In order to do this, we need to ask our patients to fill out a very simple outcome measure at the beginning and end of an episode of treatment. We then put this information into the national database, all of which remains anonymous.
On our consent form we ask if you are happy to have your data used in this way, it is of course not compulsory and not all patients are included. However, if you’re happy to fill out the forms, your help would be very gratefully received!
If you would like to see some more information, then please follow the link below which takes you to a patient information sheet explaining the study in full. If you have any questions, please just ask one of us.
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