Skip to content

SARS-CoV-2 (COVID-19) Longitudinal Study: Understanding Susceptibility, Transmission and Disease Severity (Legacy Study)

SARS-CoV-2 Longitudinal Study: Understanding Susceptibility, Transmission and Disease Severity

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04750356
Enrollment
6000
Registered
2021-02-11
Start date
2021-01-27
Completion date
2024-12-31
Last updated
2022-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

SARS-CoV Infection

Brief summary

The study aims to investigate SARS-CoV-2 susceptibility, transmission and disease severity in healthcare workers and patients. Residual specimens from an existing collection of samples in viral inactivating buffer and derivatives and serum from the Crick COVID-19 Consortium Testing centre (Cohort A1) and additional biological material collected prospectively (Cohorts A2 and B) will be used for research into SARS-CoV-2 transmission, evolution and immune control. This testing centre is a partnership between UCLH and The Francis Crick Institute to provide COVID 19 RT PCR testing for healthcare workers (HCWs) and patients in London Hospitals and care homes. A third group (Cohort C) of the study will allow for collaborative work with other REC approved research studies that have used the Crick COVID-19 Consortium Testing centre and will involve the use of study samples already collected from each study to be analysed under the SARS-CoV-2 Longitudinal Study end points

Interventions

None listed

Sponsors

Francis Crick Institute
CollaboratorOTHER
University College, London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Individuals who have previously provided nasal throat swab samples for SARS-CoV-2 testing at the Crick COVID 19 Consortium Testing centre. * ≥18 years of age * To enrol in the SARS-CoV-2 positive cohort of the study, the participant should have a positive RT qPCR result * Employees based at the participating sites including who had their serology and/or swab tested (for recruitment to Cohort B) * Participants enrolled in other studies who had their samples processed by using the Crick COVID 19 Consortium Testing centre (for recruitment to Cohort C). * Written informed consent (except Cohort A1)

Design outcomes

Primary

MeasureTime frameDescription
SARS-CoV-2 susceptibility in healthcare workers and patients24 monthsTo investigate SARS-CoV-2 susceptibility by examining the number of positive SARS-CoV-2 result per participant
SARS-CoV-2 transmission in healthcare workers and patients24 monthsTo investigate SARS-CoV-2 transmission by analysis of samples sequencing data from each study centre and across study centres
SARS-CoV-2 severity in healthcare workers and patients24 monthsTo investigate SARS-CoV-2 severity by review of symptom severity

Countries

United Kingdom

Contacts

Primary ContactCharles Swanton
crick-legacy@crick.ac.uk020 3796 0000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026