Ask to take part

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.

Contact Information:

Prof Patrick T. Kennedy
+44 (0)207 882 6187
p.kennedy@qmul.ac.uk


Study Location:

Skip to Main Content

Keep up to date

Sign up for news and information about taking part and shaping research.

English | Cymraeg
Be Part of Research - Trial Details - Coronavirus (COVID-19) antibody response in healthcare staff: What proportion of healthcare staff have COVID-19 antibodies? How long do the antibodies last? Do the antibodies protect against recurring infection?

Coronavirus (COVID-19) antibody response in healthcare staff: What proportion of healthcare staff have COVID-19 antibodies? How long do the antibodies last? Do the antibodies protect against recurring infection?

Not Recruiting

Open to: All Genders

Age: Adult

Medical Conditions

COVID-19 (SARS-CoV-2 infection) antibody response in healthcare workers


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.


COVID-19 is a condition caused by the coronavirus (called SARS-CoV-2) that was first identified in late 2019. This virus can infect the respiratory (breathing) system. Some people do not have symptoms but can carry the virus and pass it on to others. People who have developed the condition may develop a fever and/or a continuous cough among other symptoms. This can develop into pneumonia. Pneumonia is a chest infection where the small air pockets of the lungs, called alveoli, fill with liquid and make it more difficult to breathe.

In 2020, the virus has spread to many countries around the world and neither a vaccine against the virus or specific treatment for COVID-19 has yet been developed. As of March 2020, it is advised that people minimize travel and social contact, and regularly wash their hands to reduce the spread of the virus.

Groups who are at a higher risk from infection with the virus, and therefore of developing COVID-19, include people aged over 70 years, people who have long-term health conditions (such as asthma or diabetes), people who have a weakened immune system and people who are pregnant. People in these groups, and people who might come into contact with them, can reduce this risk by following the up-to-date advice to reduce the spread of the virus.

Antibodies detected by blood tests indicate that a person has been exposed to SARS-CoV-2 and developed antibodies as part of an immune response to the virus. Antibody tests are important to confirm prior infection, including in individuals with few or no symptoms. There are several different classes (or types) of antibody which may develop in response to any infection. These include immunoglobulin G (known as IgG) and immunoglobulin M (known as IgM).

This study will measure antibodies to COVID-19 in up to 2000 healthcare workers at Barts Health NHS Trust. The percentage of healthcare workers who have been exposed to the SARS-CoV-2 virus and who have developed antibodies will be reported. A proportion of the study participants will be called back for study visits at 3 months and at 6 months after enrolment. The aim of the follow-up visits is to measure how long the antibodies last, and also to determine if having antibodies to COVID-19 protects against getting COVID-19 disease a second time.

In the study, the COVID-19 antibodies will be measured using the Panbio™ COVID-19 IgG/IgM Rapid Test. The Panbio™ COVID-19 IgG/IgM Rapid Test is a test that uses a small drop of blood to detect IgG and IgM antibodies to SARS-CoV-2. Different types of human fluid samples including blood taken from a vein (venous whole blood), blood from a fingerstick (capillary whole blood) and serum or plasma (which are fluids prepared in a lab by processing whole blood samples) can be used on the Panbio™ COVID-19 IgG/IgM Rapid Test The test is interpreted 10-20 minutes after sample application. The result is qualitative, meaning it shows that the antibodies are, or are not, present, rather than giving a value or number to measure the antibodies. In the study, a positive test result will be confirmed by laboratory testing of the same blood sample using the Abbott Architect or Roche Elecsys SARS-CoV-2 antibody tests.

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:

02 Jun 2020 21 Aug 2020

Publications

2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33987193/ 3-month follow-up results (added 28/01/2022)

During the initial study visit and follow-up visits, the study participants will be asked for a brief medical history, focussed on COVID-19 risk factors, past COVID-19 symptoms and COVID-19 testing. One tube of venous blood will be taken from each participant at each visit. Study participants are also asked to notify the study team of any potential COVID-19 symptoms that occur between visits by sending a message to a secure email address.


Healthcare workers at Barts Health NHS Trust can participate in the study. This includes frontline staff such as doctors and nurses as well as administrative staff and other non-clinical staff.

You can take part if:



You may not be able to take part if:


1. Previously participated in this study on a previous occasion2. Unable or unwilling to provide informed consent3. Is a vulnerable person as deemed unfit for the study by the Principal Investigator4. Current symptoms of COVID-19 or has had COVID-19 symptoms within the last 14 days


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Barts Health NHS Trust
    Whitechapel Rd London E1 1BB
    London
    E1 1BB

The study participants will receive their COVID-19 antibody result. It is possible that the collection of blood could cause discomfort. However, as this is a routine medical procedure and the samples will be obtained by trained medical personnel, the discomfort is likely to be minimized. COVID-19 transmission is a risk to the participants. However, convalescent patients are not expected to be transmitting the virus. Symptomatic participants, or participants with COVID-19 symptoms during the last 14 days are excluded from the study. All operations will be conducted under strict social distancing to minimize the risk of transmission.

Prof Patrick T. Kennedy
+44 (0)207 882 6187
p.kennedy@qmul.ac.uk



The study is sponsored by Abbott (Germany) and funded by Abbott Rapid Diagnostics Jena GmbH.




We'd like your feedback

Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.


Is this study information helpful?

What will you do next?

Read full details for Trial ID: ISRCTN15634328

Or CPMS 46155

Last updated 28 January 2022

This page is to help you find out about a research study and if you may be able to take part

You can print or share the study information with your GP/healthcare provider or contact the research team directly.