We’ve just finished day 2 of the workshop, and I’m pretty sure the facilitator thinks I’m the most annoying person in the world. What?! I’m enthusiastic!
I’m really enjoying the workshop, but am a bit concerned that we haven’t once spoken about the ethics around research communication. We’ve discussed in depth the use of social media, but ethical considerations have not been given the same consideration.
From my experience, once you’ve developed a research proposal you send it to an ethics committee who assess whether you have sufficiently engaged with the ethical implications of your research and will provide for your participants’ needs. By, for example, providing them with an outline of the research and your contact details, and the details of support networks and care providers if you are talking to vulnerable people or asking personal questions.
While, to my knowledge, research communication is not subjected to the same degree of scrutiny, as researchers this is definitely something we should be thinking about. The most effective way to communicate your research may be to use an image of a participant, but is that ethical? Perhaps it may be to use the moral panics around women and children, #sex and #moderndayslavery, but is it ethical to indulge that panic even momentarily and even if it gets people to read your research? We’re being told to communicate our research as much as possible, but every study has its limitations, and those limitations are seldom acknowledged in our dissemination where we focus on the findings and evidence – because that’s what people/policy makers want – but surely that’s problematic?
But perhaps I’m being too difficult, maybe all of these things are ok. There’s so much terrible information and bad evidence out there, if you have to appeal to people’s love of panic or breeze past your study’s limitations what’s the harm really? At least people are reading your work?