“…Whilst what constitutes “fair” benefits was contested, there was broad agreement that benefits be defined in direct relation to burdens: as risks increase, so should the benefits [ 36 ]. Certain risk / benefit considerations were identified as requiring special attention in emergencies: - awareness of socio-political context [ 1 , 15 ] including safety considerations such as when gathering groups [ 21 ];
- strength of confidentiality and anonymity procedures, avoiding (inadvertent) disclosure, recognising the harm this may cause to individuals and communities [ 21 , 35 , 40 ];
- understanding the impact dissemination may have upon communities receiving aid and services [ 41 , 42 ];
- adequate responses to research participants’ discomfort or adverse reactions, including functional referral pathways for MHPSS care [ 14 , 18 , 26 , 29 , 31 , 32 , 35 , 43 , 44 ] determined by the level of risk that the research [ 45 ] or the participant’s situation presents [ 46 ];
- communication of risks and benefits in informed consent, identifying risks that matter to participants in/following a particular emergency [ 39 ].
- ensuring researcher self-care [ 14 , 31 ].
…”