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GCR Connect webinar – Bad statistics in medical research

Home All news & events Events GCR Connect webinar – Bad statistics in…

 

When    Thursday 14 March 2024, 3pm – 4pm (AEDT)
Where    Online.
Registration   Registration is available here.


Bad statistics in medical research, Prof Adrian Barnett, Queensland University of Technology

Abstract:
Using the wrong statistical methods can completely invalidate a study’s results, potentially wasting years of hard work, misdirecting future research, and misinforming health policy. Despite the importance of statistics many medical researchers do not have adequate training and/or access to a qualified statistician. Medical researchers often attempt complex study designs that require advanced statistical knowledge. For example, a review of 606 published prediction models for COVID-19 found only 7 of the 606 models were potentially useful for practice, with many using statistical methods that were inappropriate and/or badly described. I will make the case for researchers to use simple study designs that only require basic statistical methods. I will discuss the potential for automated statistical reviews to improve research quality and the need for more training in research methods.

Bio of Professor Adrian Barnett:
Adrian is a professor of statistics who has worked for over 29 years in health and medical research. He was the president of the Statistical Society of Australia from 2018 to 2020. His current research concerns improving statistical practice to reduce research waste. He is the president of the Association for Interdisciplinary Meta-Research and Open Science, whose mission is to improve research quality.


About GCR Connect:

GCR Connect is a network of Genetic Counsellors working in research roles across Australasia and beyond. Established in July 2022, GCR Connect offers Genetic Counsellors with a space to discuss the unique issues that arise in the research landscape, provides links to practical resources, and creates a supportive research Genetic Counselling network. This initiative has been endorsed by the Human Genetics Society of Australasia and is supported by both Australian Genomics and the Australasian Society of Genetic Counsellors.