Cochrane invites 'citizen scientists' to identify and summarise randomised controlled trials

[Sasha]

I'd hoped that Cochrane's invitation to be a 'citizen scientist' was a bit exciting than this:

http://crowd.cochrane.org/index.html

But thought I'd mention it.

Are there ME/CFS RCTs missing from the database?

 

[Esther12]

There next conference is supposed to be all 'patient led':

http://www.evidentlycochrane.net/cochraneforall-tweetchat/

Wonder if there's any way we could use that to get them to actually listen to patients?

 

[Sasha]

I think that deserves its own separate thread, @Esther12.