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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.
Brandy
Coote
brandycooteconsulting@outlook.com
Dr
Vanessa
Raymont
vanessa.raymont@psych.ox.ac.uk
Hannah
Rome-Hall
hannah.rome-hall@psych.ox.ac.uk
Hannah
Rome-Hall
hannah.rome-hall@psych.ox.ac.uk
Brandy
Coote
brandycooteconsulting@outlook.com
Organic, including symptomatic, mental disordersSymptoms and signs involving cognition, perception, emotional state and behaviour
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.
A dementia diagnosis is usually made from speaking with patients and families,memory testing,and
brain scans. While these methods are effective in identifying whether someone has dementia,they are
not reliable when it comes to the cause of the condition or how it may progress in future.
Blood tests are a promising way to improve the diagnosis of dementia. But the research so far had
participants who do not reflect real-world patient populations (for example in terms of their ethnicity or
having other common illnesses).
Here,we aim to assess the usefulness of blood-based tests for dementia. The READ-OUT Observational
Study investigates blood tests in people seen in memory clinics across the United Kingdom,for a wide
variety of dementias and other memory problems. It will focus a lot of its recruitment from people from
backgrounds that are not often involved in research: very elderly,ethnic minorities,those in deprived
areas or with multiple illnesses,etc. We will also assess whether these tests are good value for money for
the NHS. The project will show if blood biomarkers are useful for people attending NHS memory clinics.
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:
The participant may not enter the study if ANY of the following apply: Lack of venous access Unwilling to consent to NHS data linkage
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Dr
Vanessa
Raymont
vanessa.raymont@psych.ox.ac.uk
Hannah
Rome-Hall
hannah.rome-hall@psych.ox.ac.uk
Hannah
Rome-Hall
hannah.rome-hall@psych.ox.ac.uk
Brandy
Coote
brandycooteconsulting@outlook.com
Brandy
Coote
brandycooteconsulting@outlook.com
The study is sponsored by University of Oxford and funded by ALZHEIMER'S RESEARCH UK .
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 65014
You can print or share the study information with your GP/healthcare provider or contact the research team directly.