Professional Documents
Culture Documents
The following are elements of research ethics that require specific attention in the
context of the COVID-19 pandemic:
All studies should comply with the disaster emergency laws, rules, and guidelines
of the country where the research is conducted.
Applicants and researchers will be required to adhere to all preventive measures
as advised by the World Health Organization and national guidance.
No research activities should be undertaken if they impede emergency
responses.
Safety considerations for research participants, as well as researchers, are
paramount in health emergency and pandemic contexts. Research design needs
to have clear protocols of risk assessment and mitigation strategies to ensure
protection from risk of infection and to mitigate other health risks, including
potential mental health impacts on research participants and researchers.
Remote interaction and conducting online or internet-based research are likely to
be part of the research design with COVID-19 restrictions in place. These
present specific ethical concerns regarding privacy, transparency, confidentiality,
and security. Specific measures must be devised, implemented, and documented
to:
o ensure transparency during recruitment;
o take necessary steps for data security and ensure that data are not used
for subsequent non-research purposes.
o offer participants the opportunity to modify their data; and
o offer participants the opportunity to withdraw from the research and retract
their data;
o obtain informed and knowledgeable consent and ensure that consent is
obtained on an ongoing basis;
o use secure communication protocols and platforms;
o consider the expectations of participants about privacy;
Note that research methodologies should not be modified if doing so would compromise
the ethical standard of the research.
Who sets the research agenda? Is research designed and defined at the local level,
and how are priorities set? How are local perspectives reconciled with global agenda-
setting, and how is research embedded in local knowledge ecosystems? Are there risks
and bias in terms of research that is concentrated in and about easily accessible
locations that might exclude less accessible areas and populations?
Who is the research for? How can research projects balance the benefits for the
funder, the researcher, and research participants, and how can research findings be
used to improve the well-being of research participants and populations? Funders may
have a need for research to inform interventions, but they need to balance the risk of
exacerbating vulnerabilities of targeted groups. Projects need to engage with a wide
variety of research partners in addition to various local groups to avoid the convenience
of narrow engagement.