COVID-19 (SARS-CoV-2 infection) Infections and Infestations
Conditions
Interventions
All participants will receive the three-time intervention after they have given their consent/assent. The researchers will take a medical history from participants/parents/carer and physically examine
Sponsors
Diponegoro University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Children aged under 18
Exclusion criteria
Exclusion criteria: Children without parent/legal guardian permission
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mucosal immunity of SARS-COV-2 measured using fluorescent-bead-based multiplex immunoassay at baseline, 14 and 28 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Disease symptoms measured using physical examination and anamnesis (COVID-19-related symptoms 14 days before sample collection, contact history, and comorbidities), recorded at baseline, 14, and 28 days. | — |
Countries
Indonesia
Outcome results
None listed