COvid-19 National Survey for Assessing VIral Spread by Nonaffected CarriErs (CON-VINCE)
- Conditions
- COVID19
- Registration Number
- NCT04379297
- Lead Sponsor
- Luxembourg Institute of Health
- Brief Summary
CON-VINCE (COvid-19 National survey for assessing VIral spread by Non-affected CarriErs) is a national, monocentric, and longitudinal study aiming to evaluate the spread dynamics of the COVID-19 disease within the Luxembourgish population. Participants who are clinically asymptomatic or present with only mild symptoms will be followed up longitudinally, regularly tested for SARS-CoV-2 by RT-PCR, antibody status, and subjected to an epidemiological, clinical and biological phenotyping to better understand the nature, dynamics of infectivity and spread of the virus in the population. CON-VINCE will also track the psychological and socio-economic impact of long-term containment measures on the general population.
- Detailed Description
To capture the dynamics and impact of the virus spread in the Luxembourgish population, data and sample collection is done every two weeks for two months (4 times in total) with a final follow-up one year after the participant's inclusion in the study. Participants complete questionnaires before each sample collection. The baseline questionnaire captures demographic data, medical history, behavioral and psychological data, and socio-economic status. Participants provided information on medical history, history of allergies, smoking, and chronic medication taken regularly. COVID-19-related data and environmental conditions of the household were obtained.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1870
- Subjects aged 18 and older of both genders, with a full capacity of consent.
- SARS-CoV-2-positive individuals with an asymptomatic or oligosymptomatic infection (mild or oligosymptomatic disease course is defined as absence of fever and respiratory distress or cough not attributable to other known chronic disease).
- OR SARS-CoV-2-negative individuals at the time of inclusion.
- OR post-infectious SARS-CoV-2-negative individuals with acquired immunity to SARS-CoV-2 and a mild disease course.
- Evolution of the COVID-19 disease requiring a hospital admission before inclusion in the study
- Presence of fever and respiratory distress/cough at the time of inclusion not attributable to other known chronic disease
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Prevalence and dynamics of the SARS-COV 2 infection in Luxemburg 04.2020-05.2021 Evaluation of the prevalence by RT-PCR and serology testing
Collection of samples for research 04.2020-05.2021 Samples will be analysed and stored for future research
- Secondary Outcome Measures
Name Time Method Psycho-social evaluation 04.2020-05.2021 Psychological and socio- economic impact of long-term containment measures on the general population
Trial Locations
- Locations (1)
Luxembourg Institute of Health
🇱🇺Strassen, Luxembourg