#hcsm – June 28, 2015
- Most patient self-tracked data isn’t going into their health record. Should it? If so, how? Or, why not?
- how might we make it easier for pts to donate their data to research? Could SM be used for informed consent? Why/not?
- as a research participant, do you want to know outcome of a study? How can SM be used to communicate research outcomes?
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