Results from the family and coping oriented palliative homecare intervention study (FamCope)—A randomized controlled trial

References

• Altman, D. G. (1991). Practical statistics for medical research (1st ed.). London: Chapman & Hall.
   Google Scholar
• Ammari, A. B. H., Hendriksen, C., & Rydahl-Hansen, S. (2015). Recruitment and reasons for non-participation in a family coping orientated palliative home care trial (FamCope). Journal of Psychosocial Oncology, 33(6), 655–674. doi:10.1080/07347332.2015.1082168
   PubMed Web of Science ®Google Scholar
• Applebaum, A. J., Lichtenthal, W. G., Pessin, H. A., Radomski, J. N., Gökbayrak, N. S., Katz, A. M., … Breitbart, W. (2012). Factors associated with attrition from a randomized controlled trial of meaning ‐ centered group psychotherapy for patients with advanced cancer. Psycho-Oncology, 21, 1195–1204.
   PubMed Web of Science ®Google Scholar
• Aaronson, A. N. K., Ahmedzai, S., Bergman, B., Bullinger, M., Cull, A., Duez, N. J., … Takeda, F. (1993). The European Organization for Research and Treatment of Cancer QLQ-C30: A Quality-of-Life Instrument for Use in International Clinical Trials in Oncology. Journal of the National Cancer Institute, 85, 365–376.
   PubMed Web of Science ®Google Scholar
• Badr, H., & Krebs, P. (2013). A systematic review and meta-analysis of psychosocial interventions for couples coping with cancer †. Psycho-Oncology, 22, 1688–1704.
   PubMed Web of Science ®Google Scholar
• Bakitas, M., Lyons, K. D., Hegel, M. T., Balan, S., Barnett, K. N., Brokaw, F. C., … Ahles, T. A. (2009). The project ENABLE II randomized controlled trial to improve palliative care for rural patients with advanced cancer: baseline findings, methodological challenges, and solutions. Palliative & Supportive Care, 7(1), 75–86. doi:10.1017/S1478951509000108
   PubMedGoogle Scholar
• Bakitas, M., Lyons, K. D., Hegel, M. T., Balan, S., Brokaw, F. C., Hull, J. G., … Ahles, T. A. (2013). Effects of a Palliative Care Intervention on Clinical Outcomes in Patients With Advanced Cancer. The Project ENABLE II Randomized Controlled Trial. JAMA, 302(7), 741–749.
   Google Scholar
• Bee, P. E., Barnes, P., & Luker, K. A. (2009). A systematic review of informal caregivers’ needs in providing home-based end-of-life care to people with cancer. Journal of Clinical Nursing, 18(10), 1379–1393. doi:10.1111/j.1365-2702.2008.02405.x
   PubMed Web of Science ®Google Scholar
• 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(2), 69–77. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11832252
   PubMed Web of Science ®Google Scholar
• Bjørner, J. B., Damsgaard, M. T., Watt, T., Bech, P., Rasmussen, N. K., Kristensen, T. S., … Thunedborg, K. (1997). Dansk manual til SF-36 – et spørgeskema om helbredsstatus. København: Lif Lægemiddelindustriforeningen.
   Google Scholar
• Bowman, K. F., Rose, J. H., Radziewicz, R. M., O'Toole, E. E., & Berila, R. A. (2009). Family caregiver engagement in a coping and communication support intervention tailored to advanced cancer patients and families. Cancer Nursing, 32(1), 73–81. doi:10.1097/01.NCC.0000343367.98623.83
   PubMed Web of Science ®Google Scholar
• Campbell, C. L., & Campbell, L. C. (2012). A systematic review of cognitive behavioral interventions in advanced cancer. Patient Education and Counseling, 89(1), 15–24. doi:10.1016/j.pec.2012.06.019
   PubMed Web of Science ®Google Scholar
• Carlson, L. E., Bultz, B. D., Speca, M., & Pierre, M. S. (2000). Partners of Cancer Patients : Part I. Impact, Adjustment, and Coping Across the Illness Trajectory. Journal of Psychosocial Oncology, 18(2), 39–63.
   Web of Science ®Google Scholar
• Fayers, P., Aaronson, N., Bjordal, K., Groenvold, M., Curran, D., & Bottomley, A. (2001). EORTC QLQ-C30 scoring manual (3rd ed.). Brussels: European Organisation for Research and Treatment of Cancer.
   Google Scholar
• Ferrario, S. R., Cardillo, V., Vicario, F., Balzarini, E., & Zotti, A. M. (2004). Advanced cancer at home: Caregiving and bereavement. Palliative Medicine, 18(2), 129–136. doi:10.1191/0269216304pm870oa
   PubMed Web of Science ®Google Scholar
• Ferris, F. D., Bruera, E., Cherny, N., Cummings, C., Currow, D., Dudgeon, D., … Von Roenn, J. H. (2009). Palliative cancer care a decade later: Accomplishments, the need, next steps – from the American Society of Clinical Oncology. Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology, 27(18), 3052–3058. doi:10.1200/JCO.2008.20.1558
   PubMed Web of Science ®Google Scholar
• Folkman, S., & Lazarus, R. S. (1988). The relationship between coping and emotion: Implications for theory and research. Social Science & Medicine, 26(3), 309–317.
   PubMed Web of Science ®Google Scholar
• Friedman, M. M., Bowden, V. R., & Jones, E. G. (2003). Family nursing. Research, theory and practice (5th ed.). New Jersey: Prentice Hall.
   Google Scholar
• Given, B. A., Given, C. W., & Kozachik, S. (2001). Family Support in Advanced Cancer. CA: A Cancer Journal for Clinicians, 51(4), 213–231. doi:10.3322/canjclin.51.4.213
   PubMed Web of Science ®Google Scholar
• Groenvold, M., Klee, M. C., Sprangers, M. A., & Aaronson, N. K. (1997). Validation of the EORTC QLQ-C30 quality of life questionnaire through combined qualitative and quantitative assessment of patient-observer agreement. Journal of Clinical Epidemiology, 50(4), 441–450. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/9179103
   PubMed Web of Science ®Google Scholar
• Grov, E. K., Dahl, A. A., Moum, T., & Fosså, S. D. (2005). Anxiety, depression, and quality of life in caregivers of patients with cancer in late palliative phase. Annals of Oncology : Official Journal of the European Society for Medical Oncology / ESMO, 16(7), 1185–1191. doi:10.1093/annonc/mdi210
   PubMed Web of Science ®Google Scholar
• 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), 1–30. doi:10.1037/0033-2909.134.1.1
   PubMed Web of Science ®Google Scholar
• Halyard, M. Y., & Ferrans, C. E. (2008). Quality-of-life assessment for routine oncology clinical practice. The Journal of Supportive Oncology, 6(5), 221–230.
   PubMedGoogle Scholar
• Hassanein, K. A., Musgrove, B. T., & Bradbury, E. (2001). Functional status of patients with oral cancer and its relation to style of coping, social support and psychological status. The British Journal of Oral & Maxillofacial Surgery, 39(5), 340–345. doi:10.1054/bjom.2001.0652
   PubMed Web of Science ®Google Scholar
• Higginson, I. J., & Carr, A. J. (2001). Using quality of life measures in the clinical setting. BMJ, 322, 1297–1300.
   PubMed Web of Science ®Google Scholar
• Hudson, P. L., Trauer, T., Graham, S., Grande, G., Ewing, G., Payne, S., … Thomas, K. (2010). A systematic review of instruments related to family caregivers of palliative care patients. Palliative Medicine, 24(7), 656–668. doi:10.1177/0269216310373167
   PubMed Web of Science ®Google Scholar
• Kershaw, T. S., Ellis, K., Yoon, H., Schafenacker, A. M., Katapodi, M. C., & Northouse, L. L. (2015). The interdependence of advanced cancer patients’ and their family caregivers’ mental health, physical health, and self-efficacy over time. Ann Behav Med, 49(6), 901–911.
   PubMed Web of Science ®Google Scholar
• Kershaw, T. S., Mood, D. W., Newth, G., Ronis, D. L., Sanda, M. G., Vaishampayan, U., & Northouse, L. L. (2008). Longitudinal analysis of a model to predict quality of life in prostate cancer patients and their spouses. Annals of Behavioral Medicine : A Publication of the Society of Behavioral Medicine, 36(2), 117–128. doi:10.1007/s12160-008-9058-3
   PubMed Web of Science ®Google Scholar
• King, M. T. (1996). The interpretation of scores from the EORTC quality of life questionnaire QLQ-C30. Quality of Life Research : An International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/8993101
   PubMedGoogle Scholar
• Koop, P. M., & Strang, V. R. (2011). The bereavement experience following home-based family caregiving for persons with advanced cancer. doi:10.1177/1054773803251364
   Google Scholar
• Kaasa, S., & Loge, J. H. (2002). Quality-of-life assessment in palliative care. The Lancet Oncology, 3(3), 175–182. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11902505
   PubMed Web of Science ®Google Scholar
• Lazarus, R. (1999). Stress and emotion – a new synthesis. London: Free Association Books.
   Google Scholar
• McCubbin, H. I. (1979). Integrating coping behavior in family stress theory. Journal of Marriage and Family, 41(2), 237–244.
   Web of Science ®Google Scholar
• McCubbin, H., Thompson, E., Thompson, A., & Fromer, J. (1998). Stress, coping and health in families: Sence of coherence and resiliency. Thousand Oaks, CA: Sage.
   Google Scholar
• Moyer, A., Sohl, S. J., Knapp-Oliver, S. K., & Schneider, S. (2009). Characteristics and methodological quality of 25 years of research investigating psychosocial interventions for cancer patients. Cancer Treatment Reviews, 35(5), 475–484. doi:10.1016/j.ctrv.2009.02.003
   PubMed Web of Science ®Google Scholar
• Neergaard, M. A., Olesen, F., Jensen, A. B., & Sondergaard, J. (2010). Shared care in basic level palliative home care: Organizational and interpersonal challenges. Journal of Palliative Medicine, 13(9), 1071–1077. doi:10.1089/jpm.2010.0036
   PubMed Web of Science ®Google Scholar
• Northouse, L. L., Kershaw, T., Mood, D., & Schafenacker, A. (2005). Effects of a family intervention on the quality of life of women with recurrent breast cancer and their family caregivers. Psycho-Oncology, 14(6), 478–491. doi:10.1002/pon.871
   PubMed Web of Science ®Google Scholar
• Northouse, L. L., Mood, D. W., Schafenacker, A., Kalemkerian, G., Zalupski, M., Lorusso, P., … Kershaw, T. (2013). Randomized clinical trial of a brief and extensive dyadic intervention for advanced cancer patients and their family caregivers. Psycho-Oncology, 22(January 2012), 555–563. doi:10.1002/pon
   PubMedGoogle Scholar
• Northouse, L. L., Mood, D. W., Schafenacker, A., Montie, J. E., Sandler, H. M., Forman, J. D., … Kershaw, T. (2007). Randomized clinical trial of a family intervention for prostate cancer patients and their spouses. Cancer, 110(12), 2809–2818. doi:10.1002/cncr.23114
   PubMed Web of Science ®Google Scholar
• Northouse, L. L., Rosset, T., Phillips, L., Mood, D., Schafenacker, A., & Kershaw, T. (2006). Research with families facing cancer : The challenges of accrual and retention Ã. Research in Nursing & Health, 29, 199–211. doi:10.1002/nur
   PubMed Web of Science ®Google Scholar
• Northouse, L. L., Walker, J., Schafenacker, A., Mood, D., Mellon, S., Galvin, E., … Freeman-Gibb, L. (2002). A family-based program of care for women with recurrent breast cancer and their family members. Oncology Nursing Forum, 29(10), 1411–1419. doi:10.1188/02.ONF.1411-1419
   PubMedGoogle Scholar
• O'Hara, R. E., Hull, J. G., Lyons, K. D., Bakitas, M., Hegel, M. T., Li, Z., & Ahles, T. A. (2010). Impact on caregiver burden of a patient-focused palliative care intervention for patients with advanced cancer. Palliative & Supportive Care, 8(4), 395–404. doi:10.1017/S1478951510000258
   PubMed Web of Science ®Google Scholar
• Olssøn, I., Mykletun, A., & Dahl, A. A. (2005). The Hospital Anxiety and Depression Rating Scale: a cross-sectional study of psychometrics and case finding abilities in general practice. BMC Psychiatry, 5, 46. doi:10.1186/1471-244X-5-46
   PubMed Web of Science ®Google Scholar
• Radbruch, L., & Payne, S. (2009). EAPC, White Paper on standards and norms for hospice and palliative care in Europe: Part 1. European Journal of Palliative Care, 16(6), 278–289.
   Google Scholar
• Radbruch, L., & Payne, S. (2010). EAPC, White Paper on standards and norms for hospice and palliative care in Europe: Part 2. European Journal of Palliative Care, 17(1), 22–33.
   Google Scholar
• Rainbird, K., Perkins, J., Sanson-Fisher, R., Rolfe, I., & Anseline, P. (2009). The needs of patients with advanced, incurable cancer. British Journal of Cancer, 101(5), 759–764. doi:10.1038/sj.bjc.6605235
   PubMed Web of Science ®Google Scholar
• Regan, T. W., Lambert, S. D., Girgis, A., Kelly, B., Kayser, K., & Turner, J. (2012). Do couple-based interventions make a difference for couples affected by cancer? A systematic review. BMC Cancer, 12(1), 279. doi:10.1186/1471-2407-12-279
   PubMedGoogle Scholar
• Rehse, B., & Pukrop, R. (2003). Effects of psychosocial interventions on quality of life in adult cancer patients: Meta analysis of 37 published controlled outcome studies. Patient Education and Counseling, 50(2), 179–186. doi:10.1016/S0738-3991(02)00149-0
   PubMed Web of Science ®Google Scholar
• Rydahl-Hansen, S. (2013). Conditions that are significant for advanced cancer patients’ coping with their suffering-as experienced by relatives. Journal of Psychosocial Oncology, 31(3), 334–355. doi:10.1080/07347332.2013.778933
   PubMed Web of Science ®Google Scholar
• Schofield, P., Ugalde, A., Carey, M., Mileshkin, L., Duffy, M., Ball, D., & Aranda, S. (2008). Lung cancer: Challenges and solutions for supportive care intervention research. Palliative & Supportive Care, 6(3), 281–287. doi:10.1017/S1478951508000424
   PubMedGoogle Scholar
• Snaith, R. P., & Zigmond, A. S. (1994). The hospital anxiety and depression scale manual. London: GL Assessment Limited.
   Google Scholar
• Soelver, L., Oestergaard, B., Rydahl-Hansen, S., & Wagner, L. (2012). Advanced cancer patients’ self-assessed physical and emotional problems on admission and discharge from hospital general wards–a questionnaire study. European Journal of Cancer Care, 21(5), 667–676. doi:10.1111/j.1365-2354.2012.01342.x
   PubMed Web of Science ®Google Scholar
• Steinhauser, K. E., Christakis, N. A., Clipp, E. C., & Mcintyre, L. (2000). Factors considered inportant at the end of life by patients, family, physicians, and other care providers. JAMA, 284(19), 2476–2482.
   PubMed Web of Science ®Google Scholar
• Strang, V. R., & Koop, P. M. (2003). Factors which influence coping: Home-based family caregiving of persons with advanced cancer. Journal of Palliative Care, 19(2), 107–114.
   PubMed Web of Science ®Google Scholar
• Thomsen, T. G., Hansen, S. R., & Wagner, L. (2011). How to be a patient in a palliative life experience? A qualitative study to enhance knowledge about coping abilities in advanced cancer patients. Journal of Psychosocial Oncology, 29(3), 254–273. doi:10.1080/07347332.2011.563345
   PubMed Web of Science ®Google Scholar
• Thomsen, T. G., Rydahl-Hansen, S., & Wagner, L. (2010). A review of potential factors relevant to coping in patients with advanced cancer. Journal of Clinical Nursing, 19(23–24), 3410–3426. doi:10.1111/j.1365-2702.2009.03154.x
   PubMed Web of Science ®Google Scholar
• Ware, J. E., & Sherbourne, C. D. (1992). The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Medical Care, 30(6), 473–483. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/1593914.
   PubMed Web of Science ®Google Scholar
• West, B. T., Welch, K. B., & Galechi, A. T. (2007). Linear mixed models: A practical guide using statistical software (2nd ed.). Chapman & Hall/CRC.
   Google Scholar
• Zigmond, A. S., & Snaith, R. P. (1983). The hospital Anxiety and Depression Scale. Acta Psychiatric Scandinavia, 67, 361–370.
   PubMed Web of Science ®Google Scholar