I came across this (open-access) article today in the BMJ (British Medical Journal) from August 2017:
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research http://www.bmj.com/content/358/bmj.j3453
Although patient/public involvement in research is not the same as participatory design, I thought this theoretical work might be of interest to design researchers, for instance people studying the impact of involving users and stakeholders in design processes. A lot of health care research is a about developing "things" (interventions for improving health, design of information systems, new ways of providing services and care, etc) so there is much potential for overlap between our fields.
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