Within Household Transmission of COVID-19 Infections

NCT05430516 | Completed

• 1 other identifier: NL73581.041.20
• Study Type: observational
• Target: 450
• Locations: 1 country
• Sites: 1

Brief Summary

In the absence of a vaccine, the spread of SARS-CoV-2 can only be mitigated via non-pharmaceutical interventions that reduce the risks of forward transmission. Currently, European policymakers are implementing combinations of fierce pandemic control measures. However, there is substantial uncertainty on the transmission dynamics of SARS-CoV-2 and, consequently, the effect of each specific mitigation intervention as well as their joint impact on the pandemic evolution. Moreover, it is uncertain how and when the Public Health response should be modified once the pandemic starts to slow. There is an urgent need for data that can help to further unravel the key transmission characteristics of SARS-CoV-2 in the population. Household studies are, therefore, a useful approach to obtain insight into the main determinants of transmission and to derive estimates of transmission parameters. By fully characterizing the critical process of SARS-CoV-2 household transmission and how they vary by patient and household characteristics, infection dynamics in the population can be further elucidated. Responding to SARS-CoV-2 effectively from a community care perspective will also require understanding the perceptions, beliefs, and actions taken by patients and the public. A 'bottom-up' understating of such issues is critical to understand how best to design effective community strategies. Rapid European COVID-19 Emergency Research response (RECOVER) is a project involving ten international partners that have been selected for funding by the European Union under the Horizon 2020 research framework. RECOVER responds to call topic SC1-PHE-CORONAVIRUS-2020: Advancing knowledge for the clinical and public health response to the SARS-CoV-2 epidemic and builds on many years of investment by the European Commission in clinical research preparedness for epidemic response. RECOVER will therefore provide a range of data and analytical results to guide the Public Health response, including the here described household transmission study. Objective: Estimate key transmission parameters of SARS-CoV-2 in Europe from observing within household virus spread and seroconversion of household members and characterize the views and experiences of households regarding perceptions, practices regarding infection control, and impacts of imposed isolation measures.

Conditions

SARS-CoV-2

Keywords

SARS-CoV-2; Omicron; Children; Household study; Tranmission

Outcome Measures

Primary Outcomes (1)

• Estimate key transmission parameters of SARS-CoV-2 in Europe from observing within household virus spread and seroconversion of household members through study completion, an average of 4 weeks.

  Estimate key transmission parameters of SARS-CoV-2 in Europe from observing within household virus spread and seroconversion of household members. Including secondary attack rates and Transmission rate.

  Samples and data collected through study completion, an average of 4 weeks.

Secondary Outcomes (6)

• Estimate the incubation period through study completion, an average of 4 weeks.

  Samples and data collected through study completion, an average of 4 weeks.

• Estimate the generation time through study completion, an average of 4 weeks.

  Samples and data collected through study completion, an average of 4 weeks.

• Estimate the susceptibility through study completion, an average of 4 weeks.

  Samples and data collected through study completion, an average of 4 weeks.

• Estimate the infectiousness through study completion, an average of 4 weeks.

  Samples and data collected through study completion, an average of 4 weeks.

• Estimate the transmission through study completion, an average of 4 weeks.

  Samples and data collected through study completion, an average of 4 weeks.

Study Arms (1)

Families

Patients with confirmed SARS-Cov-2 infection and their household members of all ages can be enrolled in the study, if at least one household member is a child age under 18.

Other: No intervention

Interventions

No intervention OTHER

No intervention

Families

Eligibility Criteria

• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Communty within the region of Utrecht

You may qualify if:

• All members of the household or their legal guardians consent to participation
• All members of the household are willing to complete diaries and questionnaires for the duration of follow-up

You may not qualify if:

• Patients or household members who are unable to consent, or do not wish to provide informed consent.
• Children, pregnant women and patients lacking capacity will be included. Those lacking capacity to consent for themselves will be identified and consent will be sought from an appropriate consulted.
• Households who do not have daily access to a smartphone or tablet with internet connection, will be excluded, as follow-up of households requires the use of an interactive diary App.

Sponsors & Collaborators

• UMC Utrecht: lead

Study Sites (1)

UMC Utrecht

Utrecht, 3584CX, Netherlands

Location

Study Officials

• Patricia Bruijning, MD PhD

  UMC Utrecht

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: March 17, 2022
• First Posted: June 24, 2022
• Study Start: January 15, 2022
• Primary Completion: May 1, 2022
• Study Completion: May 1, 2022
• Last Updated: June 24, 2022

Record last verified: 2022-06

Locations

NL (1)