Open Access Ethics Resources for Researchers
By Dr. Helen Kara
Independent researcher Dr. Helen Kara recently completed an important new book: Research Ethics in the Real World. She also co-edited a special issue on "New Directions in Qualitative Research Ethics" for the March 2017 International Journal of Social Research Methodology. She generously agreed to share this collection of open access ethics resources with Methodspace readers. You can find more of her writings about ethics, conducting research, writing and getting published, on her blog. Find more posts about ethics on Methodspace here
Are you grappling with research ethics? If so, fear not, for there are numerous free resources online to help you. Here are some examples.
Ethical codes and guidelines
There are loads of ethical codes and guidelines online. For example, some countries have national codes of research ethics, such as the Australian Code for the Responsible Conduct of Research or the Canadian Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans. This was developed in partnership between the Canadian Institutes of Health Research, the Natural Sciences and Engineering Research Council of Canada, and the Social Sciences and Humanities Research Council of Canada. There are also codes of research ethics produced by Indigenous peoples who wish their own ethical principles to be followed by any researchers who wish to work with them. Examples of these include Te Ara Tika, Guidelines for Māori Research Ethics, from New Zealand, and the San Code of Research Ethics from South Africa. Then there are professional and disciplinary codes of research ethics. Examples include the UK-based Market Research Society’s Code of Conduct, and the Code of Ethics of the Australian Association for Research in Education
.There must be a huge number of these kinds of codes and guidelines worldwide. They are not all the same, and the careful reader can find places where one code or guideline may contradict another. This is because of cultural (in its widest sense) differences in ideas of what is ethical. Nevertheless, they can be useful to read for learning, ideas, or of course specific contextual information.
Applying to a research ethics committee
If you have to apply to a research ethics committee for formal ethical approval, you might find it useful to see some other researchers’ successful application forms. You can find examples of these on The Research Ethics Application Database (TREAD), originally set up by Martin Tolich at Otago University in New Zealand and now hosted by The Global Health Network and the Social Research Association. This database holds copies of successful ethics applications from around the world which you can search and use for inspiration and learning. Applications are anonymised, though the researcher(s) must be named. Researchers often submit accompanying documents, such as consent forms and participant information sheets, which can be very useful to look through for ideas. The database managers are keen to add more applications, to help make formal ethical approval processes more accessible and less onerous. If you have an application you could submit, there is information on the websiteabout how to share it via the database.
General guidance
The Research Ethics Guidebook is intended to provide general guidance for social scientists, but may also be useful for people from other fields. The Guidebook is supported by the UK’s Economic and Social Research Council, with the Researcher Development Initiative of the National Centre for Research Methods, and London University’s Institute of Education. Like TREAD, the Research Ethics Guidebook holds useful information about applying for formal ethical approval. However, it also covers other areas such as ethics in research design, conducting research, reporting, and dissemination. The Guidebook is ideal for reference at the start of a project, and also during research as unforeseen ethical dilemmas occur.
Ethics training
There are two free online courses in research ethics which are primarily geared towards health researchers and so focus heavily on participant wellbeing. Both have been through peer review and other quality assurance processes, and both offer certificates to students who complete the course successfully with a score of 80% or more. One is called Research Ethics Online Training and is adapted from an e-learning course and resource package designed and produced by the World Health Organisation. It contains 14 individual modules, plus resources in the form of a glossary, a “resource library” (aka bibliography), some case studies, examples of ethics guidelines, videos on research ethics, and links to other ethics websites. The second is Essential Elements of Ethics is adapted from an ethics tool kit created to support researchers at Harvard University in America. This course contains 11 modules, plus resources including a workbook and checklist of points to consider, and a discussion forum though this is not very active. Free research ethics modules with a wider perspective are offered by Duke University in America. These cover topics such as cultural awareness and humility, ethical photography, power and privilege, and working with children. They are delivered through videos with transcripts also available.
Online research
For internet-based research, the Association of Internet Researchers has some useful resources free for download. The British Psychological Society offers Ethics Guidelines for Internet-mediated Research. The South East European Network for Professionalization of Media has produced Social Media Research: A Guide to Ethics.
Visual research
The International Visual Sociology Association has produced a Code of Research Ethics and Guidelines covering visual research.
Ethics of research publication
The Committee on Publication Ethics has a whole range of downloadable resources covering how to detect, prevent and handle misconduct, responsible publication standards for editors and authors, ethical guidelines for peer reviewers, and much more. This list of resources is by no means exhaustive. There are loads more out there. It would be a huge task to identify them all. These are the ones I have found particularly useful.
Informed consent is the term given to the agreement between researcher and participant. In this post Janet Salmons offers suggestions about the intersections of the Internet communications, ethics and participants.