I’m working on a PhD project that aims to study the use of self-tracked health data, particularly (but not restricted to) those who may be managing long‐term (chronic) health conditions. The study specifically tries to understand how participants interpret and make use of this data both individually, and collaboratively, when shared with their doctors/clinicians. The objective is to develop design guidelines and frameworks that help integrate self-tracked data better into the chronic disease management process.
As a recent post suggested, doctors seem “uncooperative” in supporting QS. And there’s also the issue of the ‘scientific method in QS’ that was raised , which links to all this. Hope you can participate in the survey (as well as a follow-up interview), towards addressing some of these real-world challenges. The survey link - https://redcap.healthinformatics.unimelb.edu.au/surveys/?s=HXTPHM7TMM
Thanks in advance, for your time, support and interest