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Effectiveness and Adherence to Closed Face Shields to Prevent COVID-19 Transmission (COVPROSHIELD)

26 de abril de 2021 actualizado por: Andrea Ramirez Varela, University of Los Andes, Columbia

Effectiveness and Adherence to Closed Face Shields to Prevent COVID-19 Transmission: A Randomized Controlled Trial

A non-inferiority randomized controlled trial that aims to determine the effectiveness and adherence of the use of closed-face shields and surgical face masks in comparison with the use of surgical face masks for the prevention of SARS-CoV-2 infection in working adults in the city of Bogota, Colombia.

Descripción general del estudio

Descripción detallada

Introduction

According to the Johns Hopkins University coronavirus resource center, COVID-19 has caused more than 1,399,373 deaths globally (as of November 24, 2020), and more than 59 million cases have been reported worldwide. Governments have been forced to establish various preventive measures to control transmission in the communities. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is transmitted among close contacts mainly via respiratory droplets generated when an infected person coughs or sneezes. Likewise, airborne transmission through fomites/aerosols have been described due to the persistence of SARS-CoV-2 on different surfaces and the environment. SARS-CoV-2 causes the coronavirus disease 2019 (COVID-19), the respiratory illness responsible for the ongoing COVID-19 pandemic.

Physical distancing, face mask use, and eye protection had affected stopping SARS-CoV-2 transmission. While there is evidence of the use of face masks as a strategy to control respiratory infections and prevent the inhalation of large droplets and sprays, there is a need to determine the effectiveness of closed-face shields to prevent transmission in community settings. Despite the available reports, none of the randomized clinical trials have been conducted in the community setting. Although scarce, there is promising evidence showing that using face shields may bring an extra benefit in protecting airborne diseases, like COVID-19. Face shields have the benefits of preventing constant contact between face and hands, preventing airflow with possible infected particles from reaching the face, and protecting the eyes.

As of November 24, 2020, more than 1,254,979 cases have been reported in Colombia, and more than 35,479 deaths have occurred (a fatality rate of 2.83%). So far, no massive seroprevalence studies have been carried out in Colombia, that would determine the presence of Immunoglobulin G (IgG) and Immunoglobulin M (IgM) anti-SARS-CoV-2 antibodies, therefore, the level of immunity of the population and the likelihood of further waves of the disease. The first study to determine seroprevalence in Colombia found that, in a sample of 1368 people on the Caribbean coast of Colombia, 55.3% of the participants had anti-SARS-CoV-2 antibodies. The study of seroprevalence that is currently implemented by the Colombian National Institute of Health has not yet yielded results. Bogota, the country's capital district, has the highest number of confirmed cases compared to other departments and cities, but no studies have been conducted to determine what is level of immunity in the city´s population.

Therefore, epidemiological surveillance strategies are carried out to identify asymptomatic and symptomatic patients, trace contacts, and isolate cases to break transmission chains. As a result, an initiative called the CoVIDA project, which enrolls several institutions from academia to hospitals and the health authorities has emerged to support the epidemiological surveillance system of the city. This strategy is based on reverse transcription polymerase chain reaction (RT-PCR) testing for SARS-Cov-2 detection in populations that, because of their work and high mobility in public places, are at high risk of infection and spread of the virus and has contributed to inform the health authorities and help them in the effective decision-making for public policy management.

The CoVIDA project is a study that follows up participants for 21 days and has enrolled more than 33,667 participants since April 2020. The study has included participants whose occupations have high mobility in the community, such as police, military, firefighters, private and public service drivers, shopkeepers, domiciliary, and private security guards, among others. Participants are mostly between 30 and 39 years old, followed by 20 to 29 years old, and there is a lower proportion of the elder population. As of November 24, 2020, from the total of 33,667 participants included in this epidemiological surveillance, 4.35% presented a positive result for the SARS -CoV-2 RT-PCR test.

The present non-inferiority randomized controlled trial aims to determine the effectiveness and adherence of closed face shields plus face mask use compared to face mask use only to prevent SARS -CoV-2 transmission in working adults of Bogota, Colombia.

Methods

Non-inferiority randomized controlled trial nested within a cohort, with a parallel design of 1:1 allocation ratio. Study participants will be recruited through the CoVIDA project that enrolls working adults in Bogota as part of the COVID-19 epidemiologic surveillance. Those who consent to participate in the trial will be randomized for a group wearing closed face shield plus face masks or a group wearing face masks only. Participants will also receive an educational intervention about COVID-19 prevention and the proper use of face shields and face masks. The intervention will last 21 days and includes a COVID-19 symptoms report and verification of protective elements use (adherence). The RT-PCR test and antibody test will be repeated on day 21. A total sample size of 194 participants, 97 per arm, is required to be 80% sure that the upper limit of a one-sided 95% confidence interval (or equivalently a 90% two-sided confidence interval) will exclude a difference in favor of the standard group of more than 5%. If 20% of rejects or losses to follow-up are considered, 233 will be recruited.

Tipo de estudio

Intervencionista

Inscripción (Actual)

233

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Bogotá, Colombia
        • Universidad De Los Andes

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Age 18 years or older
  • Negative RT-PCR test at the beginning of the study.
  • Negative SARS-CoV-2 serological Elecsys Anti-Sars-CoV-2 test at the beginning of the study.
  • Living in a geographic area with active COVID-19 transmission (number of
  • cases reported locally).
  • Living in a geographic area that has been determined by the Colombian National Statistics Department (DANE) to have a medium, medium-high, and high vulnerability index (higher prevalence of comorbidities and social and economic vulnerabilities.
  • Working outside the home for at least two days a week, during the last week.
  • Acceptance to participate in the study regardless of the trial arm assignment through verbal informed consent.

Exclusion Criteria:

  • Retired adults or unemployed
  • Adults referring previous diagnosis of COVID-19 confirmed by RT-PCR tests or serological antibody tests.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Closed face shield + Surgical face mask
Each participant will wear 21 surgical face masks corresponding to the follow-up days in the randomized clinical trial, as well as one closed face shield. Additionally, each participant will receive an educational intervention (video).
Use of a closed face shield with a surgical face mask during daily activities. The educational intervention will provide recommendations on COVID-19 prevention and proper use of the closed face shield and the surgical face masks.
Comparador activo: Surgical face mask
Each participant will wear 21 surgical face masks corresponding to the follow-up days in the randomized clinical trial. Additionally, each participant will receive an educational intervention (video).
Use of a surgical face mask during daily activities. The educational intervention will provide recommendations on COVID-19 prevention and the proper use of surgical face masks.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
COVID-19 incidence
Periodo de tiempo: 21 days of follow-up, RT-PCR test at day 21
The numerator will be the number of cases or the number of persons with laboratory evidence of present infection. In this case, a person with a positive result of a RT-PCR test for SARS-CoV-2 detection. The denominator will be the number of persons allocated in the determined group. Incidence of SARS-CoV-2 infection has been used as a risk measure in several studies, in which comparison groups are made. This risk measure will also allow the calculation of association measures such as RR (relative risk) in both intervention groups.
21 days of follow-up, RT-PCR test at day 21

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Adherence to closed face shields use
Periodo de tiempo: 21 days of follow-up
Adherence to closed face shields is defined as proper daily use of this protective element, which must be worn daily outside the home, and never touch the facial area of the protector. Face shields must be washed daily. Additionally, adherence to face masks is defined as a proper daily use which consists of wearing it covering the nose and mouth, as well as throwing it away daily. A questionnaire intended to evaluate the frequency of use and perception about the advantages of closed face shields and face mask use, as well as the barriers of their use, will be implemented in the participants at the end of the follow-up period.
21 days of follow-up
Percentage of participants with a positive serological test at baseline
Periodo de tiempo: Serological test at day 1
It will be calculated as the number of participants with a positive serological test over the total of people eligible for the clinical trial at baseline.
Serological test at day 1
Percentage of seroconversion in the experimental group and active control group
Periodo de tiempo: Serological test at day 21.
The numerator will be the number of individuals in each group with a positive serological test at end of the study, and the denominator will be the total number of participants assigned to each group.
Serological test at day 21.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Colaboradores

Investigadores

  • Investigador principal: Alejandro Pacheco Gurruchaga, MSc, United Nations
  • Investigador principal: Juan D. Martin, MSc, United Nations
  • Silla de estudio: Luis J. Hernandez Florez, PhD, University of Los Andes, School of Medicine
  • Silla de estudio: Juan J. Yepes Nuñez, PhD, University of Los Andes, School of Medicine
  • Investigador principal: Giancarlo Buitrago Gutierrez, PhD, University of Los Andes
  • Investigador principal: Rachid Laajaj, PhD, University of Los Andes
  • Director de estudio: Eduardo Behrentz, PhD, University of Los Andes
  • Investigador principal: José D. Pinzón, MSc, Pontificia Universidad Javeriana
  • Investigador principal: Jhon M. Gonzalez, PhD, University of Los Andes, School of Medicine
  • Investigador principal: Silvia Restrepo Restrepo, PhD, University of Los Andes

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

16 de enero de 2021

Finalización primaria (Actual)

4 de marzo de 2021

Finalización del estudio (Actual)

4 de marzo de 2021

Fechas de registro del estudio

Enviado por primera vez

24 de noviembre de 2020

Primero enviado que cumplió con los criterios de control de calidad

25 de noviembre de 2020

Publicado por primera vez (Actual)

30 de noviembre de 2020

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

27 de abril de 2021

Última actualización enviada que cumplió con los criterios de control de calidad

26 de abril de 2021

Última verificación

1 de abril de 2021

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

Sí

Descripción del plan IPD

After publication of main results, data will be available for other researchers such as: Study Protocol, Statistical Analysis Plan, Informed Consent Form, Clinical Study Report and Analytic Code.

Marco de tiempo para compartir IPD

6 months after publication

Criterios de acceso compartido de IPD

A formal request sent to the principal investigator.

Tipo de información de apoyo para compartir IPD

  • Protocolo de estudio
  • Plan de Análisis Estadístico (SAP)
  • Formulario de consentimiento informado (ICF)
  • Informe de estudio clínico (CSR)
  • Código analítico

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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