Following initial discussions with Outcomes Managers at NOA member trusts WWL and RJAH, this meeting will explore the creation of an NOA working group dedicated to Outcomes.
Outcomes data collection can mean different things to different people, ranging from PROMs data collection to national registries submission, to local data collection initiatives. The process needs clinical support and guidance, but the administrative support cannot be underestimated. Many decisions regarding data collection and registries are taken nationally with little consultation from Providers.
Full information can be found in the Members Area here. (All staff from NOA Member Trusts can access the members area of the website- you will need to have registered for the Members Only Area to gain access).
If you are interested or have any comments please email firstname.lastname@example.org.