Virtual consent and the use of electronic informed consent form in clinical research in Brazil

Detalhes bibliográficos
Autor(a) principal: Silva,Juliana Carvalho Rocha Alves da
Data de Publicação: 2021
Outros Autores: Capucho,Helaine Carneiro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista da Associação Médica Brasileira (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302021001201570
Resumo: SUMMARY OBJECTIVE: In view of the need to apply term free and informed consent (IC) in clinical research involving humans, in accordance with the Brazilian ethical standards (CNS Resolution No. 466/2012), it is necessary to assess whether this practice is being effective and can be improved. The aim of this study was to evaluate the use of the IC in electronic format (e-IC), regarding its feasibility and suitability, as a complement to the written/physical consent form. METHODS: Quantitative-qualitative research with a questionnaire instrument. RESULTS: Greater retention of information and fewer wrong answers were observed after the application of the e-IC. CONCLUSIONS: The use of e-IC is of great value to research participants in Brazil.
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spelling Virtual consent and the use of electronic informed consent form in clinical research in BrazilClinical trials as topicInformed consentEthics committeesResearchSUMMARY OBJECTIVE: In view of the need to apply term free and informed consent (IC) in clinical research involving humans, in accordance with the Brazilian ethical standards (CNS Resolution No. 466/2012), it is necessary to assess whether this practice is being effective and can be improved. The aim of this study was to evaluate the use of the IC in electronic format (e-IC), regarding its feasibility and suitability, as a complement to the written/physical consent form. METHODS: Quantitative-qualitative research with a questionnaire instrument. RESULTS: Greater retention of information and fewer wrong answers were observed after the application of the e-IC. CONCLUSIONS: The use of e-IC is of great value to research participants in Brazil.Associação Médica Brasileira2021-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302021001201570Revista da Associação Médica Brasileira v.67 n.11 2021reponame:Revista da Associação Médica Brasileira (Online)instname:Associação Médica Brasileira (AMB)instacron:AMB10.1590/1806-9282.20210621info:eu-repo/semantics/openAccessSilva,Juliana Carvalho Rocha Alves daCapucho,Helaine Carneiroeng2021-12-10T00:00:00Zoai:scielo:S0104-42302021001201570Revistahttps://ramb.amb.org.br/ultimas-edicoes/#https://old.scielo.br/oai/scielo-oai.php||ramb@amb.org.br1806-92820104-4230opendoar:2021-12-10T00:00Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)false
dc.title.none.fl_str_mv Virtual consent and the use of electronic informed consent form in clinical research in Brazil
title Virtual consent and the use of electronic informed consent form in clinical research in Brazil
spellingShingle Virtual consent and the use of electronic informed consent form in clinical research in Brazil
Silva,Juliana Carvalho Rocha Alves da
Clinical trials as topic
Informed consent
Ethics committees
Research
title_short Virtual consent and the use of electronic informed consent form in clinical research in Brazil
title_full Virtual consent and the use of electronic informed consent form in clinical research in Brazil
title_fullStr Virtual consent and the use of electronic informed consent form in clinical research in Brazil
title_full_unstemmed Virtual consent and the use of electronic informed consent form in clinical research in Brazil
title_sort Virtual consent and the use of electronic informed consent form in clinical research in Brazil
author Silva,Juliana Carvalho Rocha Alves da
author_facet Silva,Juliana Carvalho Rocha Alves da
Capucho,Helaine Carneiro
author_role author
author2 Capucho,Helaine Carneiro
author2_role author
dc.contributor.author.fl_str_mv Silva,Juliana Carvalho Rocha Alves da
Capucho,Helaine Carneiro
dc.subject.por.fl_str_mv Clinical trials as topic
Informed consent
Ethics committees
Research
topic Clinical trials as topic
Informed consent
Ethics committees
Research
description SUMMARY OBJECTIVE: In view of the need to apply term free and informed consent (IC) in clinical research involving humans, in accordance with the Brazilian ethical standards (CNS Resolution No. 466/2012), it is necessary to assess whether this practice is being effective and can be improved. The aim of this study was to evaluate the use of the IC in electronic format (e-IC), regarding its feasibility and suitability, as a complement to the written/physical consent form. METHODS: Quantitative-qualitative research with a questionnaire instrument. RESULTS: Greater retention of information and fewer wrong answers were observed after the application of the e-IC. CONCLUSIONS: The use of e-IC is of great value to research participants in Brazil.
publishDate 2021
dc.date.none.fl_str_mv 2021-11-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302021001201570
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302021001201570
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1806-9282.20210621
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Associação Médica Brasileira
publisher.none.fl_str_mv Associação Médica Brasileira
dc.source.none.fl_str_mv Revista da Associação Médica Brasileira v.67 n.11 2021
reponame:Revista da Associação Médica Brasileira (Online)
instname:Associação Médica Brasileira (AMB)
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collection Revista da Associação Médica Brasileira (Online)
repository.name.fl_str_mv Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)
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