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Digital tools in the informed consent process: a systematic review

BACKGROUND: Providing understandable information to patients is necessary to achieve the aims of the Informed Consent process: respecting and promoting patients’ autonomy and protecting patients from harm. In recent decades, new, primarily digital technologies have been used to apply and test innova...

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Autores principales: Gesualdo, Francesco, Daverio, Margherita, Palazzani, Laura, Dimitriou, Dimitris, Diez-Domingo, Javier, Fons-Martinez, Jaime, Jackson, Sally, Vignally, Pascal, Rizzo, Caterina, Tozzi, Alberto Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913441/
https://www.ncbi.nlm.nih.gov/pubmed/33639926
http://dx.doi.org/10.1186/s12910-021-00585-8
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author Gesualdo, Francesco
Daverio, Margherita
Palazzani, Laura
Dimitriou, Dimitris
Diez-Domingo, Javier
Fons-Martinez, Jaime
Jackson, Sally
Vignally, Pascal
Rizzo, Caterina
Tozzi, Alberto Eugenio
author_facet Gesualdo, Francesco
Daverio, Margherita
Palazzani, Laura
Dimitriou, Dimitris
Diez-Domingo, Javier
Fons-Martinez, Jaime
Jackson, Sally
Vignally, Pascal
Rizzo, Caterina
Tozzi, Alberto Eugenio
author_sort Gesualdo, Francesco
collection PubMed
description BACKGROUND: Providing understandable information to patients is necessary to achieve the aims of the Informed Consent process: respecting and promoting patients’ autonomy and protecting patients from harm. In recent decades, new, primarily digital technologies have been used to apply and test innovative formats of Informed Consent. We conducted a systematic review to explore the impact of using digital tools for Informed Consent in both clinical research and in clinical practice. Understanding, satisfaction and participation were compared for digital tools versus the non-digital Informed Consent process. METHODS: We searched for studies on available electronic databases, including Pubmed, EMBASE, and Cochrane. Studies were identified using specific Mesh-terms/keywords. We included studies, published from January 2012 to October 2020, that focused on the use of digital Informed Consent tools for clinical research, or clinical procedures. Digital interventions were defined as interventions that used multimedia or audio–video to provide information to patients. We classified the interventions into 3 different categories: video only, non-interactive multimedia, and interactive multimedia. RESULTS: Our search yielded 19,579 publications. After title and abstract screening 100 studies were retained for full-text analysis, of which 73 publications were included. Studies examined interactive multimedia (29/73), non-interactive multimedia (13/73), and videos (31/73), and most (34/38) studies were conducted on adults. Innovations in consent were tested for clinical/surgical procedures (26/38) and clinical research (12/38). For research IC, 21 outcomes were explored, with a positive effect on at least one of the studied outcomes being observed in 8/12 studies. For clinical/surgical procedures 49 outcomes were explored, and 21/26 studies reported a positive effect on at least one of the studied outcomes. CONCLUSIONS: Digital technologies for informed consent were not found to negatively affect any of the outcomes, and overall, multimedia tools seem desirable. Multimedia tools indicated a higher impact than videos only. Presence of a researcher may potentially enhance efficacy of different outcomes in research IC processes. Studies were heterogeneous in design, making evaluation of impact challenging. Robust study design including standardization is needed to conclusively assess impact.
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spelling pubmed-79134412021-03-02 Digital tools in the informed consent process: a systematic review Gesualdo, Francesco Daverio, Margherita Palazzani, Laura Dimitriou, Dimitris Diez-Domingo, Javier Fons-Martinez, Jaime Jackson, Sally Vignally, Pascal Rizzo, Caterina Tozzi, Alberto Eugenio BMC Med Ethics Research Article BACKGROUND: Providing understandable information to patients is necessary to achieve the aims of the Informed Consent process: respecting and promoting patients’ autonomy and protecting patients from harm. In recent decades, new, primarily digital technologies have been used to apply and test innovative formats of Informed Consent. We conducted a systematic review to explore the impact of using digital tools for Informed Consent in both clinical research and in clinical practice. Understanding, satisfaction and participation were compared for digital tools versus the non-digital Informed Consent process. METHODS: We searched for studies on available electronic databases, including Pubmed, EMBASE, and Cochrane. Studies were identified using specific Mesh-terms/keywords. We included studies, published from January 2012 to October 2020, that focused on the use of digital Informed Consent tools for clinical research, or clinical procedures. Digital interventions were defined as interventions that used multimedia or audio–video to provide information to patients. We classified the interventions into 3 different categories: video only, non-interactive multimedia, and interactive multimedia. RESULTS: Our search yielded 19,579 publications. After title and abstract screening 100 studies were retained for full-text analysis, of which 73 publications were included. Studies examined interactive multimedia (29/73), non-interactive multimedia (13/73), and videos (31/73), and most (34/38) studies were conducted on adults. Innovations in consent were tested for clinical/surgical procedures (26/38) and clinical research (12/38). For research IC, 21 outcomes were explored, with a positive effect on at least one of the studied outcomes being observed in 8/12 studies. For clinical/surgical procedures 49 outcomes were explored, and 21/26 studies reported a positive effect on at least one of the studied outcomes. CONCLUSIONS: Digital technologies for informed consent were not found to negatively affect any of the outcomes, and overall, multimedia tools seem desirable. Multimedia tools indicated a higher impact than videos only. Presence of a researcher may potentially enhance efficacy of different outcomes in research IC processes. Studies were heterogeneous in design, making evaluation of impact challenging. Robust study design including standardization is needed to conclusively assess impact. BioMed Central 2021-02-27 /pmc/articles/PMC7913441/ /pubmed/33639926 http://dx.doi.org/10.1186/s12910-021-00585-8 Text en © The Author(s) 2021 Open AccessThis 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/. 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 in a credit line to the data.
spellingShingle Research Article
Gesualdo, Francesco
Daverio, Margherita
Palazzani, Laura
Dimitriou, Dimitris
Diez-Domingo, Javier
Fons-Martinez, Jaime
Jackson, Sally
Vignally, Pascal
Rizzo, Caterina
Tozzi, Alberto Eugenio
Digital tools in the informed consent process: a systematic review
title Digital tools in the informed consent process: a systematic review
title_full Digital tools in the informed consent process: a systematic review
title_fullStr Digital tools in the informed consent process: a systematic review
title_full_unstemmed Digital tools in the informed consent process: a systematic review
title_short Digital tools in the informed consent process: a systematic review
title_sort digital tools in the informed consent process: a systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913441/
https://www.ncbi.nlm.nih.gov/pubmed/33639926
http://dx.doi.org/10.1186/s12910-021-00585-8
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