PROP-OA

PROvision of braces for Patients with knee OsteoArthritis (PROP OA): a randomised controlled trial

UPDATED - 28 January 2022

(Search coding updated to SNOMED codes & New instructions.  Update to Pop-up Instructions to include SNOMED trigger code list)

NOTE FOR GP SITES: to avoid the potential of inadvertently identifying patients without knee pain, please use the SNOMED version of the search shared below.  If you have used the READ coded version of the search, but have not contacted patients yet, please re-start the patient ID process using the SNOMED search.

A multi-centre, primary care, randomised, parallel-group, superiority trial (with internal pilot) to evaluate the effectiveness of bracing in the management of symptomatic knee osteoarthritis: the PROP OA trial.  AIM(S) OF THE RESEARCH: To show whether wearing a knee brace provides more relief for people with painful osteoarthritis of the knee than just having best primary care (education, advice and exercise), and whether this is good value for money for the NHS.

HI History

EMIS - Search and pop-up developed by CRN West Midlands ROST (updated 28 January 2022)

SystmOne  - Search and pop-up designed by Dr Gareth Forbes on behalf of LCRN North East & North Cumbria

Files available for download for the following delivery LCRNs:

West Midlands / North East & North Cumbria / Greater Manchester / North West Coast

PLEASE NOTE - Search files do not include exclusion codes linked to Data Dissent


If other LCRNs would like access to these files, please email rost.crnwestmidlands@nihr.ac.uk

EMIS Web Resources


SystmOne

See instruction document linked below for details on how to access the PROP-OA resources for SystmnOne

Disclaimer:

Please note the resources provided are designed to assist with the identification of potentially suitable patients and to appropriately code these patient if required.


These resources have been developed based on the criteria provided by the relevant study team and whilst every effort has been made to make them universally implementable they rely on read codes and the data stored in the individual practice's clinical system. These resources are intended to assist with identification but should be used in conjunction with clinical oversight and a clear understanding of the study parameters. 


While we endeavour to keep the information, tools and resources provided up to date and correct, we make no representations or warranties of any kind, express or implied, about the completeness, accuracy, reliability, suitability or availability with respect to the tools provided for any purpose. Any reliance you place on such information is therefore strictly at your own risk.


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