Implementation of risk based monitoring into academic led clinical trials in Ireland

Show simple item record

dc.contributor.advisor Eustace, Joe en
dc.contributor.advisor Kearney, Patricia M. en
dc.contributor.advisor Shiely, Frances en
dc.contributor.advisor Clark, Mike en
dc.contributor.advisor Flanagan, Evelyn en
dc.contributor.author Hurley, Caroline
dc.date.accessioned 2019-05-22T12:29:02Z
dc.date.available 2019-05-22T12:29:02Z
dc.date.issued 2018
dc.date.submitted 2018
dc.identifier.citation Hurley, C. 2018. Implementation of risk based monitoring into academic led clinical trials in Ireland. PhD Thesis, University College Cork. en
dc.identifier.endpage 240 en
dc.identifier.uri http://hdl.handle.net/10468/7967
dc.description.abstract Introduction: In November 2016, the International Conference on Harmonsation (ICH) published a requirement for sponsors to develop a systematic, prioritised, risk-based approach to monitoring clinical trials. This process is more commonly known as Risk Based Monitoring (RBM). However, evidence suggested that a gold standard validated approach to RBM did not exist and it was unclear how sponsors would introduce RBM into their clinical trials units (CTUs). In 2014, Ireland, unlike countries such as Switzerland and the UK, did not have a national strategy to support the introduction of RBM into its publicly funded, academic-led CTUs. The absence of a national strategy and gold standard RBM approach meant it was not clear how RBM would be implemented in CTUs. Therefore, the overarching aim of this thesis was to develop, implement and evaluate a quality improvement intervention to support the introduction of RBM into academic-led clinical trials in Ireland. Methods: This thesis employed a multi-method research strategy directed by the Knowledge to Action (KTA) framework over four years from October 2014 to October 2018. The KTA framework is a conceptual framework to assist the translation of knowledge into sustainable, evidence-based interventions. This thesis used a range of research methods, implemented in four separate sequential phases, to address different components of the KTA framework which primarily involve knowledge creation and knowledge translations. The four phases first involved systematically reviewing the existing evidence of RBM methods. Then, in a mixed method study, I explored the attitudes, and perceived barriers and facilitators to the implementation of RBM in academic-led clinical trials in Ireland. Next, I did a document analysis study to examine the experience of monitoring in a clinical trial. Finally, I developed the quality improvement study by combining the results of the three earlier phases to identify the most appropriate quality improvement intervention to support RBM use in academic led clinical trials in Ireland. Results: The systematic review showed several tools exist to support the implementation of RBM. The mixed methods study showed a need for training and regulatory endorsed guidelines to support the implementation of RBM in academic-led clinical trials. The document analysis showed that on-site and centralised monitoring can be used simultaneously to fulfil ICH GCP’s seventeen monitoring requirements. The findings of these three studies were combined and a brief, face-to-face, interactive education workshop was identified as an effective way to encourage RBM tool usage among clinical researchers working in academic-led clinical trials in Ireland. Conclusion: Applying the KTA framework to empirical data has led to an intervention that is implementable in clinical practice and has the potential to positively change monitoring practices of clinical researchers. This thesis provides critical evidence on the complexities associated with implementing RBM in academic-led clinical trials. It provides practical recommendations to guide clinical researchers who wish to perform RBM. en
dc.format.mimetype application/pdf en
dc.language.iso en en
dc.publisher University College Cork en
dc.rights © 2018, Caroline Hurley. en
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/ en
dc.subject Risk based monitoring en
dc.subject Clinical trial en
dc.title Implementation of risk based monitoring into academic led clinical trials in Ireland en
dc.type Doctoral thesis en
dc.type.qualificationlevel Doctoral en
dc.type.qualificationname PhD en
dc.internal.availability Full text available en
dc.check.info Not applicable en
dc.description.version Accepted Version
dc.contributor.funder University College Cork en
dc.contributor.funder Health Research Board en
dc.description.status Not peer reviewed en
dc.internal.school Public Health en
dc.check.type No Embargo Required
dc.check.reason Not applicable en
dc.check.opt-out Not applicable en
dc.thesis.opt-out false
dc.check.embargoformat Embargo not applicable (If you have not submitted an e-thesis or do not want to request an embargo) en
ucc.workflow.supervisor j.eustace@ucc.ie
dc.internal.conferring Summer 2019 en
dc.internal.ricu HRB Clinical Research Facility at UCC en
dc.relation.project University College Cork (Strategic Research Fund) en
dc.relation.project Health Research Board (Trial Methodology Research Network) en


Files in this item

This item appears in the following Collection(s)

Show simple item record

© 2018, Caroline Hurley. Except where otherwise noted, this item's license is described as © 2018, Caroline Hurley.
This website uses cookies. By using this website, you consent to the use of cookies in accordance with the UCC Privacy and Cookies Statement. For more information about cookies and how you can disable them, visit our Privacy and Cookies statement