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Erschienen in: Supportive Care in Cancer 11/2007

01.11.2007 | Original Article

Developing supportive care for family members of people with lung cancer: a feasibility study

verfasst von: Alison Richardson, Hilary Plant, Sally Moore, Jibby Medina, Amanda Cornwall, Emma Ream

Erschienen in: Supportive Care in Cancer | Ausgabe 11/2007

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Abstract

Purpose

Families provide crucial support, yet their own needs often go unrecognised and, as a consequence, remain unmet. The purpose of this study was to evaluate a newly developed supportive intervention for family members of patients with lung cancer.

Materials and methods

A consecutive convenience sample of 25 family members of people with lung cancer received an individualised supportive intervention from a support nurse over a period of 12 weeks. This involved in-depth assessment followed up with a tailored plan of ongoing support to address informational, emotional, social and practical needs. A concurrent mixed method design explored perceptions and outcomes of those receiving the intervention and assess its appropriateness, acceptability and feasibility. Data were collected through a semi structured telephone interview with family members, and support nurses maintained a contact log. A questionnaire addressed emotional well-being [general health questionnaire (GHQ-12)], quality of life [quality of life family version (Family QoL)] and needs for care [family inventory of needs (FIN)]—at baseline and week 12.

Results

Family members perceived they had derived benefit from the intervention. Certain elements clearly emerged as important for participants, including being listened to by someone who could facilitate emotional expression, being provided with individually tailored information and receiving practical help and advice. Outcomes mapped to five main areas: information needs, communication between family members, emotional well-being, being supported and facilitating family member’s role. There was a trend for more needs to be met and quality of life and emotional well-being to improve at week 12.

Conclusion

This study has demonstrated that a supportive intervention for family members of patients with lung cancer can be delivered to good effect by experienced cancer nurses. The active components of the intervention have been distinguished and provide the basis for development of a larger sufficiently powered trial.
Literatur
1.
Zurück zum Zitat Thomas C, Morris SM, Harman JC (2002) Companions through cancer: the care given by informal carers in cancer contexts. Soc Sci Med 54(4):529–544PubMedCrossRef Thomas C, Morris SM, Harman JC (2002) Companions through cancer: the care given by informal carers in cancer contexts. Soc Sci Med 54(4):529–544PubMedCrossRef
2.
Zurück zum Zitat Plant H (2000) Living with cancer. Understanding the experiences of close relatives of people with cancer. PhD thesis. King’s College London Plant H (2000) Living with cancer. Understanding the experiences of close relatives of people with cancer. PhD thesis. King’s College London
3.
Zurück zum Zitat Krishnasamy M, Wilkie E (1999) Lung cancer: patients’, families’ and professionals’ perceptions of health care need. A national needs assessment study. Project Report. Practice Development Unit/Centre for Cancer and Palliative Care Studies, Macmillan, London Krishnasamy M, Wilkie E (1999) Lung cancer: patients’, families’ and professionals’ perceptions of health care need. A national needs assessment study. Project Report. Practice Development Unit/Centre for Cancer and Palliative Care Studies, Macmillan, London
4.
Zurück zum Zitat Department of Health (2000) The NHS cancer plan: a plan for investment. A plan for reform. HMSO, London Department of Health (2000) The NHS cancer plan: a plan for investment. A plan for reform. HMSO, London
5.
Zurück zum Zitat NICE (2004) Guidance on cancer services: improving supportive and palliative care for adults with cancer. The manual. National Institute for Clinical Excellence, London NICE (2004) Guidance on cancer services: improving supportive and palliative care for adults with cancer. The manual. National Institute for Clinical Excellence, London
6.
Zurück zum Zitat Harding R, Higginson IJ (2003) What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliat Med 17(1):63–74PubMedCrossRef Harding R, Higginson IJ (2003) What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliat Med 17(1):63–74PubMedCrossRef
7.
Zurück zum Zitat Clarke D (1993) Evaluating the needs of informal carers. Prog Palliat Care 1:3–5 Clarke D (1993) Evaluating the needs of informal carers. Prog Palliat Care 1:3–5
8.
Zurück zum Zitat James V (1998) Unwaged carers and the provision of health care. In: Field D, Taylor S (eds) Sociological perspectives on health, illness and health care. Blackwell, Oxford James V (1998) Unwaged carers and the provision of health care. In: Field D, Taylor S (eds) Sociological perspectives on health, illness and health care. Blackwell, Oxford
9.
Zurück zum Zitat Cribb A (2001) Knowledge and caring: a philosophical and personal perspective. In: Corner J, Bailey C (eds) Cancer nursing: care in context. Blackwell, Oxford Cribb A (2001) Knowledge and caring: a philosophical and personal perspective. In: Corner J, Bailey C (eds) Cancer nursing: care in context. Blackwell, Oxford
10.
Zurück zum Zitat Ferris F, Balfour H, Bowen K, Farley J, Hardwick M, Lamontagne C et al (2002) A model to guide hospice palliative care. Canadian Hospice Palliative Care Association, Ottowa, ON Ferris F, Balfour H, Bowen K, Farley J, Hardwick M, Lamontagne C et al (2002) A model to guide hospice palliative care. Canadian Hospice Palliative Care Association, Ottowa, ON
11.
Zurück zum Zitat Harding R, Higginson IJ, Leam C, Donaldson N, Pearce A, George R et al (2004) Evaluation of a short-term group intervention for informal carers of patients attending a home palliative care service. Journal of Pain and Symptom Management 27(5):396–408PubMedCrossRef Harding R, Higginson IJ, Leam C, Donaldson N, Pearce A, George R et al (2004) Evaluation of a short-term group intervention for informal carers of patients attending a home palliative care service. Journal of Pain and Symptom Management 27(5):396–408PubMedCrossRef
12.
Zurück zum Zitat Pitceathly C, Maguire P (2003) The psychological impact of cancer on patients’ partners and other key relatives: review. Eur J Cancer 39:1517–1524PubMedCrossRef Pitceathly C, Maguire P (2003) The psychological impact of cancer on patients’ partners and other key relatives: review. Eur J Cancer 39:1517–1524PubMedCrossRef
13.
Zurück zum Zitat Medical Research Council (2000) A framework for development and evaluation of RCTs for complex interventions to improve health. Medical Research Council, UK, (April 2000) Medical Research Council (2000) A framework for development and evaluation of RCTs for complex interventions to improve health. Medical Research Council, UK, (April 2000)
14.
Zurück zum Zitat Krishnasamy M, Wilkie E, Haviland J (2001) Lung cancer health care needs assessment: patients’ and informal carers’ response to a national mail questionnaire survey. Palliat Med 15:213–227PubMedCrossRef Krishnasamy M, Wilkie E, Haviland J (2001) Lung cancer health care needs assessment: patients’ and informal carers’ response to a national mail questionnaire survey. Palliat Med 15:213–227PubMedCrossRef
15.
Zurück zum Zitat Cancer Research UK (2005) Lung cancer: lung cancer survival statistics. Cancer Research UK, London Cancer Research UK (2005) Lung cancer: lung cancer survival statistics. Cancer Research UK, London
16.
Zurück zum Zitat Creswell JW (2003) Research design: qualitative, quantitative, and mixed methods approaches, 2nd edn. Sage, London Creswell JW (2003) Research design: qualitative, quantitative, and mixed methods approaches, 2nd edn. Sage, London
17.
Zurück zum Zitat Rogers C (1961) On becoming a person. Houghton Mifflin, Boston Rogers C (1961) On becoming a person. Houghton Mifflin, Boston
18.
Zurück zum Zitat McCormack B, McCance T (2006) Development of a framework for person-centred nursing. J Adv Nurs 56(5):472–479PubMedCrossRef McCormack B, McCance T (2006) Development of a framework for person-centred nursing. J Adv Nurs 56(5):472–479PubMedCrossRef
19.
Zurück zum Zitat Binnie A, Titchen A (1999) Freedom to practice: the development of patient-centred nursing. Heinemann, Oxford Binnie A, Titchen A (1999) Freedom to practice: the development of patient-centred nursing. Heinemann, Oxford
20.
Zurück zum Zitat Golderberg D, Williams P (1988) A user’s guide to the general health questionnaire. NFER-Nelson, Windsor, UK Golderberg D, Williams P (1988) A user’s guide to the general health questionnaire. NFER-Nelson, Windsor, UK
21.
Zurück zum Zitat Ferrell BR, Grant M, Chan J, Ahn C, Ferrell BA (1995) The impact of cancer pain education on family caregivers of elderly patients. Oncol Nurs Forum 22(8):1211–1218PubMed Ferrell BR, Grant M, Chan J, Ahn C, Ferrell BA (1995) The impact of cancer pain education on family caregivers of elderly patients. Oncol Nurs Forum 22(8):1211–1218PubMed
22.
Zurück zum Zitat Kristjanson LJ, Atwood J, Degner LF (1995) Validity and reliability of the family inventory of needs (FIN): measuring the care needs of families of advanced cancer patients. J Nurs Meas 3(2):109–126PubMed Kristjanson LJ, Atwood J, Degner LF (1995) Validity and reliability of the family inventory of needs (FIN): measuring the care needs of families of advanced cancer patients. J Nurs Meas 3(2):109–126PubMed
23.
Zurück zum Zitat Ritchie J, Spencer L, O’Connor W (2003) Carrying out qualitative analysis. In: Ritchie J, Lewis J (eds) Qualitative research practice. Sage, London, pp 219–262 Ritchie J, Spencer L, O’Connor W (2003) Carrying out qualitative analysis. In: Ritchie J, Lewis J (eds) Qualitative research practice. Sage, London, pp 219–262
24.
Zurück zum Zitat Cox K, Wilson E, Heath L, Collier J, Johnston I (2006) Preferences for follow-up after treatment for lung cancer. Cancer Nurs 29(3):176–187PubMedCrossRef Cox K, Wilson E, Heath L, Collier J, Johnston I (2006) Preferences for follow-up after treatment for lung cancer. Cancer Nurs 29(3):176–187PubMedCrossRef
25.
Zurück zum Zitat Osse B, Vernooij-Dassen M, Schade E, Grol R (2006) Problems experienced by the informal caregivers of cancer patients and their needs for support. Cancer Nurs 29(5):378–388PubMedCrossRef Osse B, Vernooij-Dassen M, Schade E, Grol R (2006) Problems experienced by the informal caregivers of cancer patients and their needs for support. Cancer Nurs 29(5):378–388PubMedCrossRef
26.
Zurück zum Zitat Kitson A (1999) The essence of nursing. Nurs Stand 13(23):42–46PubMed Kitson A (1999) The essence of nursing. Nurs Stand 13(23):42–46PubMed
27.
Zurück zum Zitat Moore S, Sherwin A, Medina J, Ream E, Plant H, Richardson A (2005) Caring for carers: a prospective audit of nurse specialist contact with families and carers of patients with lung cancer. Eur J Oncol Nurs 10:207–211PubMed Moore S, Sherwin A, Medina J, Ream E, Plant H, Richardson A (2005) Caring for carers: a prospective audit of nurse specialist contact with families and carers of patients with lung cancer. Eur J Oncol Nurs 10:207–211PubMed
28.
Zurück zum Zitat Hudson P (2004) A critical review of supportive interventions for family caregivers of patients with palliative-stage cancer. J Psychosoc Oncol 22(4):77–92CrossRef Hudson P (2004) A critical review of supportive interventions for family caregivers of patients with palliative-stage cancer. J Psychosoc Oncol 22(4):77–92CrossRef
29.
Zurück zum Zitat Northouse LL (2005) Helping families of patients with cancer. Oncol Nurs Forum 32(4):743–750PubMedCrossRef Northouse LL (2005) Helping families of patients with cancer. Oncol Nurs Forum 32(4):743–750PubMedCrossRef
30.
Zurück zum Zitat Blackwood B (2006) Methodological issues in evaluating complex healthcare interventions. J Adv Nurs 54(5):612–622PubMedCrossRef Blackwood B (2006) Methodological issues in evaluating complex healthcare interventions. J Adv Nurs 54(5):612–622PubMedCrossRef
31.
Zurück zum Zitat Morse J (2005) Evolving trends in qualitative research: advances in mixed method design. Qual Health Res 15(5):583–585PubMedCrossRef Morse J (2005) Evolving trends in qualitative research: advances in mixed method design. Qual Health Res 15(5):583–585PubMedCrossRef
32.
Zurück zum Zitat Dumont S, Turgeon J, Allard P, Gagnon P, Charbonneau C, Vezina L (2006) Caring for a loved one with advanced cancer: determinants of psychological distress in family caregivers. Journal of Palliative Medicine 9(4):912–921PubMedCrossRef Dumont S, Turgeon J, Allard P, Gagnon P, Charbonneau C, Vezina L (2006) Caring for a loved one with advanced cancer: determinants of psychological distress in family caregivers. Journal of Palliative Medicine 9(4):912–921PubMedCrossRef
Metadaten
Titel
Developing supportive care for family members of people with lung cancer: a feasibility study
verfasst von
Alison Richardson
Hilary Plant
Sally Moore
Jibby Medina
Amanda Cornwall
Emma Ream
Publikationsdatum
01.11.2007
Verlag
Springer-Verlag
Erschienen in
Supportive Care in Cancer / Ausgabe 11/2007
Print ISSN: 0941-4355
Elektronische ISSN: 1433-7339
DOI
https://doi.org/10.1007/s00520-007-0233-z

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