Pragmatic randomised clinical trials using electronic health records: general practitioner views on a model of a priori consent

Pragmatic randomised clinical trials could use existing electronic health records (EHRs) to identify trial participants, perform randomisation, and to collect follow-up data. Achieving adequate informed consent in routine care and clinician recruitment have been identified as key barriers to this ap...

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Detalles Bibliográficos
Autores principales: Hills, Thomas, Semprini, Alex, Beasley, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956547/
https://www.ncbi.nlm.nih.gov/pubmed/29769088
http://dx.doi.org/10.1186/s13063-018-2658-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956547/
https://www.ncbi.nlm.nih.gov/pubmed/29769088
http://dx.doi.org/10.1186/s13063-018-2658-8

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