Ethics in Qualitative Research

Main Article Content

María F. Grande Ratti
Delfina Murature
Agustín Sánchez Del Roscio
Salomé Frei
Sonia E. Benitez

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

Download data is not yet available.

Article Details

Section

Notes on statistics and research

How to Cite

1.
Grande Ratti MF, Murature D, Sánchez Del Roscio A, Frei S, Benitez SE. Ethics in Qualitative Research. Rev Hosp Ital B.Aires [Internet]. 2024 Mar. 29 [cited 2026 Apr. 27];44(1):e0000295. Available from: https://ojs.hospitalitaliano.org.ar/index.php/revistahi/article/view/295

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

Most read articles by the same author(s)

<< < 1 2