Patient and public involvement in data collection for health services research: a descriptive study

PLAIN ENGLISH SUMMARY: There is a consensus that patients and the public should be involved in research in a meaningful way. To date, lay people have been mostly involved in developing research ideas and commenting on patient information but not as much in actual data collection. We have had firstha...

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Detalles Bibliográficos
Autores principales: Garfield, Sara, Jheeta, Seetal, Jacklin, Ann, Bischler, Anna, Norton, Christine, Franklin, Bryony D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611637/
https://www.ncbi.nlm.nih.gov/pubmed/29062497
http://dx.doi.org/10.1186/s40900-015-0006-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611637/
https://www.ncbi.nlm.nih.gov/pubmed/29062497
http://dx.doi.org/10.1186/s40900-015-0006-7

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