Skip navigation
  • Home
  • Browse
    • Communities
      & Collections
    • Browse Items by:
    • Publication Date
    • Author
    • Title
    • Subject
    • Department
  • Sign on to:
    • My MacSphere
    • Receive email
      updates
    • Edit Profile


McMaster University Home Page
  1. MacSphere
  2. Open Access Dissertations and Theses Community
  3. Open Access Dissertations and Theses
Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/12633
Full metadata record
DC FieldValueLanguage
dc.contributor.advisorBrazil, Kevinen_US
dc.contributor.advisorMacMillan, Harrieten_US
dc.contributor.advisorLohfeld, Lynneen_US
dc.contributor.authorO`Brien, Valerie A.en_US
dc.date.accessioned2014-06-18T17:00:13Z-
dc.date.available2014-06-18T17:00:13Z-
dc.date.created2012-09-26en_US
dc.date.issued2012-10en_US
dc.identifier.otheropendissertations/7501en_US
dc.identifier.other8561en_US
dc.identifier.other3351427en_US
dc.identifier.urihttp://hdl.handle.net/11375/12633-
dc.description.abstract<p>Introduction: Palliative care in Canada is an under-funded service for all Canadians, but for Aboriginal people in Canada, the level of access to such care is significantly lower. This study examined the system of palliative care delivery at Six Nations of the Grand River. The overall aim of the project was to identify ways on how the system of care could be improved.</p> <p>Methods: A qualitative case study approach was used. Interviews were held with Elders and family caregivers to identify the priorities in care delivery from their perspective. Focus groups were held with representatives from palliative care service provider agencies in an effort to identify the strengths and challenges within the system and to determine how palliative care services provided to the members of Six Nations could be improved.</p> <p>Findings: Themes identified in the interviews included: personable, caring care; culturally-competent care; open two-way communication; support for family caregivers; palliative home care should be available; meeting comfort needs of the person; and the need for a hospice in the community. The main theme identified in the focus groups with care providers included: relationship/rapport issues between provider organizations; within-program strengths and challenges; cultural considerations in care; and broader system factors that influence care.</p> <p>Discussion: Relationship/rapport issues were identified as a challenge, and it appeared that the focus groups provided an opportunity for communication between the organizations to improve. Identification of within-program challenges – and ways to address these challenges - may provide opportunities for each organization to improve how palliative care services are delivered at Six Nations. Identification of broader system factors that influence care may also benefit patients in need of palliative care.</p>en_US
dc.subjectAboriginalen_US
dc.subjectFirst Nationsen_US
dc.subjectPalliative Careen_US
dc.subjectEnd-of-Lifeen_US
dc.subjectHealth Policyen_US
dc.subjectOther Medicine and Health Sciencesen_US
dc.subjectHealth Policyen_US
dc.titlePerson Centred Palliative Care: A First Nations Perspectiveen_US
dc.typethesisen_US
dc.contributor.departmentHealth Research Methodologyen_US
dc.description.degreeMaster of Science (MSc)en_US
Appears in Collections:Open Access Dissertations and Theses

Files in This Item:
File SizeFormat 
fulltext.pdf
Open Access
630.45 kBAdobe PDFView/Open
Show simple item record Statistics


Items in MacSphere are protected by copyright, with all rights reserved, unless otherwise indicated.

Sherman Centre for Digital Scholarship     McMaster University Libraries
©2022 McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L8 | 905-525-9140 | Contact Us | Terms of Use & Privacy Policy | Feedback

Report Accessibility Issue