Cochrane UK Consumer Champions: another step towards better patient and public involvement

Cochrane UK has launched the Cochrane UK Consumer Champions initiative and we are inviting applications from people who would like to join us. The consumer champions role will involve advocating for evidence-based health care and Cochrane amongst organisations and patient groups in the UK. Cochrane uses the term ‘consumer’ to represent patients, carers and family members with experience of a healthcare condition. Emma Doble, Patient and Consumer Co-ordinator, and Marta Santos, Programme Support Officer at Cochrane UK, who are leading this initiative, explain more in this blog.

Emma was diagnosed with Type 1 Diabetes at the age of 4. After struggling to accept and manage her diabetes growing up, she started to set up a number of peer support initiatives for other young people. She then started to get involved in Public and Patient Involvement (PPI) groups for diabetes services and research projects. She also has a keen interest in getting more young people involved in PPI.

Emma shares with us how she got involved in Cochrane and what inspired the Cochrane UK Consumer Champions initiative:

I initially heard of Cochrane when I saw a tweet inviting patient advocates to apply for an award to join the Colloquium (Cochrane’s annual conference) in Edinburgh in 2018. I started to look at the Cochrane websites and was amazed at the huge amount of resources which were aimed at supporting and informing patients about their health conditions. Attending the Colloquium, I began to get a sense of the varied patient and public involvement Cochrane advocated for, but I also noticed that there were several patient groups who weren’t represented.

Over the next few months, I tried to get more involved in Cochrane and explored how I could help more diverse groups of patients get involved in the organisation. I also began to wonder why I had not heard of Cochrane as a patient advocate despite a history of PPI in the organisation. I questioned whether the connection between patient communities and Cochrane could be better established to help bridge the gap.

The idea for consumer champions came from this desire to better involve more diverse groups of patients and the public, whilst also bridging the gap between Cochrane and consumers. The consumer champions role has been developed with the aim of identifying and supporting new patients and groups to get involved in Cochrane. The champions will also share Cochrane’s resources within their own networks to allow a wider group of patients to know about Cochrane’s work and how they can use the resources.

You can apply for the role by sending the application form (attached below) to Marta Santos on marta.santos@cochrane.nhs.uk. Applicants must be based in the UK and meet the eligibility criteria as described in the person specification document attached.

If would like to learn more about what being involved Cochrane UK Consumer Champion means, please look at the support booklet that we created to guide Consumer Champions or aspiring Consumer Champions through their journey.

We will continue to write more blogs to keep you updated on the project’s progress.

Should you have any questions, please send us an email to general@cochrane.nhs.uk.

Join in the conversation on Twitter with @CochraneUK  @emmajdoble  leave a comment on the blog. Please note, we cannot give medical advice and we will not publish comments that link to commercial sites or appear to endorse commercial products.



Cochrane UK Consumer Champions: another step towards better patient and public involvement by Emma Doble

is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International

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