Welcome! The OpenClinica Participate Documentation contains all the information you’ll need to get your study subjects really participating in your study by allowing them to use mobile devices to respond directly into OpenClinica forms. This allows for more accurate responses and means that clinical research coordinators can spend more time with study participants, typically meaning a higher level of subject compliance.

With Openclinica Participate, you have total control over when forms are available for each subject, and the data is captured in real time. This means there is no option for subjects to pre-fill or back-fill forms. The underlying audit trail offers evidence that the subjects completed the forms in the timeframe dictated by the protocol.

OpenClinica Participate (OCP) works with electronic case report forms (eCRFs) designed in OpenClinica. For information on designing OpenClinica eCRFs, see Create and Modify Case Report Forms. To enable your Study for use with OCP, see the topics below.

As always, as an open source community we love your feedback and contributions. 

cleaner data capture so study coordinators can spend more time with their study participants and potentially enjoy higher patient compliance. – See more at: http://social.eyeforpharma.com/digital/using-electronic-patient-reported-outcomes-epro-first-time-lessons-learned#sthash.rjjxm9qX.dpuf
cleaner data capture so study coordinators can spend more time with their study participants and potentially enjoy higher patient compliance. – See more at: http://social.eyeforpharma.com/digital/using-electronic-patient-reported-outcomes-epro-first-time-lessons-learned#sthash.rjjxm9qX.dpuf
 cleaner data capture so study coordinators can spend more time with 
their study participants and potentially enjoy higher patient 
compliance.  - See more at: 
http://social.eyeforpharma.com/digital/using-electronic-patient-reported-outcomes-epro-first-time-lessons-learned#sthash.rjjxm9qX.dpuf
cleaner data capture so study coordinators can spend more time with their study participants and potentially enjoy higher patient compliance. – See more at: http://social.eyeforpharma.com/digital/using-electronic-patient-reported-outcomes-epro-first-time-lessons-learned#sthash.rjjxm9qX.dpuf
cleaner data capture so study coordinators can spend more time with their study participants and potentially enjoy higher patient compliance. – See more at: http://social.eyeforpharma.com/digital/using-electronic-patient-reported-outcomes-epro-first-time-lessons-learned#sthash.rjjxm9qX.dpuf
cleaner data capture so study coordinators can spend more time with their study participants and potentially enjoy higher patient compliance. – See more at: http://social.eyeforpharma.com/digital/using-electronic-patient-reported-outcomes-epro-first-time-lessons-learned#sthash.rjjxm9qX.dpuf
cleaner data capture so study coordinators can spend more time with their study participants and potentially enjoy higher patient compliance. – See more at: http://social.eyeforpharma.com/digital/using-electronic-patient-reported-outcomes-epro-first-time-lessons-learned#sthash.rjjxm9qX.dpuf