Register here if you want to access the forum and members only areas of this website. Click here for more information.
There are a number of resources available intended to support the implementation of outcome evaluation.
To find the measures CORC is currently recommending, click here. To find out more about published studies which describe or have used the measures, click here.
Databases and spreadsheets for use with these measures can be found on the Data collection page.
It is up to individual member services to decide on which database to use for storing and analysing data. CORC is not promoting any one type of service database or electronic patient record. Click here for more information on Data Collection
Each CORC Member can collect their data in whatever systems they have available. These range from Electronic Patient Records, the YouthinMind database and bespoke databases (or a combination of these!).
Click here to access and download the current databases.
CORC has developed a series of Information Sheets which aim to provide tips and advice on a variety of topics relating to outcomes. Click here for more information.
CORC provides a general presentation for members – the latest version can be downloaded here.
CORC Research Team are a resource in themselves and endeavour to support members by providing (yearly) site visits, telephone and email support and all the above resources.
Click here to find out what commercial databases other member services are using and what support is available.
Currently the CORC Central Team have been looking at the most helpful ways they can assist with the presentation of demographic data and have created a document entitled 'How to find population characteristics for your area' which helps services to make sense of the national statistics website.