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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.
Kate
Cowen
kate.cowen@durham.ac.uk
Kathleen
Vancleef
kathleen.vancleef@durham.ac.uk
John
Mulcahy
john.mulcahy@nhs.net
Cerebrovascular diseases
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.
There is a high prevalence of stroke survivors with visual perception difficulties which is often un-diagnosed. Clinicians working in stroke settings have indicated that a screening tool,ideally taking 15-minute to administer would improve diagnosis. Therefore,a screening tool,the Oxford Visual Perception Screening (OxVPS) has been created to assess for visual perception problems following stroke. This screening tool now needs to be tested.
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: Cross-sectional;
You can take part if:
You may not be able to take part if:
Insufficient understanding of English Clinical concerns that patient is unable follow simple instructions. Clinical concerns that patient is unable to concentrate for 15 minutes. No capacity to provide informed consent.
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
John
Mulcahy
john.mulcahy@nhs.net
Kathleen
Vancleef
kathleen.vancleef@durham.ac.uk
Kate
Cowen
kate.cowen@durham.ac.uk
The study is sponsored by COUNTY DURHAM AND DARLINGTON NHS FOUNDATION TRUST and funded by NIHR Academy .
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 56457
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
