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Mind the gap? The platform trial as a working environment

BACKGROUND: Trials have become bigger and more complicated due to the complexity introduced by biomarker stratification, and the advent of multi-arm multi-stage trials, and umbrella and basket platform designs. The trials unit at University College London has been at the forefront of this work, with...

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Autores principales: Morrell, Liz, Hordern, Joshua, Brown, Louise, Sydes, Matthew R., Amos, Claire L., Kaplan, Richard S., Parmar, Mahesh K. B., Maughan, Timothy S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540560/
https://www.ncbi.nlm.nih.gov/pubmed/31138284
http://dx.doi.org/10.1186/s13063-019-3377-5
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author Morrell, Liz
Hordern, Joshua
Brown, Louise
Sydes, Matthew R.
Amos, Claire L.
Kaplan, Richard S.
Parmar, Mahesh K. B.
Maughan, Timothy S.
author_facet Morrell, Liz
Hordern, Joshua
Brown, Louise
Sydes, Matthew R.
Amos, Claire L.
Kaplan, Richard S.
Parmar, Mahesh K. B.
Maughan, Timothy S.
author_sort Morrell, Liz
collection PubMed
description BACKGROUND: Trials have become bigger and more complicated due to the complexity introduced by biomarker stratification, and the advent of multi-arm multi-stage trials, and umbrella and basket platform designs. The trials unit at University College London has been at the forefront of this work, with ground-breaking trials such as STAMPEDE and FOCUS4. The trial management and data management teams on these trials have summarised the operational challenges, to enable the broader clinical trials community to learn from their experiences. In a small-scale qualitative study, we examined the personal experience of individual researchers working on these trials. COMMENTARY: We found reports of high workloads, with potentially significant stress for individuals and with an impact on their career choices. We conclude that there was an initial underestimation of the work required and of the inherent, largely unanticipated, challenges. We discuss the importance of fully understanding these trials’ resource requirements, both for those writing grant applications and critically, for those with responsibility for deciding on funding. The working environment was characterised by three features: complexity, scale and heightened expectations. These features are highly attractive for professional development and engender high levels of loyalty and commitment. We observed a trade-off between these intrinsic rewards and the continuous demands of overlapping tasks, balancing a mix of routine and high-profile work, and the changing nature of pivotal roles. Such demands present challenges for colleague relationships, by enhancing the potential for competition and by disrupting the natural opportunities to pause, review and celebrate team achievements. In addition, molecular stratification in effect brings the patient into the trial office, as a specific individual, despite anonymisation, who is owed test results and a treatment decision. We discuss these observations with a view to interconnecting the need for compassion for patients with caring for the researchers engaged in the research ecosystem who are aiming to produce much hoped-for advances in medical science. CONCLUSIONS: There is a need for increased awareness of the challenge these studies place on those throughout the team delivering the study. Such considerations must influence leaders and funders, both in their initial budget considerations and throughout delivery.
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spelling pubmed-65405602019-06-03 Mind the gap? The platform trial as a working environment Morrell, Liz Hordern, Joshua Brown, Louise Sydes, Matthew R. Amos, Claire L. Kaplan, Richard S. Parmar, Mahesh K. B. Maughan, Timothy S. Trials Commentary BACKGROUND: Trials have become bigger and more complicated due to the complexity introduced by biomarker stratification, and the advent of multi-arm multi-stage trials, and umbrella and basket platform designs. The trials unit at University College London has been at the forefront of this work, with ground-breaking trials such as STAMPEDE and FOCUS4. The trial management and data management teams on these trials have summarised the operational challenges, to enable the broader clinical trials community to learn from their experiences. In a small-scale qualitative study, we examined the personal experience of individual researchers working on these trials. COMMENTARY: We found reports of high workloads, with potentially significant stress for individuals and with an impact on their career choices. We conclude that there was an initial underestimation of the work required and of the inherent, largely unanticipated, challenges. We discuss the importance of fully understanding these trials’ resource requirements, both for those writing grant applications and critically, for those with responsibility for deciding on funding. The working environment was characterised by three features: complexity, scale and heightened expectations. These features are highly attractive for professional development and engender high levels of loyalty and commitment. We observed a trade-off between these intrinsic rewards and the continuous demands of overlapping tasks, balancing a mix of routine and high-profile work, and the changing nature of pivotal roles. Such demands present challenges for colleague relationships, by enhancing the potential for competition and by disrupting the natural opportunities to pause, review and celebrate team achievements. In addition, molecular stratification in effect brings the patient into the trial office, as a specific individual, despite anonymisation, who is owed test results and a treatment decision. We discuss these observations with a view to interconnecting the need for compassion for patients with caring for the researchers engaged in the research ecosystem who are aiming to produce much hoped-for advances in medical science. CONCLUSIONS: There is a need for increased awareness of the challenge these studies place on those throughout the team delivering the study. Such considerations must influence leaders and funders, both in their initial budget considerations and throughout delivery. BioMed Central 2019-05-29 /pmc/articles/PMC6540560/ /pubmed/31138284 http://dx.doi.org/10.1186/s13063-019-3377-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Commentary
Morrell, Liz
Hordern, Joshua
Brown, Louise
Sydes, Matthew R.
Amos, Claire L.
Kaplan, Richard S.
Parmar, Mahesh K. B.
Maughan, Timothy S.
Mind the gap? The platform trial as a working environment
title Mind the gap? The platform trial as a working environment
title_full Mind the gap? The platform trial as a working environment
title_fullStr Mind the gap? The platform trial as a working environment
title_full_unstemmed Mind the gap? The platform trial as a working environment
title_short Mind the gap? The platform trial as a working environment
title_sort mind the gap? the platform trial as a working environment
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540560/
https://www.ncbi.nlm.nih.gov/pubmed/31138284
http://dx.doi.org/10.1186/s13063-019-3377-5
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