COVID-19 (SARS-CoV-2 infection) Infections and Infestations
Conditions
Interventions
1. Online consent, baseline data collection
2. Online daily symptom diary - for 3 months
3. Self-sampling upper respiratory tract (nose, throat & saliva) - twice weekly for 3 months
4. Blood sampling
Sponsors
University of Bristol
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Any patient-facing clinical staff member working regularly in the Children’s Emergency Department (CED) of Bristol Royal Hospital for Children, including doctors, nurses and healthcare assistants
Exclusion criteria
Exclusion criteria: 1. Staff who, on average, work less than two shifts per week 2. Staff who anticipate that they will not able to complete at least 6 weeks of the study, excluding annual leave e.g. about to go on maternity leave
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| COVID-19 symptoms measured using online daily symptom diary every day for 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. COVID-19 infection measured using self-sampling of upper respiratory tract (nose, throat & saliva) - twice weekly for 3 months 2. Serum antibody levels and peripheral antigen-specific memory T cells measured using blood sampling at weeks 0, 6, 12, 18, and 52 | — |
Countries
England, United Kingdom
Outcome results
None listed