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Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial

BACKGROUND: Delphi surveys are commonly used to prioritise critical outcomes in core outcome set (COS) development. This trial aims to compare a three-round (Multi-Round) Delphi (MRD) with a Real-Time Delphi (RTD) in the prioritisation of outcomes for inclusion in a COS for neonatal encephalopathy t...

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Autores principales: Quirke, Fiona A., Battin, Malcolm R., Bernard, Caitlin, Biesty, Linda, Bloomfield, Frank H., Daly, Mandy, Finucane, Elaine, Haas, David M., Healy, Patricia, Hurley, Tim, Koskei, Sarah, Meher, Shireen, Molloy, Eleanor J., Niaz, Maira, Bhraonáin, Elaine Ní, Okaronon, Christabell Omukagah, Tabassum, Farhana, Walker, Karen, Webbe, James R. H., Parkes, Matthew J., Kirkham, Jamie J., Devane, Declan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354951/
https://www.ncbi.nlm.nih.gov/pubmed/37468987
http://dx.doi.org/10.1186/s13063-023-07388-9
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author Quirke, Fiona A.
Battin, Malcolm R.
Bernard, Caitlin
Biesty, Linda
Bloomfield, Frank H.
Daly, Mandy
Finucane, Elaine
Haas, David M.
Healy, Patricia
Hurley, Tim
Koskei, Sarah
Meher, Shireen
Molloy, Eleanor J.
Niaz, Maira
Bhraonáin, Elaine Ní
Okaronon, Christabell Omukagah
Tabassum, Farhana
Walker, Karen
Webbe, James R. H.
Parkes, Matthew J.
Kirkham, Jamie J.
Devane, Declan
author_facet Quirke, Fiona A.
Battin, Malcolm R.
Bernard, Caitlin
Biesty, Linda
Bloomfield, Frank H.
Daly, Mandy
Finucane, Elaine
Haas, David M.
Healy, Patricia
Hurley, Tim
Koskei, Sarah
Meher, Shireen
Molloy, Eleanor J.
Niaz, Maira
Bhraonáin, Elaine Ní
Okaronon, Christabell Omukagah
Tabassum, Farhana
Walker, Karen
Webbe, James R. H.
Parkes, Matthew J.
Kirkham, Jamie J.
Devane, Declan
author_sort Quirke, Fiona A.
collection PubMed
description BACKGROUND: Delphi surveys are commonly used to prioritise critical outcomes in core outcome set (COS) development. This trial aims to compare a three-round (Multi-Round) Delphi (MRD) with a Real-Time Delphi (RTD) in the prioritisation of outcomes for inclusion in a COS for neonatal encephalopathy treatments and explore whether ‘feedback’, ‘iteration’, and ‘initial condition’ effects may occur in the two survey methods. METHODS: We recruited 269 participants (parents/caregivers, healthcare providers and researchers/academics) of which 222 were randomised to either the MRD or the RTD. We investigated the outcomes prioritised in each survey and the ‘feedback’, ‘iteration’, and ‘initial condition’ effects to identify differences between the two survey methods. RESULTS: In the RTD, n = 92 participants (83%) fully completed the survey. In the MRD, n = 60 participants (54%) completed all three rounds. Of the 92 outcomes presented, 26 (28%) were prioritised differently between the RTD and MRD. Significantly fewer participants amended their scores when shown stakeholder responses in the RTD compared to the MRD (‘feedback effect’). The ‘iteration effect’ analysis found most experts appeared satisfied with their initial ratings in the RTD and did not amend their scores following stakeholder response feedback. Where they did amend their scores, ratings were amended substantially, suggesting greater convergence. Variance in scores reduced with subsequent rounds of the MRD (‘iteration effect’). Whilst most participants did not change their initial scores in the RTD, of those that did, later recruits tended to align their final score more closely to the group mean final score than earlier recruits (an ‘initial condition’ effect). CONCLUSION: The feedback effect differed between the two Delphi methods but the magnitude of this difference was small and likely due to the large number of observations rather than because of a meaningfully large difference. It did not appear to be advantageous to require participants to engage in three rounds of a survey due to the low change in scores. Larger drop-out through successive rounds in the MRD, together with a lesser convergence of scores and longer time to completion, indicate considerable benefits of the RTD approach. TRIAL REGISTRATION: NCT04471103. Registered on 14 July 2020. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-023-07388-9.
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spelling pubmed-103549512023-07-20 Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial Quirke, Fiona A. Battin, Malcolm R. Bernard, Caitlin Biesty, Linda Bloomfield, Frank H. Daly, Mandy Finucane, Elaine Haas, David M. Healy, Patricia Hurley, Tim Koskei, Sarah Meher, Shireen Molloy, Eleanor J. Niaz, Maira Bhraonáin, Elaine Ní Okaronon, Christabell Omukagah Tabassum, Farhana Walker, Karen Webbe, James R. H. Parkes, Matthew J. Kirkham, Jamie J. Devane, Declan Trials Research BACKGROUND: Delphi surveys are commonly used to prioritise critical outcomes in core outcome set (COS) development. This trial aims to compare a three-round (Multi-Round) Delphi (MRD) with a Real-Time Delphi (RTD) in the prioritisation of outcomes for inclusion in a COS for neonatal encephalopathy treatments and explore whether ‘feedback’, ‘iteration’, and ‘initial condition’ effects may occur in the two survey methods. METHODS: We recruited 269 participants (parents/caregivers, healthcare providers and researchers/academics) of which 222 were randomised to either the MRD or the RTD. We investigated the outcomes prioritised in each survey and the ‘feedback’, ‘iteration’, and ‘initial condition’ effects to identify differences between the two survey methods. RESULTS: In the RTD, n = 92 participants (83%) fully completed the survey. In the MRD, n = 60 participants (54%) completed all three rounds. Of the 92 outcomes presented, 26 (28%) were prioritised differently between the RTD and MRD. Significantly fewer participants amended their scores when shown stakeholder responses in the RTD compared to the MRD (‘feedback effect’). The ‘iteration effect’ analysis found most experts appeared satisfied with their initial ratings in the RTD and did not amend their scores following stakeholder response feedback. Where they did amend their scores, ratings were amended substantially, suggesting greater convergence. Variance in scores reduced with subsequent rounds of the MRD (‘iteration effect’). Whilst most participants did not change their initial scores in the RTD, of those that did, later recruits tended to align their final score more closely to the group mean final score than earlier recruits (an ‘initial condition’ effect). CONCLUSION: The feedback effect differed between the two Delphi methods but the magnitude of this difference was small and likely due to the large number of observations rather than because of a meaningfully large difference. It did not appear to be advantageous to require participants to engage in three rounds of a survey due to the low change in scores. Larger drop-out through successive rounds in the MRD, together with a lesser convergence of scores and longer time to completion, indicate considerable benefits of the RTD approach. TRIAL REGISTRATION: NCT04471103. Registered on 14 July 2020. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-023-07388-9. BioMed Central 2023-07-19 /pmc/articles/PMC10354951/ /pubmed/37468987 http://dx.doi.org/10.1186/s13063-023-07388-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Quirke, Fiona A.
Battin, Malcolm R.
Bernard, Caitlin
Biesty, Linda
Bloomfield, Frank H.
Daly, Mandy
Finucane, Elaine
Haas, David M.
Healy, Patricia
Hurley, Tim
Koskei, Sarah
Meher, Shireen
Molloy, Eleanor J.
Niaz, Maira
Bhraonáin, Elaine Ní
Okaronon, Christabell Omukagah
Tabassum, Farhana
Walker, Karen
Webbe, James R. H.
Parkes, Matthew J.
Kirkham, Jamie J.
Devane, Declan
Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial
title Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial
title_full Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial
title_fullStr Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial
title_full_unstemmed Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial
title_short Multi-Round versus Real-Time Delphi survey approach for achieving consensus in the COHESION core outcome set: a randomised trial
title_sort multi-round versus real-time delphi survey approach for achieving consensus in the cohesion core outcome set: a randomised trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354951/
https://www.ncbi.nlm.nih.gov/pubmed/37468987
http://dx.doi.org/10.1186/s13063-023-07388-9
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