I recently co-authored an article on research ethics for the journal Transgender Health. It’s based on an extensive review of literature on the topic, and written by an international team of scholars and health practitioners with extensive experience of conducting research in this field.
Transgender Health is an open access journal, so the article is freely available for anyone to read and share.
I’ve copied the abstract out below: please click on the title for full access.
The purpose of this review is to create a set of provisional criteria for Institutional Review Boards (IRBs) to refer to when assessing the ethical orientation of transgender health research proposals. We began by searching for literature on this topic using databases and the reference lists of key articles, resulting in a preliminary set of criteria. We then collaborated to develop the following nine guidelines:
(1) Whenever possible, research should be grounded, from inception to dissemination, in a meaningful collaboration with community stakeholders;
(2) language and framing of transgender health research should be non-stigmatizing;
(3) research should be disseminated back to the community;
(4) the diversity of the transgender and gender diverse (TGGD) community should be accurately reflected and sensitively reflected;
(5) informed consent must be meaningful, without coercion or undue influence;
(6) the protection of participant confidentiality should be paramount;
(7) alternative consent procedures should be considered for TGGD minors;
(8) research should align with current professional standards that refute conversion, reorientation, or reparative therapy; and
(9) IRBs should guard against the temptation to avoid, limit, or delay research on this subject.