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A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology

BACKGROUND: In pediatric oncology, many oncologists invite their own patients to participate in research. Inclusion within a dependent relationship is considered to potentially compromise voluntariness of consent. Currently, it is unknown to what extent those involved in pediatric oncology experienc...

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Autores principales: Dekking, Sara A. S., van der Graaf, Rieke, Schouten-van Meeteren, Antoinette Y. N., Kars, Marijke C., van Delden, Johannes J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819802/
https://www.ncbi.nlm.nih.gov/pubmed/26755349
http://dx.doi.org/10.1007/s40272-015-0158-9
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author Dekking, Sara A. S.
van der Graaf, Rieke
Schouten-van Meeteren, Antoinette Y. N.
Kars, Marijke C.
van Delden, Johannes J. M.
author_facet Dekking, Sara A. S.
van der Graaf, Rieke
Schouten-van Meeteren, Antoinette Y. N.
Kars, Marijke C.
van Delden, Johannes J. M.
author_sort Dekking, Sara A. S.
collection PubMed
description BACKGROUND: In pediatric oncology, many oncologists invite their own patients to participate in research. Inclusion within a dependent relationship is considered to potentially compromise voluntariness of consent. Currently, it is unknown to what extent those involved in pediatric oncology experience the dependent relationship as a threat to voluntary informed consent, and what they see as safeguards to protect voluntary informed consent within a dependent relationship. AIM: We performed a qualitative study among key actors in pediatric oncology to explore their experiences with the dependent relationship and voluntary informed consent. METHODS: We conducted three focus groups and 25 semi-structured, in-depth interviews with pediatric oncologists, research coordinators, Research Ethics Committee members, parents of children with cancer, and adolescents with cancer. RESULTS: Professionals regarded the dependent relationship both as a potential threat to and as a positive influence on voluntary decision making. Parents and adolescents did not feel as though dependency upon the oncologist influenced their decisions. They valued the involvement of their own physician in the informed consent process. The professionals suggested three strategies to protect voluntariness: emphasizing voluntariness; empowering families; involvement of an independent person. CONCLUSIONS: Although the dependent relationship between pediatric oncologists, patients and parents may be problematic for voluntary informed consent, this is not necessarily the case. Moreover, the involvement of treating physicians may even have a positive impact on the informed consent process. Although we studied pediatric oncology, our results may also apply to many other fields of pediatric medicine where research and care are combined, for example, pediatric rheumatology, neurology and nephrology. Clinical trials in these fields are inevitably often designed, initiated and conducted by medical specialists closely involved in patient care. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40272-015-0158-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-48198022016-04-11 A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology Dekking, Sara A. S. van der Graaf, Rieke Schouten-van Meeteren, Antoinette Y. N. Kars, Marijke C. van Delden, Johannes J. M. Paediatr Drugs Original Research Article BACKGROUND: In pediatric oncology, many oncologists invite their own patients to participate in research. Inclusion within a dependent relationship is considered to potentially compromise voluntariness of consent. Currently, it is unknown to what extent those involved in pediatric oncology experience the dependent relationship as a threat to voluntary informed consent, and what they see as safeguards to protect voluntary informed consent within a dependent relationship. AIM: We performed a qualitative study among key actors in pediatric oncology to explore their experiences with the dependent relationship and voluntary informed consent. METHODS: We conducted three focus groups and 25 semi-structured, in-depth interviews with pediatric oncologists, research coordinators, Research Ethics Committee members, parents of children with cancer, and adolescents with cancer. RESULTS: Professionals regarded the dependent relationship both as a potential threat to and as a positive influence on voluntary decision making. Parents and adolescents did not feel as though dependency upon the oncologist influenced their decisions. They valued the involvement of their own physician in the informed consent process. The professionals suggested three strategies to protect voluntariness: emphasizing voluntariness; empowering families; involvement of an independent person. CONCLUSIONS: Although the dependent relationship between pediatric oncologists, patients and parents may be problematic for voluntary informed consent, this is not necessarily the case. Moreover, the involvement of treating physicians may even have a positive impact on the informed consent process. Although we studied pediatric oncology, our results may also apply to many other fields of pediatric medicine where research and care are combined, for example, pediatric rheumatology, neurology and nephrology. Clinical trials in these fields are inevitably often designed, initiated and conducted by medical specialists closely involved in patient care. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40272-015-0158-9) contains supplementary material, which is available to authorized users. Springer International Publishing 2016-01-11 2016 /pmc/articles/PMC4819802/ /pubmed/26755349 http://dx.doi.org/10.1007/s40272-015-0158-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial 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.
spellingShingle Original Research Article
Dekking, Sara A. S.
van der Graaf, Rieke
Schouten-van Meeteren, Antoinette Y. N.
Kars, Marijke C.
van Delden, Johannes J. M.
A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology
title A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology
title_full A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology
title_fullStr A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology
title_full_unstemmed A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology
title_short A Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology
title_sort qualitative study into dependent relationships and voluntary informed consent for research in pediatric oncology
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819802/
https://www.ncbi.nlm.nih.gov/pubmed/26755349
http://dx.doi.org/10.1007/s40272-015-0158-9
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