Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era
Background: Currently, many initiatives are devoted to optimizing informed consent for participation in clinical research. Due to the digital transformation in health care, a shift toward electronic informed consent (eIC) has been fostered. However, empirical evidence on how to implement eIC in clin...
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doaj-c5c4e757d4c742448940816238f847452021-09-04T01:46:42ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602021-09-01910.3389/fped.2021.724431724431Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital EraEvelien De Sutter0Birte Coopmans1Femke Vanendert2Marc Dooms3Karel Allegaert4Karel Allegaert5Karel Allegaert6Pascal Borry7Isabelle Huys8Clinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, BelgiumClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, BelgiumClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, BelgiumClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, BelgiumClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, BelgiumDepartment of Development and Regeneration, KU Leuven, Leuven, BelgiumDepartment of Clinical Pharmacy, Erasmus MC, Rotterdam, NetherlandsCentre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, BelgiumClinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, BelgiumBackground: Currently, many initiatives are devoted to optimizing informed consent for participation in clinical research. Due to the digital transformation in health care, a shift toward electronic informed consent (eIC) has been fostered. However, empirical evidence on how to implement eIC in clinical research involving neonates is lacking.Methods: Semi-structured interviews were conducted with 31 health care professionals active in Belgium or the Netherlands. All health care professionals had experience in conducting clinical research involving neonates. Interviews were audio-recorded, transcribed and analyzed using the framework method.Results: Interviewees generally supported the use of eIC in clinical research involving neonates. For example, eIC could enable parents to receive study feedback via the eIC system. Requirements were expressed for parental involvement to decide on which feedback would be appropriate to return. Moreover, experts specialized in presenting information and designing electronic systems should be involved. Broad consensus among health care professionals indicates that the face-to-face-interaction between parents and the research team is vital to establish a relationship of trust. Therefore, it is necessary that the use of eIC runs alongside personal interactions with the parents. Concerns were raised about the accessibility of eIC to parents. For this reason, it was suggested that parents should always be given the possibility to read and sign a paper-based informed consent form or to use eIC.Conclusions: Health care professionals' views indicate that the use of eIC in clinical research with neonates may offer various opportunities. Further development and implementation will require a multi-stakeholder approach.https://www.frontiersin.org/articles/10.3389/fped.2021.724431/fullnewborninfanthealth care professionalqualitative researchclinical trialethics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Evelien De Sutter Birte Coopmans Femke Vanendert Marc Dooms Karel Allegaert Karel Allegaert Karel Allegaert Pascal Borry Isabelle Huys |
spellingShingle |
Evelien De Sutter Birte Coopmans Femke Vanendert Marc Dooms Karel Allegaert Karel Allegaert Karel Allegaert Pascal Borry Isabelle Huys Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era Frontiers in Pediatrics newborn infant health care professional qualitative research clinical trial ethics |
author_facet |
Evelien De Sutter Birte Coopmans Femke Vanendert Marc Dooms Karel Allegaert Karel Allegaert Karel Allegaert Pascal Borry Isabelle Huys |
author_sort |
Evelien De Sutter |
title |
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era |
title_short |
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era |
title_full |
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era |
title_fullStr |
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era |
title_full_unstemmed |
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era |
title_sort |
clinical research in neonates: redesigning the informed consent process in the digital era |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Pediatrics |
issn |
2296-2360 |
publishDate |
2021-09-01 |
description |
Background: Currently, many initiatives are devoted to optimizing informed consent for participation in clinical research. Due to the digital transformation in health care, a shift toward electronic informed consent (eIC) has been fostered. However, empirical evidence on how to implement eIC in clinical research involving neonates is lacking.Methods: Semi-structured interviews were conducted with 31 health care professionals active in Belgium or the Netherlands. All health care professionals had experience in conducting clinical research involving neonates. Interviews were audio-recorded, transcribed and analyzed using the framework method.Results: Interviewees generally supported the use of eIC in clinical research involving neonates. For example, eIC could enable parents to receive study feedback via the eIC system. Requirements were expressed for parental involvement to decide on which feedback would be appropriate to return. Moreover, experts specialized in presenting information and designing electronic systems should be involved. Broad consensus among health care professionals indicates that the face-to-face-interaction between parents and the research team is vital to establish a relationship of trust. Therefore, it is necessary that the use of eIC runs alongside personal interactions with the parents. Concerns were raised about the accessibility of eIC to parents. For this reason, it was suggested that parents should always be given the possibility to read and sign a paper-based informed consent form or to use eIC.Conclusions: Health care professionals' views indicate that the use of eIC in clinical research with neonates may offer various opportunities. Further development and implementation will require a multi-stakeholder approach. |
topic |
newborn infant health care professional qualitative research clinical trial ethics |
url |
https://www.frontiersin.org/articles/10.3389/fped.2021.724431/full |
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