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Psychometric evaluation of a Czech version of the Family Inventory of Needs

Published online by Cambridge University Press:  16 September 2015

Radka Bužgová  and
Radka Kozáková
Radka Bužgová
Affiliation:
Department of Nursing and Midwifery, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic
Radka Kozáková*
Affiliation:
Department of Nursing and Midwifery, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic
*
Address correspondence and reprint request to: Radka Bužgová, Department of Nursing and Midwifery, Faculty of Medicine, University of Ostrava, UOM LF OU, Syllabova 19, 700 30 Ostrava, Czech Republic. E-mail: [email protected].
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Abstract

Objective:

Identification of areas that family members consider important and in which they need help and support is one of the main goals of palliative care. Our research aimed to assess the psychometric properties of a Czech version of the Family Inventory of Needs (FIN).

Method:

The group comprised 272 family members of terminally ill cancer patients at the University Hospital in Ostrava. Reliability was assessed by internal consistency (Cronbach's alpha), test–retest reliability, and correlation of both scales and items within the scales (item–total correlation). To verify construct validity, exploratory factor analysis and principal component analysis with a varimax rotation were utilized.

Results:

Using exploratory factor analysis, the following four factors (domains) were extracted: basic information, information on treatment and care, support, and comfort of the patient. Cronbach's α for the entire questionnaire was 0.924 on the importance scale and 0.912 for the satisfaction scale; for all domains, a value of α greater than 0.7 was ascertained. Test–retest reliability was also higher than 0.7 for all domains. On the satisfaction scale, a moderate correlation was confirmed between unmet needs in the domains basic information, support, and comfort of the patient, and the total score, and in selected quality-of-life domains.

Significance of results:

The results of tests on the psychometric properties of the FIN questionnaire demonstrated at least satisfactory validity and reliability, and confirmed that it can be employed to assess the needs of palliative care patients in the Czech Republic.

Keywords

Palliative careFamilyNeeds assessmentValidityReliability
Type
Original Articles
Information
Palliative & Supportive Care , Volume 14 , Issue 2: Measurement Development in Palliative and Supportive Care , April 2016 , pp. 142 - 150
Copyright
Copyright © Cambridge University Press 2015 

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References

REFERENCES

Bandari, R., Majideh, H. & Nahid, R. (2014). Psychometric properties of the Persian version of the Critical Care Family Needs Inventory. The Journal of Nursing Research, 22, 259–267.CrossRefGoogle ScholarPubMed
Borneman, T., Chu, D., Wagman, L., et al. (2003). Concerns of family caregivers of patients with cancer facing palliative surgery for advanced malignancies. Oncology Nursing Forum, 30, 997–1005.CrossRefGoogle ScholarPubMed
Boyle, D., Blodgett, L., Gnesdiloff, S., et al. (2000). Caregiver quality of life after autologous bone marrow transplantation. Cancer Nursing, 23, 193–203.CrossRefGoogle ScholarPubMed
Brener, T.H. (2007). End of life: A nurse's guide to compassionate care. Philadelphia: Lippincott Williams & Wilkins: Ambler.Google Scholar
Bužgová, R., Kozáková, R., Sikorová, L., et al. (2015). Development and psychometric evaluation of patient needs assessment in a palliative care (PNAP) instrument. Palliative & Supportive Care, 14, 129–137.CrossRefGoogle Scholar
Chien, W., Ip, W., Lee, I.Y.M. (2005). Psychometric properties of a Chinese version of the Critical Care Family Needs Inventory. Research in Nursing & Health, 28, 474–487.CrossRefGoogle ScholarPubMed
Cohen, R., Leis, A.M. & Kuhl, D. (2006). QOLLTI–F: Measuring family carer quality of life. Palliative Medicine, 20, 755–767.CrossRefGoogle ScholarPubMed
Crowe, H. & Costello, A.J. (2003). Prostate cancer: Perspectives on quality of life and impact of treatment on patients and their partners. Urologic Nursing, 23, 279–285.Google ScholarPubMed
Dawson, N.J. (1991). Need satisfaction in terminal care settings. Social Science & Medicine, 32, 83–87.CrossRefGoogle ScholarPubMed
Deeken, J.F., Taylor, K.L., Mangan, P., et al. (2003). Care for the caregivers: A review of self-report instruments developed to measure the burden, needs, and quality of life of informal caregivers. Journal of Pain and Symptom Management, 26, 922–953.CrossRefGoogle ScholarPubMed
Ewing, G. & Grande, G. (2013). Development of a Career Support Needs Assessment Tool (CSNAT) for end-of-life care practice at home: A qualitative study. Palliative Medicine, 27, 244–256.CrossRefGoogle Scholar
Fridriksdóttir, N., Sigurdardottir, V. & Gunnarsdottir, S. (2006). Important needs of families in acute and palliative care settings assessed with the Family Inventory of Needs. Palliative Medicine, 20, 425–432.CrossRefGoogle ScholarPubMed
Fridriksdóttir, N., Saevarsdóttir, T., Halfdánardóttir, S.Í., et al. (2011). Family members of cancer patients: Needs, quality of life and symptoms of anxiety and depression. Acta Oncologica, 50, 252–258.CrossRefGoogle ScholarPubMed
Garre-Olmo, J., Planas-Pujol, X., López-Pousa, S., et al. (2010). Cross-cultural adaptation and psychometric validation of a Spanish version of the Quality of Life in Late-Stage Dementia Scale. Quality of Life Research, 19, 445–453.CrossRefGoogle ScholarPubMed
Gómez-Martíinez, S., Arnal, R.B. & Juliá, B.G. (2011). The short version of the Critical Care Family Needs Inventory (CCFNI): Adaptation and validation for a Spanish sample. Anales del Sistema Sanatario de Navarra, 34, 349–361.Google ScholarPubMed
Guyatt, G.H., Feeny, D.H. & Patrick, D.L. (1993). Measuring health-related quality of life. Annals of Internal Medicine, 118, 622–629.CrossRefGoogle ScholarPubMed
Harding, R. & Higginson, I. (2003). What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliative Medicine, 17, 63–74.CrossRefGoogle ScholarPubMed
Hendl, J. (2006). Přehled statistických metod zpracování dat. Praha: Portál.Google Scholar
Hileman, J.W., Lackey, M.R. & Hassanein, R.S. (1992). Identifying the needs of home caregivers of patients with cancer. Oncology Nursing Forum, 19, 771–777.Google ScholarPubMed
Kilpatrick, M.G., Kristjanson, L.J. & Tataryn, D. (1998). Measuring the information needs of husbands of women with breast cancer: Validity and reliability of the Family of Inventory of Needs–Husbands. Oncology Nursing Forum, 25, 1347–1351.Google ScholarPubMed
Kristjanson, L.J. & White, K. (2002). Clinical support for families in the palliative care phase of hematologic or oncologic illness. Hematology/Oncology Clinics of North America, 16, 45–76.CrossRefGoogle ScholarPubMed
Kristjanson, L.J., Atwood, J. & Degner, L.F. (1995). Validity and reliability of the Family Inventory of Needs (FIN): Measuring the care needs of families of advanced cancer patients. Journal of Nursing Measurement, 3, 109–126.CrossRefGoogle ScholarPubMed
Longman, J., Atwood, J.R., Sherman, J.B., et al. (1992). Care needs of home-based cancer patients and their cancer patients and their caregivers: Quantitative findings. Cancer Nursing, 15, 182–190.CrossRefGoogle ScholarPubMed
Macey, B.A. & Bouman, C.C. (1991). An evaluation of the validity, reliability, and readability of the Critical Care Family Needs Inventory. Heart & Lung, 20, 398–403.Google ScholarPubMed
Meyers, J.M. & Gray, L.N. (2001). The relationships between family primary caregiver characteristics and satisfaction with hospice care, quality of life, and burden. Oncology Nursing Forum, 28, 73–82.Google ScholarPubMed
McMillan, S.C. & Weitzner, M.A. (2003). Methodological issues in collecting data from debilitated patients with cancer near the end of life. Oncology Nursing Forum, 30, 123–129.CrossRefGoogle ScholarPubMed
Nunnally, J.C. (1978). Psychometric theory. New York: McGraw–Hill.Google Scholar
Osse, B.H., Vernooij-Dassen, M.J., de Vree, B.P., et al. (2000). Assessment of the need for palliative care as perceived by individual cancer patients and their families: A review of instruments for improving patient participation in palliative care. Cancer, 88, 900–911.3.0.CO;2-2>CrossRefGoogle ScholarPubMed
Peters, L. & Sellick, K. (2006). Quality of life of cancer patients receiving inpatient and home-based palliative care. Journal of Advanced Nursing, 12, 524–533.CrossRefGoogle Scholar
Serio, C.D., Kreutzer, J.S. & Witol, A.D. (1997). Family needs after traumatic brain injury: A factor-analytic study of the Family Needs Questionnaire. Brain Injury, 11, 1–9.CrossRefGoogle ScholarPubMed
Schaffer, R. (1953). Job satisfaction as related to need satisfaction in work. Psychological Monographs, 67, 364.CrossRefGoogle Scholar
Sláma, O., Kabelka, L. & Špinková, M. (2013). Paliativní péče v ČR v roce 2013. Praha a Brno: Perspektiva České společnosti paliativní medicíny ČLS JEP.Google Scholar
Streiner, D.L. & Norman, G.R. (2003). Health measurement scales: A practical guide to their development and use. New York: Oxford University Press.CrossRefGoogle Scholar
Terwee, C.B., Bot, S.D., de Boer, M.R., et al. (2007). Quality criteria were proposed for measurement properties of health status questionnaires. Journal of Clinical Epidemiology, 60, 34–42.CrossRefGoogle ScholarPubMed
Tringali, C.A. (1986). The needs of family members of cancer patients. Oncology Nursing Forum, 13, 65–70.Google ScholarPubMed
Waller, A., Girgi, A., Lecathelinais, C., et al. (2010). palliative care research program team: Validity, reliability and clinical feasibility of a needs assessment tool for people with progressive cancer. Psycho-Oncology, 19, 726–733.CrossRefGoogle ScholarPubMed
Ware, J.E. & Gandek, B. (1998). Methods for testing data quality, scaling assumptions, and reliability: The IQOLA Project approach. International Quality of Life Assessment. Journal of Clinical Epidemiology, 51, 945–952.CrossRefGoogle ScholarPubMed
Wen, K.Y. & Gustafson, D.H. (2004). Needs assessment for cancer patients and their families. Health and Quality of Life Outcomes, 2, 1–12.CrossRefGoogle ScholarPubMed
Wennman-Larsen, A. & Tishelman, C. (2002). Advanced home care for cancer patients at the end of life: A qualitative study of hopes and expectations of family caregivers. Scandinavian Journal of Caring Science, 16, 240–247.CrossRefGoogle ScholarPubMed
Wright, K. & Dyck, S. (1984). Expressed concerns of adult cancer patients' family members. Cancer Nursing, 6, 371–374.Google Scholar