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Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians
OBJECTIVES: Parental consent for the participation of their neonate in neonatal research is influenced by the quality of the information delivered and the interaction between parents and investigators. Failure to provide important information may lead to difficulties in the decision making process o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999079/ https://www.ncbi.nlm.nih.gov/pubmed/29897934 http://dx.doi.org/10.1371/journal.pone.0198097 |
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author | Neyro, Virginia Elie, Valéry Thiele, Nicole Jacqz-Aigrain, Evelyne |
author_facet | Neyro, Virginia Elie, Valéry Thiele, Nicole Jacqz-Aigrain, Evelyne |
author_sort | Neyro, Virginia |
collection | PubMed |
description | OBJECTIVES: Parental consent for the participation of their neonate in neonatal research is influenced by the quality of the information delivered and the interaction between parents and investigators. Failure to provide important information may lead to difficulties in the decision making process of parents. This Delphi survey aims to establish a consensus between parent representatives of neonatal associations and healthcare professionals concerning the information deemed essential by both parties in order to improve the recruitment of neonates into clinical trials. METHOD: This study was conducted in Europe among parent representatives and healthcare professionals. In this 3-phase study, 96 items were defined by the Scientific Committee (CS), composed of 11 clinicians (from 8 countries) and 1 parent representative of the European network of neonatal associations. Then the Committee of Experts (CE) composed of 16 clinicians were matched by country with 16 national parent representatives and evaluated these items in two rounds. The importance of each item was evaluated by each member of the CE on a scale between 1 and 9 based on their personal experience. RESULTS: Fifty eight items reached the second and final level of consensus. In contrast to clinicians, parent representatives preferred to be informed about the study by the physician in charge of their child. They also favoured additional support during the informed consent process and stated that both parents need to agree and sign. CONCLUSION: The set of 58 items on which parents and clinicians reached consensus will be helpful to healthcare professionals seeking parental consent for the inclusion of a neonate in a clinical trial. Providing parents with information about the trial by the investigator in the presence of the patient’s neonatologist, developing closer contacts with parents and informing them of the available support by parents associations may be helpful for parents. |
format | Online Article Text |
id | pubmed-5999079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59990792018-06-21 Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians Neyro, Virginia Elie, Valéry Thiele, Nicole Jacqz-Aigrain, Evelyne PLoS One Research Article OBJECTIVES: Parental consent for the participation of their neonate in neonatal research is influenced by the quality of the information delivered and the interaction between parents and investigators. Failure to provide important information may lead to difficulties in the decision making process of parents. This Delphi survey aims to establish a consensus between parent representatives of neonatal associations and healthcare professionals concerning the information deemed essential by both parties in order to improve the recruitment of neonates into clinical trials. METHOD: This study was conducted in Europe among parent representatives and healthcare professionals. In this 3-phase study, 96 items were defined by the Scientific Committee (CS), composed of 11 clinicians (from 8 countries) and 1 parent representative of the European network of neonatal associations. Then the Committee of Experts (CE) composed of 16 clinicians were matched by country with 16 national parent representatives and evaluated these items in two rounds. The importance of each item was evaluated by each member of the CE on a scale between 1 and 9 based on their personal experience. RESULTS: Fifty eight items reached the second and final level of consensus. In contrast to clinicians, parent representatives preferred to be informed about the study by the physician in charge of their child. They also favoured additional support during the informed consent process and stated that both parents need to agree and sign. CONCLUSION: The set of 58 items on which parents and clinicians reached consensus will be helpful to healthcare professionals seeking parental consent for the inclusion of a neonate in a clinical trial. Providing parents with information about the trial by the investigator in the presence of the patient’s neonatologist, developing closer contacts with parents and informing them of the available support by parents associations may be helpful for parents. Public Library of Science 2018-06-13 /pmc/articles/PMC5999079/ /pubmed/29897934 http://dx.doi.org/10.1371/journal.pone.0198097 Text en © 2018 Neyro et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Neyro, Virginia Elie, Valéry Thiele, Nicole Jacqz-Aigrain, Evelyne Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians |
title | Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians |
title_full | Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians |
title_fullStr | Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians |
title_full_unstemmed | Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians |
title_short | Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians |
title_sort | clinical trials in neonates: how to optimise informed consent and decision making? a european delphi survey of parent representatives and clinicians |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999079/ https://www.ncbi.nlm.nih.gov/pubmed/29897934 http://dx.doi.org/10.1371/journal.pone.0198097 |
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