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Published in: Trials 1/2022

Open Access 01-12-2022 | Methodology

What is the purpose of clinical trial monitoring?

Authors: Sharon B. Love, Victoria Yorke-Edwards, Elizabeth Ward, Rebecca Haydock, Katie Keen, Katie Biggs, Gosala Gopalakrishnan, Lucy Marsh, Lydia O’Sullivan, Lisa Fox, Estelle Payerne, Kerenza Hood, Garry Meakin

Published in: Trials | Issue 1/2022

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Abstract

Background

The sources of information on clinical trial monitoring do not give information in an accessible language and do not give detailed guidance. In order to enable communication and to build clinical trial monitoring tools on a strong easily communicated foundation, we identified the need to define monitoring in accessible language.

Methods

In a three-step process, the material from sources that describe clinical trial monitoring were synthesised into principles of monitoring. A poll regarding their applicability was run at a UK national academic clinical trials monitoring meeting.

Results

The process derived 5 key principles of monitoring: keeping participants safe and respecting their rights, having data we can trust, making sure the trial is being run as it was meant to be, improving the way the trial is run and preventing problems before they happen.

Conclusion

From the many sources mentioning monitoring of clinical trials, the purpose of monitoring can be summarised simply as 5 principles. These principles, given in accessible language, should form a firm basis for discussion of monitoring of clinical trials.
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Literature
Metadata
Title
What is the purpose of clinical trial monitoring?
Authors
Sharon B. Love
Victoria Yorke-Edwards
Elizabeth Ward
Rebecca Haydock
Katie Keen
Katie Biggs
Gosala Gopalakrishnan
Lucy Marsh
Lydia O’Sullivan
Lisa Fox
Estelle Payerne
Kerenza Hood
Garry Meakin
Publication date
01-12-2022
Publisher
BioMed Central
Published in
Trials / Issue 1/2022
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/s13063-022-06763-2

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