Community-based participatory research in palliative care: a social justice imperative
- PMID: 35122757
- PMCID: PMC9260493
- DOI: 10.1016/S2468-2667(21)00305-4
Community-based participatory research in palliative care: a social justice imperative
Conflict of interest statement
We declare no competing interests.
Comment on
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Access to palliative care: the primacy of public health partnerships and community participation.Lancet Public Health. 2021 Nov;6(11):e791-e792. doi: 10.1016/S2468-2667(21)00213-9. Epub 2021 Oct 9. Lancet Public Health. 2021. PMID: 34634238 No abstract available.
References
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- Mills J, Abel J, Kellehear A, Patel M. Access to palliative care: the primacy of public health partnerships and community participation. Lancet Public Health 2021; 6: e791. - PubMed
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- Suarez-Balcazar Y. Meaningful Engagement in research: community residents as co-creators of knowledge. Am J Community Psychol 2020; 65: 261–71. - PubMed
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- Elk R, Emanuel L, Hauser J, Bakitas M, Levkoff S. Developing and testing the feasibility of a culturally based tele-palliative care consult based on the cultural values and preferences of southern, rural African American and white community members: a program by and for the community. Health Equity 2020; 4: 52–83. - PMC - PubMed
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- Elk R, Barnett M, Thompson M, Tate V, Nichols A. African American communities speak to palliative care clinicians: evaluation of an innovative community-developed communication skills training program (GP726). J Pain Symptom Manage 2020; 60: 260–61.
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- WHO. Assessing the Development of palliative care worldwide: a set of actionable indicators. Geneva: World Health Organization, 2021.
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