Thoughts on reporting public and patient engagement and involvement in research in the Journal of Advanced Nursing (Editorial)
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Dale, Craig M
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Abstract
Historically, patient stakeholders (patients, families and caregivers) have been the subject of research, mere datapoints in the research enterprise. Researchers used participants' data and rarely considered other contributions they could offer. Over the last 15 years, this perspective has changed, as researchers and funding agencies now acknowledge that patients and the public have capacity to design, implement and share relevant and meaningful research (Manafo et al., 2018).
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Journal of Advanced Nursing
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78
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12
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© 2022 John Wiley & Sons Ltd. This is the peer reviewed version of the following article: Thoughts on reporting public and patient engagement and involvement in research in the Journal of Advanced Nursing, Journal of Advanced Nursing, 78 (12), pp. e152-e154, which has been published in final form at https://doi.org/10.1111/jan.15410. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.
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Nursing
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Life Sciences & Biomedicine
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Tobiano, G; Dale, CM, Thoughts on reporting public and patient engagement and involvement in research in the Journal of Advanced Nursing (Editorial), Journal of Advanced Nursing, 2022, 78 (12), pp. E152-E154