Co-designing new tools for collecting, analysing and presenting patient experience data in NHS services: working in partnership with patients and carers
Plain English summary The way we collect and use patient experience data is important because of concern that patients and carers may be excluded by the limited ways it is currently done in NHS services. In this study, we worked in partnership with researchers, staff, patient and carer participants,...
Guardado en:
Autores principales: | Nicola Small, Bie Nio Ong, Annmarie Lewis, Dawn Allen, Nigel Bagshaw, Papreen Nahar, Caroline Sanders, the DEPEND team |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
BMC
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/882ea802c14642c1825dc9077930c7af |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Pushing the boundaries of patient experience
por: Jason Wolf
Publicado: (2017) -
Patient partner compensation in research and health care: the patient perspective on why and how
por: Dawn Richards, et al.
Publicado: (2018) -
Development and evaluation of a virtual patient-centered outcomes research training program for the cystic fibrosis community
por: Emily M. Godfrey, et al.
Publicado: (2021) -
NHS England Always Events® program: Developing a national model for co-production
por: Claire Marshall, et al.
Publicado: (2019) -
Cancer follow-up supported by patient-reported outcomes in patients undergoing intended curative complex surgery for advanced cancer
por: Sissel Ravn, et al.
Publicado: (2021)