Abstract
Introduction
Getting cancer is stressful for most patients and their relatives, and research has shown that psychosocial support is needed. Still, cancer care fails to appropriately address psychosocial problems associated with cancer. Research on this topic is often seen from the perspective of either the patient or the relative, even though it is suggested that psychosocial support is beneficial for the patient and the relative as a pair. Furthermore, research on the need for psychosocial support rarely involves patients with gynecological and lung cancer and their relatives, even though they often suffer from isolation and stigmatization. The aim of this review was therefore to summarize knowledge about psychosocial support with regard to individual needs, involvement of significant others, and providers of psychosocial support focusing on this specific population.
Method
A narrative review procedure was chosen. This method is a specific kind of review, which summarizes, explains, and interprets evidence on a selected topic. The review process was structured according to typical scholarly articles with attention to the search and review process.
Results
A total of 16 studies were included in the review. The studies were divided into two main categories: (1) studies focusing on needs for psychosocial support; and (2) studies focusing on interventions. The needs studies were analyzed, and three themes emerged: the needs of the patient and the significant other across the cancer trajectory; the needs of the significant other as a carer; and needs and ongoing and tailored support. The intervention studies were directed toward the patient and the relative, the patient, or the relative. Five interventions comprising various forms of support that were purely supportive and were carried out by healthcare professionals were identified.
Conclusion
There were overlaps between the needs of the patient and the relative, but there were also distinctive characteristics of the needs in the two groups. The needs varied during the cancer trajectory, and we therefore recommend that support be offered continuously. It was also evident that the relatives should be involved in the patients’ care and that the involvement was beneficial for both the patient and the relative.
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References
Galway K, Black A, Cantwell M, Cardwell CR, Mills M, Donnelly M. Psychosocial interventions to improve quality of life and emotional wellbeing for recently diagnosed cancer patients. Cochrane Database Syst Rev. 2012;11:CD007064.
Seibaek L, Petersen LK, Blaakaer J, Hounsgaard L. Hoping for the best, preparing for the worst: the lived experiences of women undergoing ovarian cancer surgery. Eur J Cancer Care (Engl). 2012;21(3):360–71.
Johnson RL, Gold MA, Wyche KF. Distress in women with gynecologic cancer. Psychooncology. 2010;19(6):665–8.
Ka’opua LS, Gotay CC, Boehm PS. Spiritually based resources in adaptation to long-term prostate cancer survival: perspectives of elderly wives. Health Soc Work. 2007;32(1):29–39.
Scott JL, Halford WK, Ward BG. United we stand? The effects of a couple–coping intervention on adjustment to early stage breast or gynecological cancer. J Consult Clin Psychol. 2004;72(6):1122–35.
Adler NE, Page AEK. Cancer care for the whole patient: meeting psychosocial health needs. Washington: National Academies; 2008.
Dalton SO, Bidstrup PE, Johansen C. Rehabilitation of cancer patients: needed, but how? Acta Oncol. 2011;50(2):163–6.
Thorsen L, Gjerset GM, Loge JH, Kiserud CE, Skovlund E, Flotten T, et al. Cancer patients’ needs for rehabilitation services. Acta Oncol. 2011;50(2):212–22.
Ernstmann N, Neumann M, Ommen O, Galushko M, Wirtz M, Voltz R, et al. Determinants and implications of cancer patients’ psychosocial needs. Support Care Cancer. 2009;17(11):1417–23.
Angen MJ, Simpson JS, Macrae H, Hundleby M. Impact of a residential psychosocial program for cancer patients: a focus group investigation. Adv Mind Body Med. 2003;19(3–4):24–34.
Eriksson E, Lauri S. Informational and emotional support for cancer patients’ relatives. Eur J Cancer Care (Engl). 2000;9(1):8–15.
Given BA, Northouse L. Who cares for family caregivers of patients with cancer? Clin J Oncol Nurs. 2011;15(5):451–2.
Ellis J, Wagland R, Tishelman C, Williams ML, Bailey CD, Haines J, et al. Considerations in developing and delivering a nonpharmacological intervention for symptom management in lung cancer: the views of patients and informal caregivers. J Pain Symptom Manage. 2012;44(6):831–42.
Sutton LB, Erlen JA. Effects of mutual dyad support on quality of life in women with breast cancer. Cancer Nurs. 2006;29(6):488–98.
McLean LM, Jones JM, Rydall AC, Walsh A, Esplen MJ, Zimmermann C, et al. A couples intervention for patients facing advanced cancer and their spouse caregivers: outcomes of a pilot study. Psychooncology. 2008;17(11):1152–6.
Morgan MA, Small BJ, Donovan KA, Overcash J, McMillan S. Cancer patients with pain the spouse/partner relationship and quality of life. Cancer Nurs. 2011;34(1):13–23.
Chambers SK, Pinnock C, Lepore SJ, Hughes S, O’Connell DL. A systematic review of psychosocial interventions for men with prostate cancer and their partners. Patient Educ Couns. 2011;85(2):e75–88.
Hagedoorn M, Dagan M, Puterman E, Hoff C, Meijerink WJ, DeLongis A, et al. Relationship satisfaction in couples confronted with colorectal cancer: the interplay of past and current spousal support. J Behav Med. 2011;34(4):288–97.
La Cour K, Ledderer L, Hansen HP. “An arena for sharing”: exploring the joint involvement of patients and their relatives in a cancer rehabilitation study. Cancer Nurs. doi:10.1097/NCC.0000000000000149. (Epub 2014 May 14 [cited 2014 June 6]).
Ledderer L, La Cour K, Mogensen O, Jakobsen E, Depont CR, Kragstrup J, et al. Feasibility of a psychosocial rehabilitation intervention to enhance the involvement of relatives in cancer rehabilitation: pilot study for a randomized controlled trial. Patient. 2013;6(3):201–12.
Ledderer L, La Cour K, Hansen HP. Outcome of supportive talks in a hospital setting: insights from cancer patients and their relatives. Patient. 2014;7(2):219–29.
Sandelowski M, Barroso J. Handbook for synthesizing qualitative research. New York: Springer; 2007.
Noblit GW, Hare RD. Meta-ethnography: synthesizing qualitative studies. Newbury Park: Sage; 1988.
Mays N, Pope C, Popay J. Systematically reviewing qualitative and quantitative evidence to inform management and policy-making in the health field. J Health Serv Res Policy. 2005;10(Suppl 1):6–20.
Haneline M. Understanding literature review designs. J Am Chiropr Assoc. 2007; 19–23.
Dixon-Woods M, Agarwal S, Jones DR, Young B, Sutton AJ. Synthesising qualitative and quantitative evidence: a review of possible methods. J Health Serv Res Policy. 2005;10(1):45–53.
Cooper HM. Research synthesis and meta-analysis. 4th ed. Los Angeles: Sage; 2010.
Paterson BL, Thorne S, Canam C, Jillings C. Meta-study of qualitative health research. Thousand Oaks: Sage; 2001.
Jones ML. Application of systematic review methods to qualitative research: practical issues. J Adv Nurs. 2004;48(3):271–8.
Mays N, Pope C. Qualitative research in health care: assessing quality in qualitative research. Br Med J. 2000;320(7226):50–2.
Walsh D, Downe S. Appraising the quality of qualitative research. Midwifery. 2006;22:108–19.
Rolfe G. Validity, trustworthiness and rigour: quality and the idea of qualitative research. J Adv Nurs. 2006;53(3):304–10.
Dixon-Woods M, Booth A, Sutton AJ. Synthesizing qualitative research: a review of published reports. Qual Res. 2007;7(3):375–422.
Dixon-Woods M, Sutton A, Shaw R, Miller T, Smith J, Young B, et al. Appraising qualitative research for inclusion in systematic reviews: a quantitative and qualitative comparison of three methods. J Health Serv Res Policy. 2007;12(1):42–7.
Hansen HP, Lee A, van Randwijk CB. Patient aspects: a review of fifty-eight Danish HTA reports. Int J Technol Assess Health Care. 2011;27(4):330–6.
Hoeck B. A clinically oriented and practice driven approach to metasynthesis: a worked example on “being critically ill in an ICU”. Aarhus: University of Aarhus; 2011.
Hansen HP, Draborg E, Kristensen FB. Exploring qualitative research synthesis: the role of patients’ perspectives in health policy design and decision making. Patient. 2011;4(3):143–52.
Evans D. Systematic reviews of interpretive research: interpretive data synthesis of processed data. Aust J Adv Nurs. 2002;20(2):22–6.
Sandelowski M. Whatever happened to qualitative description? Res Nurs Health. 2000;23:334–40.
Akyuz A, Guvenc G, Ustunsoz A, Kaya T. Living with gynecologic cancer: experience of women and their partners. J Nurs Scholarsh. 2008;40(3):241–7.
Badr H, Taylor CL. Social constraints and spousal communication in lung cancer. Psychooncology. 2006;15(8):673–83.
Hodgkinson K, Butow P, Hobbs KM, Wain G. After cancer: the unmet supportive care needs of survivors and their partners. J Psychosoc Oncol. 2007;25(4):89–104.
Illingworth N, Forbat L, Hubbard G, Kearney N. The importance of relationships in the experience of cancer: a re-working of the policy ideal of the whole-systems approach. Eur J Oncol Nurs. 2010;14(1):23–8.
Krishnasamy M, Wells M, Wilkie E. Patients and carer experiences of care provision after a diagnosis of lung cancer in Scotland. Support Care Cancer. 2007;15(3):327–32.
Griffiths J, Willard C, Burgess A, Amir Z, Luker K. Meeting the ongoing needs of survivors of rarer cancer. Eur J Oncol Nurs. 2007;11(5):434–41.
Mikkelsen TH, Sondergaard J, Jensen AB, Olesen F. Cancer rehabilitation: psychosocial rehabilitation needs after discharge from hospital? Scan J Prim Health Care. 2008;26(4):216–21.
Koldjeski D, Kirkpatrick MK, Everett L, Brown S, Swanson M. The ovarian cancer journey of families the first postdiagnostic year. Cancer Nurs. 2007;30(3):232–42.
Carlsson ME, Strang PM. Educational support programme for gynaecological cancer patients and their families. Acta Oncol. 1998;37(3):269–75.
Cox A, Bull E, Cockle-Hearne J, Knibb W, Potter C, Faithfull S. Nurse led telephone follow up in ovarian cancer: a psychosocial perspective. Eur J Oncol Nurs. 2008;12(5):412–7.
Pistrang N, Jay Z, Gessler S, Barker C. Telephone peer support for women with gynaecological cancer: recipients’ perspectives. Psychooncology. 2012;21(10):1082–90.
Walker LM, Bischoff TF, Robinson JW. Supportive expressive group therapy for women with advanced ovarian cancer. Int J Group Psychother. 2010;60(3):407–27.
Sekse RJ, Blaaka G, Buestad I, Tengesdal E, Paulsen A, Vika M. Education and counselling group intervention for women treated for gynaecological cancer: does it help? Scand J Caring Sci. 2014;28(1):112–21.
Nissim R, Freeman E, Lo C, Zimmermann C, Gagliese L, Rydall A, et al. Managing Cancer and Living Meaningfully (CALM): a qualitative study of a brief individual psychotherapy for individuals with advanced cancer. Palliat Med. 2012;26(5):713–21.
Richardson A, Plant H, Moore S, Medina J, Cornwall A, Ream E. Developing supportive care for family members of people with lung cancer: a feasibility study. Supportive Care Cancer. 2007;15(11):1259–69.
Ryan PJ, Howell V, Jones J, Hardy EJ. Lung cancer, caring for the caregivers: a qualitative study of providing pro-active social support targeted to the carers of patients with lung cancer. Palliat Med. 2008;22(3):233–8.
Source of Funding
This study was funded by the Danish Cancer Society (grant number OKV 08008).
Author contributions
Bente Hoeck was primarily responsible for the manuscript preparation, with contributions from Loni Ledderer and Helle Ploug Hansen. All authors were involved in critically revising the manuscript, and all authors have read and approved the final manuscript.
Contributors
Jakob Kragstrup, Ole Mogensen, Erik Jakobsen, and Helle Ploug Hansen conceived the study and developed the design of the overall study. Loni Ledderer led the project.
Conflicts of interest
The authors declare no conflict of interest, and the authors alone are responsible for the content of the paper.
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Hoeck, B., Ledderer, L. & Hansen, H.P. Involvement of Patients with Lung and Gynecological Cancer and Their Relatives in Psychosocial Cancer Rehabilitation: A Narrative Review. Patient 8, 127–143 (2015). https://doi.org/10.1007/s40271-014-0076-x
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DOI: https://doi.org/10.1007/s40271-014-0076-x