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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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| Publicado no: | Res Involv Engagem |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5611637/ https://ncbi.nlm.nih.gov/pubmed/29062497 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40900-015-0006-7 |
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