Abstract

The need for improved ethics guidelines in a changing research landscape

Highlights

  • The term non-medical refers to the application of social science and humanities methodologies and instruments relating to human participants outside of medical, clinical or therapeutic settings

  • Based on the foregoing, it is appropriate to ask whether national and global guidelines on research ethics involving human participants are fit for purpose, because (1) these guidelines have been developed mainly for medical rather than non-medical research and (2) they do not speak to the specific methods of data collection and analysis, and the nature of risk and vulnerability, used in many areas of the social sciences and humanities

  • The important point is that new research instruments and participant groups available to social science researchers may give rise to new types of ethical issues related to confidentiality, anonymity, privacy and consent that are not covered by existing guidelines

Read more

Summary

The need for improved ethics guidelines in a changing research landscape

Ethics guidelines for conducting research involving human subjects have been informed by practices and procedures developed for, and with reference to, medical research.[1,2] This indication is clear from international guidelines on research ethics practices, including the Belmont Report[3] and the Declaration of Helsinki[4]. There are limitations as to the extent to which they can be applied to research that involves human subjects but in non-medical and non-therapeutic settings (here termed human participants) In this context, the term non-medical refers to the application of social science and humanities methodologies and instruments relating to human participants outside of medical, clinical or therapeutic settings. The term non-medical refers to the application of social science and humanities methodologies and instruments relating to human participants outside of medical, clinical or therapeutic settings This type of research includes data collection using qualitative and interactive methods, such as interviews, questionnaires, workshops, focus groups and ethnographic observations.

Research ethics context in South Africa
Future directions in human research ethics
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.