Table 2.
Themes | Sub-themes |
---|---|
Rapidly evolving research ethics landscape |
Risk to benefit analysis as a moving target Placebo use in ongoing vaccine research Standard of care Post-trial access Social value |
Extreme vulnerability of research participants |
Individual and population vulnerability COVID-19 stigmatisation and prejudice Therapeutic misconception |
Unique challenges to informed consent |
Impact of fear and isolation on individual autonomy Challenges ‘on the ground’ Divergent views on consent waivers |
Challenges to community engagement during COVID-19 |
RECs own role in community engagement The ‘who, when and how’ of community engagement during a pandemic |
Overlapping research ethics and public health equity issues |
Inequitable burden of research Equity in research agendas Inequities in access |