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New national service to support #LynchSyndrome patients needing #colonoscopy - many thanks for the support of the ⁦@BritSocGastro⁩ - designed to provide better access to care for patients during the #Covid19 pandemic & recovery phase

The future of UK medical research is at risk, including pioneering projects that I work on for @CRUK_Policy.

@hammersmithandy as my MP, please sign this letter to show your support and help us continue to make progress for patients


Britain’s Cancer Crisis
@bbcpanorama : Monday 6th July 7.30pm.
Tune in and join the conversation using the hashtag #britainscancercrisis @BBCNews #youmebigc

How to get feedback about research - a lovely short video sharing one novel and engaging method from Kelly Gleason
@Imperial_PERC @imperialCR_UK @ECMC_UK @PersonalisePLY @ImperialBRC

The CSPRG wishing a fond farewell to Iain, our wonderful Data Analyst who is sadly leaving us today☹️ Iain will be greatly missed by the team but we would like to wish him all the best of luck for the future.

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Public involvement

We believe that public and patient involvement (PPI) in the design and conduct of trials and studies improves the quality of the research that we undertake. The value of the patient perspective and experience is integral to any research activity that affects patients. PPI gives the patients and members of the public the opportunity to have their say in the way our studies are conducted and help suggest important changes to benefit future and on-going research.

There are lots of ways you can get involved in our research, including joining one of our trial steering groups as a patient representative, joining in discussions on new research ideas, helping design study questionnaires and reviewing patient information sheets.

We are interested in hearing from you, whether you are a patient affected by bowel cancer, or are caring for someone with bowel cancer. If you have any suggestions or comments, or want to be a patient representative for our research please contact us.

For researchers

Data used in CSPRG research was collected subject to the informed consent of the participants and / or under section 251 support. Access to the individual level anonymised data will only be granted in line with the relevant informed consent form or section 251 support, subject to approval by the appropriate research ethics committee, Health Research Authority (HRA) and HRA Confidentiality Advisory Group (HRA-CAG) as required, under a formal data sharing agreement.

To discuss a request for data please contact the CSPRG by completing the contact form with the following information: the proposed study objectives, the data you require and timelines for completion of the research.