Assessment of Incidence of SARS-CoV-2 Infection and COVID-19 in Brazil (AVISA)

NCT04355338 — Completed, 3520 participants, Butantan Institute

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Assessment of Incidence of SARS-CoV-2 Infection and COVID-19 in Brazil

RegistryNCT04355338, acronym AVISA
StatusCompleted
Study typeObservational
Enrollment3520 (Actual)
SponsorButantan Institute (Other gov)
ConditionsCOVID-19
Datesstart 2020-10-25, primary completion 2021-10-30, completion 2024-10-30, first posted 2020-04-21, last updated 2025-02-06
Locations11 sites in Brazil

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-Summary

This is an observational study, meaning that no interventions is tested, to determine incidence of SARS-CoV-2 infection and COVID-19 in different clinical sites in Brazil in several age groups. The study aims to assess baseline number of infected participants and perform a follow-up along two years to determine the new cases occurring among participants during the period. All participants will collect blood samples to get more details on the immune response.

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+Detailed description

This is an observational longitudinal study to assess incidence of SARS-CoV-2 infection in Brazil. The study sample is stratified in nine age groups according decades of life, equally distributed in both sexes, with an expected incidence of 10%, at least, during the study period of 24 months. For the first age groups, (0-9, 10-19 and 20-29 years), sample was calculated with the minimum expected incidence of COVID-19 among infected, regardless severity, is 10%. For the latest age groups (30-39, 40-49, 50-59, 60-69, 70-79 and 80+), the sample was calculated with the expected minimum incidence of hospitalization due to COVID-19 according to estimates per age group reported by Verity R et al. https://doi.org/10.1016/S1473-3099(20)30243-7 After the consent procedure, all participants will have a short interview, a IgG/IgM SARS-CoV-2 rapid test and a blood withdrawal to obtain serum for neutralizing antibodies. These procedures will be repeated every four weeks until the end of the study. Individuals with symptoms compatible will be followed-up to confirm COVID-19 diagnosis as well as to assess severity, need for hospitalization and assisted ventilation, sequels, and eventual reinfection. Levels of neutralizing antibodies and other immune markers will be prospectively assessed in all infected participants, either asymptomatic and symptomatic.

+Arms and interventions

ArmTypeInterventionsDescription
0-9 yearsParticipants aging 0-9 years
10-19 yearsParticipants aging 10-19 years
20-29 yearsParticipants aging 20-29 years
30-39 yearsParticipants aging 30-39 years
40-49 yearsParticipants aging 40-49 years
50-59 yearsParticipants aging 50-59 years
60-69 yearsParticipants aging 60-69 years
70-79 tearsParticipants aging 70-79 years
80+ yearsParticipants aging 80 years or more

+Outcome measures

Primary outcomes

  • Incidence of SARS-CoV-2 infection [24 months]: Number of cases with serological/virological diagnosis for SARS-Co-2 infection
  • Incidence of COVID-19 [24 months]: Number of cases of symptomatic SARS-CoV-2 infection

Secondary outcomes

  • Incidence of hospitalization due to COVID-19 [24 years]: Number of cases of hospitalization due to symptomatic SARS-Co-2 infection
  • Level of neutralizing antibodies [24 months]: Level of neutralizing antibodies in participants with SARS-Co-2 infection
  • Previous SARS-CoV-2 infection [6 months]: Positive serology for SARS-Co-2 infection at baseline

Other outcomes

  • Incidence of SARS-CoV-2 reinfection [24 months]: Number of a new SARS-CoV-2 infection in an individual with a proven previous infection
  • Incidence of COVID-19 cases requiring mechanical ventilation [24 months]: Number of COVID-19 cases requiring mechanical ventilation
  • Incidence of deaths due to COVID-19 [24 months]: Number of deaths due to COVID-19
  • Incidence of sequels after COVID-19 [24 months]: Number and description of sequels attributed to COVID-19

+Eligibility

Sex: All, accepts healthy volunteers

Inclusion Criteria:

* Any sex or age
* Providing informed consent
* Agreement with all study visits, procedure and contacts

Exclusion Criteria:

* Previous suspected or confirmed COVID-19
* Febrile illness in the latest 72 hours
* Olfactory or gustatory dysfunction in the last three months
* Healthcare worker in a service with routine attention to COVID-19 patients
* Any conditions that can might hurdle participant's compliance to the study in tha opinion of the study team

+Locations (11)

FacilityCityCountryStatus
Universidade Federal do CearáFortaleza, CearáBrazil
Universidade de BrasíliaBrasília, Federal DistrictBrazil
Universidade Federal de Minas GeraisBelo Horizonte, Minas GeraisBrazil
Hospital Universitário Júlio Müller da Universidade Federal de Mato GrossoCuiabá, MountBrazil
Centro de Pesquisas em Medicina Tropical de Rondônia (CEPEM)Porto Velho, RondôniaBrazil
Universidade Federal de Roraima - UFRRBoa Vista, RoraimaBrazil
Universidade Federal de SergipeLaranjeiras, SergipeBrazil
Faculdade de Medicina de São José do Rio Preto - FAMERPSão José do Rio Preto, São PauloBrazil
Faculdade Santa MarcelinaSão Paulo, São PauloBrazil
Hospital Estadual de SerranaSerrana, São PauloBrazil
Instituto de Infectologia Evandro Chagas - FiocruzRio de JaneiroBrazil

+Investigators