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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2018
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| 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 |