Angela Okune Annotations

How is consent described? Moralized? Are any "best practices" denoted?

Tuesday, January 28, 2020 - 7:07pm

AO: Some may view my uploading of these informed consent forms as simply another push towards an increased "audit culture" within the university (Strathern 1997) and greater politics of accountability (Shore 2008). I grappled with the implications of uploading these document but came to the conclusion that in the case of this project, these artifacts that seemed to be nothing more than university bureaucratic paperwork were in fact important data points for the project.

How did expressed desires from the interviews align or diverge from the practical decisions to share or not as made explicit in the consent form?

How legible was the formal consent form to diverse research participants or did it in fact further obfuscate important considerations when determining the risks or benefits of sharing?

In this way, I found that archiving this material was not simply to "save" or "preserve" it for an audit but rather to provide the grounds for further questions and deeper inquiry of the research object.

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How is being anonymized or named in research described? Moralized?

Tuesday, January 28, 2020 - 7:05pm

AO. Despite stating their desire to be anonymous, participant #KPKMU09 wrote out their whole name in a legible format on the consent form. (I had given verbal directions to those who wished to be anonymous not to write in their names and stated that I would write in a participant number instead afterwards). Ideally, this form should have been redesigned so as not to ask for names if one wishes to be anonymous. But as it was the officially approved IRB form, this example illustrates some of the cracks where formal mechanisms for protection may not be sufficient. It would not be hard to imagine how a larger sample size and less careful attention to explicit/implict patient desires and individual/collective risks might lead to a bulk uploading of such consent forms and increased exposure to individual and collective risks. Thus, taking the practices as I attempted in this project as "best practice" and scaling them up in other projects may not in fact be advisable nor desirable. I hope this example helps reveal the entanglements caught up in concepts like Open Data and how such "experiments" within the ethnographic endeavor (asking participants for their desired level of sharing, uploading and sharing materials including consent forms) should be seen as emergent forms rather than fixed targets or clear criteria to be achieved within careful consideration.

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