Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2407-11-298
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dc.titleMeasuring cancer care coordination: Development and validation of a questionnaire for patients
dc.contributor.authorYoung, J.M
dc.contributor.authorWalsh, J
dc.contributor.authorButow, P.N
dc.contributor.authorSolomon, M.J
dc.contributor.authorShaw, J
dc.date.accessioned2020-10-27T11:31:57Z
dc.date.available2020-10-27T11:31:57Z
dc.date.issued2011
dc.identifier.citationYoung, J.M, Walsh, J, Butow, P.N, Solomon, M.J, Shaw, J (2011). Measuring cancer care coordination: Development and validation of a questionnaire for patients. BMC Cancer 11 : 298. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2407-11-298
dc.identifier.issn14712407
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181631
dc.description.abstractBackground: Improving the coordination of cancer care is a priority area for service improvement. However, quality improvement initiatives are hindered by the lack of accurate and reliable measures of this aspect of cancer care. This study was conducted to develop a questionnaire to measures patients' experience of cancer care coordination and to assess the psychometric properties of this instrument.Methods: Questionnaire items were developed on the basis of literature review and qualitative research involving focus groups and interviews with cancer patients, carers and clinicians. The draft instrument was completed 686 patients who had been recently treated for a newly diagnosed cancer, including patients from metropolitan, regional and rural areas of New South Wales, Australia. To assess test-retest reliability, 119 patients completed the questionnaire twice. Unreliable items those with limited variability or high levels of missing data were eliminated. Exploratory factor analysis was conducted to define the underlying factor structure of the remaining items and subscales were constructed. Correlations between these and global measures of the experience of care coordination and the quality of care were assessed.Results: Of 40 items included in the draft questionnaire, 20 were eliminated due to poor test-retest reliability (n = 4), limited response distributions (n = 8), failure to load onto a factor (n = 7) or detrimental effect on the internal consistency of the scale (n = 1). The remaining 20 items loaded onto two factors named 'Communication' and 'Navigation', which explained 91% of the common variance. Internal consistency was with high for the instrument (Cronbach's alpha 0.88) and each subscale (Cronbach's alpha 0.87 and 0.73 respectively). There was no apparent 'floor' or 'ceiling' effect for the total score or the Communication subscale, but evidence of a ceiling effect for the Navigation subscale with 21% of respondents achieving the highest possible score. There were moderate positive associations between the total score and global measures of care coordination (r = 0.57) and quality of care (r = 0.53).Conclusions: The instrument developed in this study demonstrated consistency and robust psychometric properties. It may provide a useful tool to measure patients' experience of cancer care coordination in future surveys and intervention studies. © 2011 Young et al; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectadult
dc.subjectaged
dc.subjectarticle
dc.subjectAustralia
dc.subjectcancer care coordination
dc.subjectCancer Care Coordination Questionnaire for Patients
dc.subjectconstruct validity
dc.subjectfactorial analysis
dc.subjectfemale
dc.subjecthealth care concepts
dc.subjecthealth care quality
dc.subjecthuman
dc.subjectinternal consistency
dc.subjectmale
dc.subjectpatient care
dc.subjectpsychometry
dc.subjectquestionnaire
dc.subjecttest retest reliability
dc.subjecthealth care quality
dc.subjecthealth care survey
dc.subjectmethodology
dc.subjectmiddle aged
dc.subjectneoplasm
dc.subjectreproducibility
dc.subjectstandard
dc.subjectstatistics
dc.subjectvalidation study
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectFemale
dc.subjectHealth Care Surveys
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNeoplasms
dc.subjectNew South Wales
dc.subjectPsychometrics
dc.subjectQuality of Health Care
dc.subjectQuestionnaires
dc.subjectReproducibility of Results
dc.subjectYoung Adult
dc.typeArticle
dc.contributor.departmentSURGERY
dc.description.doi10.1186/1471-2407-11-298
dc.description.sourcetitleBMC Cancer
dc.description.volume11
dc.description.page298
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