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Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Dr
Ivan
Koychev
ivan.koychev@psych.ox.ac.uk
Dr
Ivan
Koychev
ivan.koychev@psych.ox.ac.uk
Dishaa
Sinha
dishaa.sinha@psych.ox.ac.uk
Hussein
Mehmet
hussein.mehmet@psych.ox.ac.uk
Aurelija
Burbaite
aurelija.burbaite@psych.ox.ac.uk
Organic, including symptomatic, mental disorders
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
This study is designed to determine the feasibility and acceptability of collecting and analysing blood samples as well as cognitive data relevant to dementia risk from three sources of participants in the Oxfordshire region (an online research register, cognitive disorders clinic and GP practices) to inform a larger study. Blood samples from 1000 participants will be taken on two occasions 12 months apart at the John Radcliffe Hospital. During the study visit, the participant will also complete a questionnaire to provide feedback on the study visit as well as the invitation process; they will also be asked to complete cognitive tests online at 6 monthly intervals (3 tests in total).
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Observational type: Cohort study;
You can take part if:
You may not be able to take part if:
• Have difficult venous access; • Lack of access to PC or tablet connected to the internet; • Not fluent in English.
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Dr
Ivan
Koychev
ivan.koychev@psych.ox.ac.uk
Dishaa
Sinha
dishaa.sinha@psych.ox.ac.uk
Dr
Ivan
Koychev
ivan.koychev@psych.ox.ac.uk
Aurelija
Burbaite
aurelija.burbaite@psych.ox.ac.uk
Hussein
Mehmet
hussein.mehmet@psych.ox.ac.uk
The study is sponsored by University of Oxford and funded by Medical Research Council (MRC) .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 54471
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
