Family Caregiver Participation in Palliative Care Research: Challenging the Myth
Context: Despite international guidelines emphasizing consumer-directed care and autonomous decisions in research participation, there is a common myth that research can be an additional and unwanted burden on patients and their family members. Objectives: To examine the experiences and impact of re...
| Main Authors: | , , , |
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| Format: | Journal Article |
| Published: |
Elsevier
2017
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| Online Access: | http://purl.org/au-research/grants/arc/LP110100622 http://hdl.handle.net/20.500.11937/51551 |