psychological support in cancer patients with depression or distress: Validation of a simple help question. Psycho-Oncology, 20(5), 525–531.
- Barnett-Page, E., & Thomas, J. (2009) Methods for the synthesis of qualitative research: A critical review. NCRM Working Paper. NCRM. Retrieved from http://eprints.ncrm.ac.uk/690/1/0109%2520Qualitative%2520synthesis%2520methods%2520paper%2520NCRM.pdf (accessed 17 February 2017).
- Beaver, K., Williamson, S., & Briggs, J. (2016). Exploring patient experiences of neo-adjuvant chemotherapy for breast cancer. European Journal of Oncology Nursing, 20, 77–86.
- Biddle, L, Donovan, J, Sharp, D., & Gunnell, D. (2007) Explaining non-help-seeking amongst young adults with mental distress: A dynamic interpretive model of illness behaviour. Sociology of Health & Illness, 29, 983–1002.
- Bird, J., Coleman, P., & Danson, S. (2015). Coping with melanoma-related worry: A qualitative study of the experiences and support needs of patients with malignant melanoma. Journal of Clinical Nursing, 24(7/8), 937–947.
- Bjelland, I., Dahl, A. A., Haug, T. T., & Neckelmann, D. (2002). The validity of the Hospital Anxiety and Depression Scale: An updated literature review. Journal of Psychosomatic Research, 52, 69–77.
- Braamse, A. M., vanMeijel, B., Visser, O. J., Huijgens, P. C., Beekman, A. T., & Dekker, J. (2016). Help-seeking behaviour of patients with haematological malignancies treated with autologous stem cell transplantation. European Journal of Cancer Care. https://doi.org/10.1111/ecc.12454 [Epub ahead of print].
- Bray, F., Ren, J. S., Eric Masuyer, E., & Ferlay, J. (2013). Global estimates of cancer prevalence for 27 sites in the adult population in 2008. International Journal of Cancer, 132, 1133–1145.
- Brown, N. K., Lui, C., Robinson, P. C., & Boyle, F. M. (2015). Supportive care needs and preferences of lung cancer patients: A semi-structured qualitative interview study. Supportive Care in Cancer, 23(6), 1533–1539.
- Campbell, R., Pound, P., Morgan, M., Daker-White, G., Britten, N., Pill, R., … Donovan, J. (2011). Evaluating meta-ethnography: Systematic analysis and synthesis of qualitative research. Health Technology Assessment, 15(43), 1–164.
- Carlson, L. E., Angen, M., Cullum, J., Goodey, E., Koopmans, J., Lamont, L., … Bultz, B. D. (2004). High levels of untreated distress and fatigue in cancer patients. British Journal of Cancer, 90, 2297–2304.
- Carolan, C., Smith, A., & Forbat, L. (2015). Conceptualising psychological distress in families in palliative care: Findings from a systematic review. Palliative Medicine, 29(7), 605–632.
- Clarke, S., Booth, L., Velikova, G., & Hewison, J. (2006). Social support: Gender differences in cancer patients in the United Kingdom. Cancer Nursing, 29(1), 66–72.
- Clement, S., Schauman, O., Graham, T., Maggioni, F., Evans-Lacko, S., Bezborodovs, N., … Thornicroft, G. (2015). What is the impact of mental health-related stigma on help-seeking? A systematic review of quantitative and qualitative studies. Psychological Medicine, 45(1), 11–27.
- Clover, K., Kelly, P., Rogers, K., Britton, B., & Carter, G. (2013). Predictors of desire for help in oncology outpatients reporting pain or distress. Psycho-Oncology, 22(7), 1611–1617.
- Clover, K., Mitchell, A., Britton, B., & Carter, G. (2015). Why do oncology outpatients who report emotional distress decline help? Psycho-Oncology, 24(7), 812–818.
- Cooke, A., Smith, D., & Booth, A. (2012). Beyond PICO: The SPIDER Tool for Qualitative Evidence Synthesis. Qualitative Health Research, 22(10), 1435–1443.
- Corboy, D., McDonald, J., & McLaren, S. (2011). Barriers to accessing psychosocial support services among men with cancer living in rural Australia: Perceptions of men and health professionals. International Journal of Men's Health, 10(2), 163–183.
10.3149/jmh.1002.163 Google Scholar
- Corboy, D., McLaren, S., & McDonald, J. (2011). Predictors of support service use by rural and regional men with cancer. Australian Journal of Rural Health, 19(4), 185–190.
- Critical Appraisal Skills Programme (CASP). CASP checklists. Retrieved from http://media.wix.com/ugd/dded87_29c5b002d99342f788c6ac670e49f274.pdf (accessed 17 February 2017).
- Dilworth, S., Higgins, I., Parker, V., Kelly, B., & Turner, J. (2014). Patient and health professional's perceived barriers to the delivery of psychosocial care to adults with cancer: A systematic review. Psycho-Oncology, 23, 601–612.
- Dingwall, R. (2001). Aspects of illness ( 2nd edn). Farnham: Ashgate.
- Docherty, A. (2004). Experience, functions and benefits of a cancer support group. Patient Education and Counselling, 55(1), 87–93.
- Ekberg, K., McDermott, J., Little, P., Leydon, G., Moynihan, C., & Brindle, L. (2014). The role of helplines in cancer care: Intertwining emotional support with information or advice-seeking needs. Journal of Psychosocial Oncology, 32(3), 359–381.
- Ellis, J., Lin, J., Walsh, A., Lo, C., Shepherd, F. A., Moore, M., … Rodin, G. (2009). Predictors of referral for specialized psychosocial oncology care in patients with metastatic cancer: The contributions of age, distress, and marital status. Journal of Clinical Oncology, 27, 699–705.
- Ernstmann, N., Neumann, M., Ommen, O., Galushko, M., Wirtz, M., Voltz, R., … Pfaff, H. (2009). Determinants and implications of cancer patients’ psychosocial needs. Supportive Care in Cancer, 17(11), 1417–1423.
- Fennell, K. M., Turnbull, D. A., Bidargaddi, N., McWha, J. L., Davies, M., & Olver, I. (2016). The consumer-driven development and acceptability testing of a website designed to connect rural cancer patients and their families, carers and health professionals with appropriate information and psychosocial support. European Journal of Cancer Care. https://doi.org/10.1111/ecc.12533 [Epub ahead of print].
- Fuchsia Howard, A., Smillie, K., Ward, A., Kazanjian, A., Turnbull, K., Munroe, D., … Olson, R. (2014). Access to medical and supportive care for rural and remote cancer survivors in northern British Columbia. Journal of Rural Health, 30(3), 311–321.
- Gunn, K., Turnbull, D., McWha, J. L., Davies, M., & Olver, I. (2013). Psychosocial service use: A qualitative exploration from the perspective of rural Australian cancer patients. Supportive Care Cancer, 21(9), 2547–2555.
- Hagedoorn, M., Sanderman, R., Bolks, H. N., Tuinstra, J., & Coyne, J. C. (2008). Distress in couples coping with cancer: A meta-analysis and critical review of role and gender effects. Psychological Bulletin, 134, 1–30.
- Hagger, M. S., & Orbell, S. (2003). A meta-analytic review of the common-sense model of illness representations. Psychology & Health, 18(2), 141–184.
- Hansen, M. C., & Aranda, M. P. (2012). Sociocultural influences on mental health service use by Latino older adults for emotional distress: Exploring the mediating and moderating role of informal social support. Social Science in Medicine, 75(12), 2134–2142.
- Harley, C., Pini, S., Bartlett, Y. K., & Velikova, G. (2012). Defining chronic cancer: Patient experiences and self-management needs. BMJ Supportive and Palliative Care, 2(3), 248–255.
- Hill, H. C., Paley, J., & Forbat, L. (2014). Observations of professional-patient relationships: a mixed-methods study exploring whether familiarity is a condition for nurses’ provision of psychosocial support. Palliative Medicine, 28(3), 256–263.
- Hodges, L. J., Humphris, G. M., & Macfarlane, G. (2005). A meta-analytic investigation of the relationship between the psychological distress of cancer patients and their carers. Social Science in Medicine, 60, 1–12.
- Högberg, K., Sandman, L., Nyström, M., Broström, A., & Stockelberg, D. (2013). Prerequisites required for the provision and use of web-based communication for psychosocial support in haematologic care. European Journal of Oncology Nursing, 17(5), 596–602.
- Holland, J. C. (1999). Update: NCCN practice guidelines for the management of psychosocial distress. Oncology, 13, 459–507.
- Holland, J. C., Andersen, B., Breitbart, W. S., Buchmann, L. O., Compass, B., Deshields, T. L., … Freedman-Cass, D. A. (2013). NCCN Clinical Practice Guidelines in Oncology: Distress Management. Version 2, 2013. Available at: NCCN.org. Accessed April 22, 2014 cited in: Lambert, S.D., Kelly, B., Boyes, A., Cameron, A., Adams, C., Proietto, A. & Girgis, A. (2014). Insights into preferences for psycho-oncology services among women with gynecologic cancer following distress screening. Journal of the National Comprehensive Cancer Network, 12(6), 899–906.
- Hubbard, G., & Forbat, L. (2012). Cancer as biographical disruption: Constructions of living with cancer. Supportive Care in Cancer, 20, 2033–2040.
- Kadan-Lottick, N. S., Vanderwerker, L. C., Block, S. D., Zhang, B., & Prigerson, H. G. (2005). Psychiatric disorders and mental health service use in patients with advanced cancer. Cancer, 104, 2872–2881.
- Kanavaki, A. M., Rushton, A., Klocke, R., & Duda, J. L. (2016). Barriers and facilitators to physical activity in people with hip or knee osteoarthritis: Protocol for a systematic review of qualitative evidence. British Medical Journal Open, 6, e012049.
- Kessler, R. C., Aguilar-Gaxiola, S., Alonso, J., Chatterji, S., Lee, S., Ormel, J., … Wang, P. S. (2009). The global burden of mental disorders: An update from the WHO World Mental Health (WMH) Surveys. Epidemiologia E Psichiatria Sociale, 18(1), 23–33.
- Kobayakawa, M., Okamura, H., Yamagishi, A., Morita, T., Kawagoe, S., Shimizu, M., … Miyashita, M. (2016). Family caregivers require mental health specialists for end-of-life psychosocial problems at home: A nationwide survey in Japan. Psycho-Oncology, 25(6), 641–647.
- Lambert, S. D., Harrison, J. D., Smith, E., Bonevski, B., Carey, M., Lawsin, C., … Girgis, A. (2012). The unmet needs of partners and caregivers of adults diagnosed with cancer: A systematic review. BMJ Supportive and Palliative Care, 2(3), 224–230.
- Lambert, S. D., Kelly, B., Boyes, A., Cameron, A., Adams, C., Proietto, A., & Girgis, A. (2014). Insights into preferences for psycho-oncology services among women with gynecologic cancer following distress screening. Journal of the National Comprehensive Cancer Network, 12(6), 899–906.
- Lepore, S. J., & Revenson, T. A. (2007). Social constraints on disclosure and adjustment to cancer. Social and Personality Psychology Compass, 1, 313–333.
10.1111/j.1751-9004.2007.00013.x Google Scholar
- Letwin, S., Glenton, C., Munthe-Kaas, H., Carlsen, B., Colvin, C. J., Gülmezoglu, M., … Rashidian, A. (2015). Using qualitative evidence in decision making for health and social interventions: An approach to assess confidence in findings from qualitative evidence syntheses (GRADE-CERQual). PLoS Medicine, 12(10), 1–18.
- Leventhal, H., Meyer, D., & Nerenz, D. R. (1980). The common-sense model of illness danger. In S. Rachman (Ed.), Medical psychology, Vol. II. New York: Pergamon Press.
- Leventhal, H., Phillips, L. A., & Burns, E. (2016). The Common-Sense Model of Self-Regulation (CSM): A dynamic framework for understanding illness self-management. Journal Behavioural Medicine, 39, 935–946.
- Lloyd-Williams, M., Friedman, T., & Rudd, N. (2000). Criterion validation of the Edinburgh postnatal depression scale as a screening tool for depression in patients with advanced metastatic cancer. Journal of Pain and Symptom Management, 20, 259–265.
- Maguire, R., Forbat, L., Kearney, N., & Rowa-Dewar, N. (2009). ‘Quite an awkward situation to be in’: Perceptions of patients, carers and health and social care professionals of the supportive cancer care in British military personnel stationed in Germany. Supportive Care in Cancer, 17(10), 1269–1276.
- McDowell, M. E., Occhipinti, S., Ferguson, M., & Chambers, S. K. (2011). Prospective predictors of psychosocial support service use after cancer. Psycho-Oncology, 20, 788–791.
- McGrath, P. (2013). Receptivity: An important factor affecting supportive care provision. Journal Psychosocial Oncology, 31(1), 30–50.
- McGrath, P. (2014). Patient perspectives on the usefulness of routine telephone follow-up as psychosocial support for hematologic malignancies: Australian findings. Oncology Nursing Forum, 41(1), 40–44.
- Merckaert, I., Libert, Y., Lieutenant, F., Moucheux, A., Farvacques, C., Slachmuylder, J. L., & Razavi, D. (2013). Desire for formal psychological support among caregivers of patients with cancer: Prevalence and implications for screening their needs. Psycho-Oncology, 22(6), 1389–1395.
- Merckaert, I., Libert, Y., Messin, S., Milani, M., Slachmuylder, J. L., & Razavi, D. (2010). Cancer patients’ desire for psychological support: Prevalence and implications for screening patients’ psychological needs. Psycho-Oncology, 19(2), 141–149.
- Mitchell, A. (2013). Screening for cancer-related distress: When is implementation successful and when is it unsuccessful? Acta Oncologica, 52(2), 216–224.
- Mosher, C. E., Champion, V. L., Hanna, N., Jalal, S. I., Fakiris, A. J., Birdas, T. J., … Ostroff, J. S. (2013). Support service use and interest in support services among distressed family caregivers of lung cancer patients. Psycho-Oncology, 22, 1549–1556.
- Mosher, C. E., DuHamel, K. N., Rini, C. M., Li, Y., Isola, L., Labay, L., … Redd, W. H. (2010). Barriers to mental health service use among hematopoietic stem cell transplant survivors. Bone Marrow Transplantation, 45, 570–579.
- Mosher, C. E., Given, B. A., & Ostroff, J. S. (2015). Barriers to mental health service use among distressed family caregivers of lung cancer patients. European Journal of Cancer Care, 24(1), 50–59.
- Mosher, C. E., Hanna, N., Jalal, S. I., Fakiris, A. J., Einhorn, L. H., Birdas, T. J., … Champion, V. L. (2013). Support service use and interest in support services among lung cancer patients. Lung Cancer, 82, 162–167.
- Mosher, C., Winger, J., Hanna, N., Jalal, S., Fakiris, A., Einhorn, L. H., … Champion, V. L. (2014). Barriers to mental health service use and preferences for addressing emotional concerns among lung cancer patients. Psycho-Oncology, 23(7), 812–819.
- Neumann, M., Galushko, M., Karbach, U., Goldblatt, H., Visser, A., Wirtz, M., … Pfaff, H. (2010). Barriers to using psycho-oncology services: A qualitative research into the perspectives of users, their relatives, non-users, physicians, and nurses. Supportive Care in Cancer, 18(9), 1147–1156.
- Northouse, L. I., Katapodi, M. C., Schafenacker, A. M., & Weiss, D. (2012). The impact of caregiving on the psychological well-being of family caregivers and cancer patients. Seminars in Oncology Nursing, 28(4), 236–245.
- Olson, R. (2014). A time-sovereignty approach to understanding carers of cancer patients’ experiences and support preferences. European Journal of Cancer Care, 23(2), 239–248.
- Park, C., Shin, D. W., Choi, J. Y., Kang, J., Baek, Y. J., Mo, H. N., … Park, S. (2012). Determinants of the burden and positivity of family caregivers of terminally ill cancer patients in Korea. Psycho-Oncology, 21(3), 282–290.
- Pascal, J., Johnson, N., Dickson-Swift, V., Dangerfield, F., & McGrath, P. (2016). Understanding receptivity to informal supportive cancer care in regional and rural Australia: A Heideggerian analysis. European Journal of Cancer Care, 25(3), 381–390.
- Pascal, J., Johnson, N., Dickson-Swift, V., & Kenny, A. (2015). Returning home: Psychosocial care during the re-entry phase of cancer survivorship in rural Australia. European Journal of Cancer Care, 24(1), 39–49.
- Peters, D. H. (2014). The application of systems thinking in health: Why use systems thinking? Health Research Policy and Systems, 12, 51.
- Pitceathly, C., & Maguire, P. (2003). The psychological impact of cancer on patients’ partners and other key relatives: A review. European Journal of Cancer, 39(11), 1517–1524.
- Reeve, J., Lloyd-Williams, M., Payne, S., & Dowrick, C. (2009). Insights into the impact of clinical encounters gained from personal accounts of living with advanced cancer. Primary Health Care Research and Development, 10(4), 357–367.
10.1017/S1463423609001121 Google Scholar
- Regan, T., Lambert, S., Kelly, B., Falconier, M., Kissane, D., & Levesque, J. (2015). Couples coping with cancer: Exploration of theoretical frameworks from dyadic studies. Psycho-Oncology, 24(12), 1605–1617.
- Regan, T., Levesque, J., Lambert, S., & Kelly, B. (2015). A qualitative investigation of health care professionals’, patients’ and partners’ views on psychosocial issues and related interventions for couples coping with cancer. PLoS ONE, 10(7), e0133837.
- Rickwood, D., Thomas, K., & Bradford, S. (2012). Review of help-seeking measures in mental health: An Evidence Check rapid review brokered by the Sax Institute. Retrieved from https://www.saxinstitute.org.au/wp-content/uploads/02_Help-seeking-measures-in-mental-health.pdf (accessed February, 2017).
- Ring, N., Ritchie, K., Mandava, L., & Jepson, R. (2011). A guide to synthesising qualitative research for researchers undertaking health technology assessments and systematic reviews. Retrieved from http://www.healthcareimprovementscotland.org/our_work/technologies_and_medicines/programme_resources/synthesising_research.aspx (accessed 3 July 2016).
- Salmon, P., Clark, L., McGrath, E., & Fisher, P. (2015). Screening for psychological distress in cancer: Renewing the research agenda. Psycho-Oncology, 24(3), 262–268.
- Scholten, C., Weinländer, G., Krainer, M., Frischenschlager, O., & Zielinski, C. C. (2001). Difference in patient's acceptance of early versus late initiation of psychosocial support in breast cancer. Supportive Care in Cancer, 9, 459–464.
- Scott, S. E., Walter, F. M., Webster, A., Sutton, S., & Emery, J. (2013). The Model of Pathways to Treatment: Conceptualization and integration with existing theory. British Journal of Health Psychology, 18, 45–64.
- Shaw, J., Harrison, J., Young, J., Butow, P., Sandroussi, C., Martin, D., & Solomon, M. (2013). Coping with newly diagnosed upper gastrointestinal cancer: A longitudinal qualitative study of family caregivers’ role perception and supportive care needs. Supportive Care in Cancer, 21(3), 749–756.
- Shimizu, K., Akechi, T., Okamura, M., Oba, A., Fujimori, M., Akizuki, N., & Uchitomi, Y. (2005). Usefulness of the nurse-assisted screening and psychiatric referral program. Cancer, 103(9), 1949–1956.
- Sinfield, P., Baker, R., Ali, S., & Richardson, A. (2012). The needs of carers of men with prostate cancer and barriers and enablers to meeting them: A qualitative study in England. European Journal of Cancer Care, 21(4), 527–534.
- Skea, Z. C., MacLennan, S. J., Entwistle, V. A., & N'Dow, J. (2011). Patient perception, preference and participation: Enabling mutual helping? Examining variable needs for facilitated peer support. Patient Education and Counselling, 85(2), 120–125.
- Stajduhar, K. I., Thorne, S. E., McGuinness, L., & Kim-Sing, C. (2010). Patient perceptions of helpful communication in the context of advanced cancer. Journal of Clinical Nursing, 19(13–14), 2039–2047.
- Stamataki, Z., Brunton, L., Lorigan, P., Green, A., Newton-Bishop, J., & Molassiotis, A. (2015). Assessing the impact of diagnosis and the related supportive care needs in patients with cutaneous melanoma. Supportive Care in Cancer, 23, 779–789.
- Stapleton, S., & Pattison, N. (2015). The lived experience of men with advanced cancer in relation to their perceptions of masculinity: A qualitative phenomenological study. Journal of Clinical Nursing, 24(7/8), 1069–1078.
- Steele, R., & Fitch, M. I. (2008). Why patients with lung cancer do not want help with some needs. Supportive Care in Cancer, 16(3), 251–259.
- Steginga, S. K., Campbell, A., Ferguson, M., Beeden, A., Walls, M., Cairns, W., & Dunn, J. (2008). Socio-demographic, psychosocial and attitudinal predictors of help seeking after cancer diagnosis. Psycho-Oncology, 17(10), 997–1005.
- Tan, J., Butow, P., Boyle, F., Saw, R., & O'Reilly, A. (2014). A qualitative assessment of psychosocial impact, coping and adjustment in high-risk melanoma patients and caregivers. Melanoma Research, 24(3), 252–260.
- Thomas, J., & Harden, A. (2008). Methods for the thematic synthesis of qualitative research in systematic reviews. BMC Medical Research Methodology, 8, 45. https://doi.org/10.1186/1471-2288-8-45
- Thorne, S. E., Hislop, T. G., Stajduhar, K., & Oglov, V. (2009). Time-related communication skills from the cancer patient perspective. Psycho-Oncology, 18(5), 500–507.
- Tong, A., Sainsbury, P., & Craig, J. (2007). Consolidated criteria for reporting qualitative research (COREQ): A 32-item checklist for interviews and focus groups. International Journal of Qualitative Health Care, 19(6), 349–357.
- Traeger, L., Cannon, S., Keating, N., Pirl, W., Lathan, C., Martin, M. Y., … Park, E. (2014). Race by sex differences in depression symptoms and psychosocial service use among non-Hispanic black and white patients with lung cancer. Journal of Clinical Oncology, 32(2), 107–113.
- Tucker, J., Hammer, J., Vogel, D., Bitman, R., Wade, N., & Maier, E. (2013). Disentangling self-stigma: Are mental illness and help-seeking self-stigmas different? Journal of Counselling and Psychology, 60(4), 520–531.
- Tuinman, M. A., Gazendam-Donofrio, S. M., & Hoekstra-Weebers, J. E. (2008). Screening and referral for psychosocial distress in oncologic practice: Use of the Distress Thermometer. Cancer, 113, 870–878.
- Tuinman, M., Van Nuenen, F., Hagedoorn, M., & Hoekstra-Weebers, J. (2015). Distress, problems and referral wish of cancer patients: Differences according to relationship status and life phase. Psycho-Oncology, 24(6), 699–704.
- Vanderwerker, L. C., Laff, R. E., Kadan-Lottick, N. S., McColl, S., & Prigerson, H. G. (2005). Psychiatric disorders and mental health service use among caregivers of advanced cancer patients. Journal of Clinical Oncology, 23(28), 6899–6907.
- Van Scheppingen, C., Schroevers, M. J., Smink, A., van der Linden, Y. M., Mul, V. E., Langendijk, J. A., … Sanderman, R. (2011). Does screening for distress efficiently uncover meetable unmet needs in cancer patients? Psycho-Oncology, 20(6), 655–663.
- Walton, L., Reeve, J., Brown, P., & Farquhar, C. (2010). Gynaecologic cancer patients’ needs and experiences of supportive health services in New Zealand. Psycho-Oncology, 19(2), 201–208.
- Wenger, L., & Oliffe, J. (2014). Men managing cancer: A gender analysis. Sociology of Health & Illness, 36(1), 108–122.
- Wyke, S., Adamson, J., Dixon, D., & Hunt, K. (2013). Consultation and illness behaviour in response to symptoms: A comparison of models from different disciplinary frameworks and suggestions for future research directions. Social Science in Medicine, 86, 79–87.
- Zigmond, A. S., & Snaith, R. P. (1983). The hospital anxiety and depression scale. Acta Psychiatrica Scandinavica, 67, 361–370.
- Zola, I. K. (1973). Pathways to the doctor-from person to patient. Social Science & Medicine, 7, 677–689.