Ethics in Qualitative Research
Main Article Content
Abstract
Ethical considerations are essential to ensure that any research project takes place responsibly, respecting the rights and well-being of participants and maintaining scientific integrity. This article presents the safeguards of qualitative research, emphasizing bioethical principles and the handling of personal data. Researchers must implement rigorous measures to ensure confidentiality. That includes obtaining informed consent from participants before collecting personal data, using secure methods for data storage and transmission, and ensuring that data protection measures prevent data from being used in a way that could identify identity. When interviews are the collection method, they should consider the implications of audio recordings (voice recognition) and video recordings (image protection). The collected data may be sensitive and reveal delicate information about individuals, so verbatims must be anonymized.
Downloads
Article Details
Section

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
How to Cite
References
Organización Mundial de la Salud, Consejo de Organizaciones Internacionales de Ciencias Médicas (CIOMS). Pautas éticas internacionales para la investigación relacionada con la salud con seres humanos [Internet]. Ginebra: CIOMS; 2017 [citado 2023 ago 22]. Disponible en: https://cioms.ch/wp-content/uploads/2017/12/CIOMS-EthicalGuideline_SP_INTERIOR-FINAL.pdf.
Masic I. The importance of proper citation of references in biomedical articles. Acta Inform Med. 2013;21(3):148-155. https://doi.org/10.5455/aim.2013.21.148-155. DOI: https://doi.org/10.5455/aim.2013.21.148-155
Varkey B. Principles of clinical ethics and their application to practice. Med Princ Pract. 2021;30(1):17-28. https://doi.org/10.1159/000509119. DOI: https://doi.org/10.1159/000509119
Im D, Pyo J, Lee H, et al. Qualitative research in healthcare: data analysis. J Prev Med Public Health. 2023;56(2):100-110. https://doi.org/10.3961/jpmph.22.471. DOI: https://doi.org/10.3961/jpmph.22.471
Argentina. Ministerio de Salud. Resolución 1480/2011: Guía para investigaciones con seres humanos [Internet]. Buenos Aires: el Ministerio; 2011 [citada 2023 ago 22]. Disponible en: https://www.argentina.gob.ar/normativa/nacional/resoluci%C3%B3n-1480-2011-187206/actualizacion.
Argentina. Honorable Congreso de la Nación. Ley 26.529: Derechos del paciente en su relación con los profesionales e instituciones de la salud [Internet]. Buenos Aires: el Congreso; 2009 [citado 2023 ago 22]. Disponible en: https://www.argentina.gob.ar/normativa/nacional/ley-26529-160432/texto.
Graham GN. Why your ZIP code matters more than your genetic code: promoting healthy outcomes from mother to child. Breastfeed Med. 2016;11:396-397. https://doi.org/10.1089/bfm.2016.0113. DOI: https://doi.org/10.1089/bfm.2016.0113
El Emam K, Buckeridge D, Tamblyn R, et al. The re-identification risk of Canadians from longitudinal demographics. BMC Med Inform Decis Mak. 2011;11:46. https://doi.org/10.1186/1472-6947-11-46. DOI: https://doi.org/10.1186/1472-6947-11-46
Guía práctica para la protección de datos personales en salud [Internet]. Buenos Aires: Fundar; 2023 [citado 2023 ago 22]. Disponible en: https://fund.ar/publicacion/guia-proteger-datos-en-salud/.
Argentina. Código civil y comercial. Artículo 53: derecho a la imagen [Internet]. Buenos Aires: Argentina. Ministerio de Justicia; 2014 [citado 2023 ago 22]. Disponible en: https://servicios.infoleg.gob.ar/infolegInternet/anexos/235000-239999/235975/texact.htm#6.
Artal R, Rubenfeld S. Ethical issues in research. Best Pract Res Clin Obstet Gynaecol. 2017;43:107-114. https://doi.org/10.1016/j.bpobgyn.2016.12.006. DOI: https://doi.org/10.1016/j.bpobgyn.2016.12.006
De Sutter E, Zaçe D, Boccia S, et al. Implementation of electronic informed consent in biomedical research and stakeholders' perspectives: systematic review. J Med Internet Res. 2020;22(10):e19129. https://doi.org/10.2196/19129. DOI: https://doi.org/10.2196/19129