Introduzione

Understanding the role of statistics and statisticians in protocol planning, report review or publication submission, is essential to produce an effective document.
The course aims at increasing knowledge of basic statistical principles by analysing case studies (study protocol and/or scientific articles) to establish shared concepts.

During the training the following topics will be discussed:

  • Measures of risk: Odds Ratio, Hazard Ratio, Absolute Risk, NNT
  • Observational studies: how they are constructed, which patients they include, the difference between prospective and retrospective studies and quality assessment
  • Multivariate analyses: logistic regression, multivariate Cox analysis and propensity score
  • How to read an observational study
  • Randomised trials (RCTs): history, superiority and non-inferiority studies, quality assessment
  • Blinding, sample size calculation and the difference between pharmacological and non-pharmacological RCTs
  • How to read a randomised trial
  • Exercise on practical examples proposed by the trainees or by the lecturer.

The course is addressed to clinical operation manager, clinical study coordinator, CRAs, medical affairs manager, medical science liaison and anyone who wants to improve knowledge in the field.

 

Participant’s experience

Participants should have familiarity with the basic principles governing clinical trials and the elements necessary to define a study protocol.

 

The online course includes theoretical lectures and exercises on practical examples proposed by the trainees or the lecturer.

Docente/i
Fabrizio D'Ascenzo
Info

Fabrizio D'Ascenzo

Medical Doctor at Division of Cardiology, Department of Medical Science, Città della Salute e della Scienza, Turin
Dr D’Ascenzo works as researcher and interventional cardiologist in the Division of Cardiology of the University of Turin. His main interests of research range from management of Acute Coronary Syndromes (ACSs) both from an interventional point of view and secondary prevention to Transcatheter Aortic Valve Implantation (TAVI) focusing in particular on the impact of Artificial Intelligence (AI) on medicine. He has publishes over 300 papers with an H-Index of 45 (Scopus). He has taught several courses on statistics for non-statisticians, medical reading/writing combining both clinical and scientific skills.

Online Training – 3 modules

MODULE 1 | 09 November 2022 from 2 pm to 5 pm CET

MODULE 2 | 16 November 2022 from 2 pm to 5 pm CET

MODULE 3 | 23 November 2022 from 2 pm to 5 pm CET

 

After the registration, you will receive all details about the connection.

The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.

Early Bird: € 890,00* (until 12 October 2022)

Ordinary: € 1090,00*

Freelance – Academy – Public Administration**: € 580,00*

* for Italian companies: +22% VAT

** Early Bird discount not applicable to Freelance – Academy – Public Administration fee

The fee includes: tuition, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.

Versione Stampabile
Cosa saprai fare dopo il corso
Risultato atteso
Interact and communicate more efficiently with statisticians when planning protocols, reviewing reports, or submitting publications
Risultato atteso
Critically evaluate the methods and results of a study reported in a Clinical Study Report or a scientific publication

<p><span>Online interactive training on Zoom platform. </span></p>
<p><em>LS Academy will provide the access link to the virtual platform a few days before the training.</em></p>

Online interactive training on Zoom platform. 

LS Academy will provide the access link to the virtual platform a few days before the training.

<p><span>Online interactive training on Zoom platform. </span></p>
<p><em>LS Academy will provide the access link to the virtual platform a few days before the training.</em></p>

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