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Pragmatic Randomized Clinical Trials

- Using Primary Data Collection and Electronic Health Records

Om Pragmatic Randomized Clinical Trials

Pragmatic Randomized Clinical Trials Using Primary Data Collection and Electronic Health Records addresses the practical aspects and challenges of the design, implementation, and dissemination of pragmatic randomized trials, also sometimes referred to as practical or hybrid randomized trials. While less restrictive and more generalizable than traditional randomized controlled trials, such trials have specific challenges which are addressed in this book. The book contains chapters encompassing common designs along with advantages and limitations of such designs, analytic aspects in planning trials and estimating sample size, and how to use patient partners to help design and operationalize pragmatic randomized trials. Pragmatic trials conducted using primary data collection and trials embedded in electronic health records - including electronic medical records and administrative insurance claims - are addressed. This comprehensive resource is valuable not only for pharmacoepidemiologists, biostatisticians and clinical researchers, but also across the biomedical field for those who are interested in applying pragmatic randomized clinical trials in their research. ΓÇó Addresses typical designs and challenges of pragmatic randomized clinical trials (pRCTs) ΓÇó Encompasses analytic aspects of such trials ΓÇó Discusses real cases on operational challenges in launching and conducting pRCTs in electronic health records

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  • Språk:
  • Engelsk
  • ISBN:
  • 9780128176634
  • Bindende:
  • Paperback
  • Sider:
  • 498
  • Utgitt:
  • 14. april 2021
  • Dimensjoner:
  • 234x191x27 mm.
  • Vekt:
  • 1006 g.
  Gratis frakt
Leveringstid: 2-4 uker
Forventet levering: 13. mars 2026

Beskrivelse av Pragmatic Randomized Clinical Trials

Pragmatic Randomized Clinical Trials Using Primary Data Collection and Electronic Health Records addresses the practical aspects and challenges of the design, implementation, and dissemination of pragmatic randomized trials, also sometimes referred to as practical or hybrid randomized trials. While less restrictive and more generalizable than traditional randomized controlled trials, such trials have specific challenges which are addressed in this book.
The book contains chapters encompassing common designs along with advantages and limitations of such designs, analytic aspects in planning trials and estimating sample size, and how to use patient partners to help design and operationalize pragmatic randomized trials. Pragmatic trials conducted using primary data collection and trials embedded in electronic health records - including electronic medical records and administrative insurance claims - are addressed.
This comprehensive resource is valuable not only for pharmacoepidemiologists, biostatisticians and clinical researchers, but also across the biomedical field for those who are interested in applying pragmatic randomized clinical trials in their research.

ΓÇó Addresses typical designs and challenges of pragmatic randomized clinical trials (pRCTs) ΓÇó Encompasses analytic aspects of such trials ΓÇó Discusses real cases on operational challenges in launching and conducting pRCTs in electronic health records

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