#hcsm – June 28, 2015


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

Don’t forget – if you’d like to submit a topic for a future #hcsm chat, you’re welcome to! Read the details on the different ways to submit a topic for a #hcsm chat. Also, if you missed the chat, or want to add additional thoughts & feedback to the above discussion topics, leave a comment & keep the discussion going!



  1. No trackbacks yet.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

%d bloggers like this: