Informed consent in scientific research: what should we know?

Detalhes bibliográficos
Autor(a) principal: Moreira, José
Data de Publicação: 2022
Outros Autores: Miguel, Susana, Frade, Ana
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/10400.14/48152
Resumo: Informed consent is a pillar of the research and imperative in an ethical dimension. Given its inherent principles in an increasingly rigorous and responsible investigation, this process is complex, making it challenging to reflect on its validity from an ethical and deontological perspective. We are witnessing the fast development of knowledge in biomedicine intrinsic to unprecedented technological innovation, with increased complex studies and repercussions on consent. Among them, the simplification and validation of information to be transmitted to the participant, the possibility to extend the period for clarifying possible doubts, the use of support tools, and optimization of the communication by researchers. Overly technical terms, difficult interpretation of the information, little explanation, different cultures, and sociopolitical ideologies affect the researchers’ differentiation. Given the several legal dimensions of consent, the relevance of free and informed exercise of the rights provided by law for scientific development in health was demonstrated. In addition to an opportunity for effective communication, informed consent must be based on a trust relationship between the investigator and the participant, based on ethical principles. These are essential to the development of rational and robust research, somehow guiding the work to be carried out by researchers, including the principles of beneficence, non-maleficence, justice, autonomy, and precaution. Therefore, the participant assumes an active role in the success or suspension of the investigation, and the investigators are responsible for respecting the informed and free decision.
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spelling Informed consent in scientific research: what should we know?Consentimento informado em pesquisa científica: o que devemos saber?BioethicsInformed consentClinical ethicsDeontologyBioéticaConsentimento informadoÉtica clínicaDeontologiaInformed consent is a pillar of the research and imperative in an ethical dimension. Given its inherent principles in an increasingly rigorous and responsible investigation, this process is complex, making it challenging to reflect on its validity from an ethical and deontological perspective. We are witnessing the fast development of knowledge in biomedicine intrinsic to unprecedented technological innovation, with increased complex studies and repercussions on consent. Among them, the simplification and validation of information to be transmitted to the participant, the possibility to extend the period for clarifying possible doubts, the use of support tools, and optimization of the communication by researchers. Overly technical terms, difficult interpretation of the information, little explanation, different cultures, and sociopolitical ideologies affect the researchers’ differentiation. Given the several legal dimensions of consent, the relevance of free and informed exercise of the rights provided by law for scientific development in health was demonstrated. In addition to an opportunity for effective communication, informed consent must be based on a trust relationship between the investigator and the participant, based on ethical principles. These are essential to the development of rational and robust research, somehow guiding the work to be carried out by researchers, including the principles of beneficence, non-maleficence, justice, autonomy, and precaution. Therefore, the participant assumes an active role in the success or suspension of the investigation, and the investigators are responsible for respecting the informed and free decision.VeritatiMoreira, JoséMiguel, SusanaFrade, Ana2025-02-19T09:19:06Z2022-07-012022-07-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.14/48152eng1647-055910.34632/cadernosdesaude.2022.11469info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-13T10:43:01Zoai:repositorio.ucp.pt:10400.14/48152Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T01:37:14.626739Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Informed consent in scientific research: what should we know?
Consentimento informado em pesquisa científica: o que devemos saber?
title Informed consent in scientific research: what should we know?
spellingShingle Informed consent in scientific research: what should we know?
Moreira, José
Bioethics
Informed consent
Clinical ethics
Deontology
Bioética
Consentimento informado
Ética clínica
Deontologia
title_short Informed consent in scientific research: what should we know?
title_full Informed consent in scientific research: what should we know?
title_fullStr Informed consent in scientific research: what should we know?
title_full_unstemmed Informed consent in scientific research: what should we know?
title_sort Informed consent in scientific research: what should we know?
author Moreira, José
author_facet Moreira, José
Miguel, Susana
Frade, Ana
author_role author
author2 Miguel, Susana
Frade, Ana
author2_role author
author
dc.contributor.none.fl_str_mv Veritati
dc.contributor.author.fl_str_mv Moreira, José
Miguel, Susana
Frade, Ana
dc.subject.por.fl_str_mv Bioethics
Informed consent
Clinical ethics
Deontology
Bioética
Consentimento informado
Ética clínica
Deontologia
topic Bioethics
Informed consent
Clinical ethics
Deontology
Bioética
Consentimento informado
Ética clínica
Deontologia
description Informed consent is a pillar of the research and imperative in an ethical dimension. Given its inherent principles in an increasingly rigorous and responsible investigation, this process is complex, making it challenging to reflect on its validity from an ethical and deontological perspective. We are witnessing the fast development of knowledge in biomedicine intrinsic to unprecedented technological innovation, with increased complex studies and repercussions on consent. Among them, the simplification and validation of information to be transmitted to the participant, the possibility to extend the period for clarifying possible doubts, the use of support tools, and optimization of the communication by researchers. Overly technical terms, difficult interpretation of the information, little explanation, different cultures, and sociopolitical ideologies affect the researchers’ differentiation. Given the several legal dimensions of consent, the relevance of free and informed exercise of the rights provided by law for scientific development in health was demonstrated. In addition to an opportunity for effective communication, informed consent must be based on a trust relationship between the investigator and the participant, based on ethical principles. These are essential to the development of rational and robust research, somehow guiding the work to be carried out by researchers, including the principles of beneficence, non-maleficence, justice, autonomy, and precaution. Therefore, the participant assumes an active role in the success or suspension of the investigation, and the investigators are responsible for respecting the informed and free decision.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-01
2022-07-01T00:00:00Z
2025-02-19T09:19:06Z
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dc.relation.none.fl_str_mv 1647-0559
10.34632/cadernosdesaude.2022.11469
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