Hello all,
I was wondering if anyone who has been involved in co-research, especially with people labelled as having learning difficulties or other 'vulnerable' groups, have experienced the need (from funding bodies or institutions) to gain informed consent from the potential co-researchers?
People participating in research clearly need to give consent and as researchers we are morally obliged to ensure that consent is informed in all cases, but does this in anyone else's experience apply to any co-researchers working in participatory or inclusive research where the co-researchers are not respondents but going to be interviewing disabled and non-disabled respondents from whom informed consent would be sought?
I've not come across any discussion of this issue in the literature, but obviously I might have missed it.
Kind regards,
Liz Ellis
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