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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.
COVID-19 Post-Acute COVID-19 Syndrome Lung Diseases Lung Diseases, Interstitial
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.
Prospective observational study of hospitalised and non-hospitalised patients post- infection with SARS-CoV-2. The study aims to recruit 2000 individuals, with proven COVID-19, who were not hospitalised but presented to Long-COVID clinics with persistent respiratory symptoms such as breathlessness or cough and are referred for cross-sectional imaging (computer tomography, CT) at baseline (3 months weeks after their first COVID-19 symptoms). The study will run for 18 months.
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:
You can take part if:
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
mark weeks, Dr
+44 (0)20 7594 7972
m.weeks@imperial.ac.uk
The study is sponsored by Imperial College London and is in collaboration with Medical Research Council; University of Nottingham; University of Southampton; University of Leicester; University of Manchester; University of Liverpool; University of Sheffield; University of Oxford; University College, London; University of Newcastle Upon-Tyne; University of Edinburgh.
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
