Research Taking Part

Taking part in research

Banbury Cross Health Centre is involved in medical research and from time to time you may be approached to take part. Taking part in research is voluntary: you can freely accept or decline, and this will not affect the care that you receive in any way. Even if you agree to take part, you can still withdraw at any time, without having to provide justification. Withdrawing from a study will NOT affect the care we provide for you.

All research projects carried out at Banbury Cross Health Centre have been thoroughly checked and approved by the relevant health authorities & ethical committees ensuring it is appropriate and safe to perform.

You will always receive clear information about what taking part in a research study would involve and will have the opportunity to ask questions and obtain further details about a study. All projects are fully compliant with all UK laws (incl. GDPR).

You may receive a text message or a letter in the post offering you the opportunity to take part in a study (the letter will include some information about the project).
Your doctor or nurse may also discuss research opportunities during your usual appointment.
You may also be approached by a member of the study team in the waiting area; be assured that this person and their activity will have been approved by the practice.

What you will be asked to do as part of the research will vary from study to study. The Patient Information Sheet for each project will detail what is expected of you. The study team is also there to answer all questions you may have.

Things you may want to know

Participation in research is entirely voluntary and you have the right to say ‘No’. Nobody will put pressure on you to take part in research if you do not wish to. You do not have to give us a reason if you decide not to take part.
Your care and your relationship with your doctor or nurse will not be affected in any way if you decide not to take part in a research study.
You will always receive clear information about what taking part in a research study would involve. The practice will usually provide you with a patient information sheet; then, if you agree to take part, the study team will explain the study to you in more detail and you will have the opportunity to ask questions about it.
Nobody from outside this practice will be given your contact details or have access to your medical records without your prior consent. If you do agree to take part in a study, you will be asked to sign a consent form – this will clearly state which parts of your notes (if any) may be looked at for the purposes of the research.
You will not be asked to take part in a large number of studies. Most researchers are very specific about the criteria that people need to meet in order to enter their study. Usually this means that only a relatively small number of patients at the practice will be suitable for any one study.

Anonymous data sharing for research

This practice is also participating in two national database projects which collect anonymised electronic medical records collected from GP surgeries throughout the UK. Through the electronic clinical system we use to record medical notes, a completely anonymous (i.e. no identifiable patient details are shared at all) extract is taken which is used for medical research. This clinical data is then catalogued and provides continuous monitoring of infection and disease around the UK.

What if I don’t want to get involved in research?

We recognise that some people may not want to receive information about research studies by post or text message. If you do not want to be contacted about research studies that we may run at the practice in the future, please let us know. If you change your mind at a later date, you can still opt back in at any time.

To opt out of participating in any research studies visit the NHS Your Data Matters website to set your preferences

National Institute for Health Research logo