CONSENT OF CLINICAL RESEARCH PARTICIPANTS: FREE AND ENCOURAGED? (Atena Editora)

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MetadadosDescriçãoIdioma
Autor(es): dc.contributor.authorCastro, Talita Garcia do Nascimento de-
Autor(es): dc.contributor.authorMapelli, Lina Domênica-
Autor(es): dc.contributor.authorGozzo, Thais de Oliveira-
Data de aceite: dc.date.accessioned2022-03-17T14:33:12Z-
Data de disponibilização: dc.date.available2022-03-17T14:33:12Z-
Data de envio: dc.date.issued2022-03-15-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/700288-
Resumo: dc.description.abstractTo evaluate the consent process of clinical research participants. Method: descriptive study with prospective collection. Results: after the descriptive analysis of the data and comparison between the variables through univariate analyses, of the 70 participants who composed the sample, 83% were women; with a mean age of 46.7 years; 55.7% were white; 45.75% had a partner; 52.9% low schooling; 49.3% economically active. Of the participant, research and Free and Informed Consent Term: 35.7% were unaware of the type of study they participated in (Observational, Surgery, Medicine); information about the risks or discomforts that could be experienced while participating in the research was received by 51.4%, while 62.3% were informed of the benefits; 62.7% had no information on indemnities; 66.2% confirmed that they did not read the entire document before signing; about the form and content of the document, 86.8% of the participants reported that the ICF was easy to read, 62.2% found the document long, and 71.1% reported that the words in the document were easy to understand. Conclusion: it is pertinent to encourage national studies that assess perceptions of research participants regarding their rights, as well as the construction of instruments that allow this verification in the Brazilian population.pt_BR
Idioma: dc.language.isoenpt_BR
Palavras-chave: dc.subjectCLINICALpt_BR
Título: dc.titleCONSENT OF CLINICAL RESEARCH PARTICIPANTS: FREE AND ENCOURAGED? (Atena Editora)pt_BR
Tipo de arquivo: dc.typelivro digitalpt_BR
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