Thesis (M.A.)--University of Hong Kong, 2002. / Includes bibliographical references (leaves 61-66) Also available in print.

Thesis (M.P.A.)--University of Hong Kong, 1992. / Also available in print.

Thesis (M.P.A.)--University of Hong Kong, 2001. / Includes bibliographical references (leaves 93-96). Also available in print.

Thesis (M.P.A.)--University of Hong Kong, 2001. / Includes bibliographical references (leaves 148-162). Also available in print.

Thesis (M. Phil.)--University of Hong Kong, 2006. / Title proper from title frame. Also available in printed format.

(M.H.S.A.)--University of Alberta, 1997. / A thesis submitted to the Faculty of Graduate Studies and Research in partial fulfilment of the requirements for the degree of Master of Health Services Administration, Department of Public Health Sciences. Also available online.

Thesis (M.T.S.)--Catholic Theological Union, 1984. / Bibliography: leaves 43-45.

Background: Palliative care means improving quality of life along a spectrum of illnesses including cancer. Cancer is one of the leading causes of death. Having the discussion of goals of care including palliative care is important to have with individuals who have advanced cancer. There were limited studies that identify the providers’ attitudes, subjective norms, and perceived behavioral control on discussion of goals of care including palliative care. Purpose/Aim: This Doctoral Project consisted of identifying factors (i.e., attitudes, behaviors and subjective norms) in discussion of goals of care with their terminal cancer patients in the outpatient oncology clinic. Multiple studies have demonstrated the lack of knowledge providers have about palliative care. Through this study, the attitudes, subjective norms, and behaviors of providers were evaluated regarding goals of care for palliative care. Methods: An investigator developed questionnaire with six-point Likert-type scaling was used to measure each dimension (attitudes, subjective norms, and perceived behavioral control) regarding discussion of goals regarding care. These questionnaires were sent electronically to the oncology providers at Arizona Center for Cancer Care in Phoenix, Arizona. The data were collected through Qualtrics. Outcomes: Six providers participated in the survey. Results on the Attitude subscale indicated that the providers regarded discussing goals of care including palliative as very important and beneficial to patients. In comparison to this subscale score, the results on the Subjective Norms and Perceived Behavioral Control subscales were somewhat lower, though still above the mean, indicating that providers regarded the norm and level of resources available for discussing goals of care as somewhat lacking in their work setting. Further research is needed in this area of inquiry, including a quality improvement project to promote quality care in discussing goals of care including palliative care with patients who are diagnosed with advanced cancer.

No description available.

M.Sc.(Nursing), Faculty of Health Sciences, University of the Witwatersrand, 2012 / The purpose of this study was to describe family members’ opinions regarding the quality of care and decision-making in the adult intensive care units. A quantitative descriptive research design was utilized to meet the study objectives. Structured interviews were conducted using the FS-ICU (24) questionnaire with participants (family members, n=100) drawn from three intensive care units. Descriptive and comparative statistics were used to analyse the data. Satisfaction with care was rated by family members’ as higher than their satisfaction with decision-making. Overall 91.0% (n=91) of family members’ were mostly satisfied with the care provided. Of the 24 items the management of patient symptoms was the most highly rated items. The least satisfied item related to the waiting room, which was rated as 93.0% (n=93) dissatisfactory. Frequency of communication, completeness of information, feeling excluded and unsupported during decision-making and the rigid visiting hours were areas identified for improvement in the ICU. These findings suggest that deficiencies exist in meeting family’ needs. Based on the research findings, it can be concluded that results of this study have supported the existing evidence in literature from previous studies on family satisfaction with care and decision-making in the ICU. Recommendations for nursing practice, education, research and institution are proposed.