Severe Acute Respiratory Syndrome Coronavirus 2 InfectionNCT05458557
Antigen Rapid Diagnostic Tests for Community Identification of Severe Acute Respiratory Syndrome Coronavirus 2
An observational study of Severe Acute Respiratory Syndrome Coronavirus 2 Infection, run by Elizabeth Glaser Pediatric AIDS Foundation at 1 site in Kenya.
Trial summary
Background: Background: Testing with antigen-detecting rapid diagnostic tests (Ag-RDTs), including in asymptomatic individuals, has the potential to promptly identify more Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infections and consequently decrease spread of coronavirus-19 disease at the community… Read more about this study
- Who is it for?
- Ages 2 years and olderHealthy volunteers can take part
- Conditions the study is for
- Severe Acute Respiratory Syndrome Coronavirus 2 Infection
- What is being tested?
- Rapid Antigen Testing
- How many people
- 5,000 participants
- Where
- 1 siteKenya
- Study dates
- 20 Jun 2022to 16 Dec 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 2 years and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: The study population will be composed of all persons attending the selected venue where testing is offered on the day of the testing campaign, including all ages > 2 years regardless of presence of coronavirus-19 symptoms. This population will include people from different economic and social backgrounds.
Who may be able to join
- Age > 2 years
- Agrees to Undergo testing with SARS-CoV-2-Ag RDT on the day of testing campaign
- Ability and willingness to provide written consent/assent for participation in an interview following the test
Who cannot join
- 1. Positive SARS-CoV-2 test done 1 to 14 days before the current testing campaign
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Evaluation of Antigen Rapid Diagnostic Tests (Ag-RDTs) for Community Identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in Kiambu County, Kenya
Background:
Background: Testing with antigen-detecting rapid diagnostic tests (Ag-RDTs), including in asymptomatic individuals, has the potential to promptly identify more Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infections and consequently decrease spread of coronavirus-19 disease at the community level. In addition, rapid test results are important for immediate clinical management and isolation of patients with SARS-CoV-2 infection, and for contact tracing and quarantining of contacts. Data on SARS-CoV-2 infection rates, the acceptability of Ag-RDT, and the cost of conducting widespread testing in these communities are limited in Africa.
Read more
Study Aim and Objectives: To generate evidence evaluating the use of Ag-RDTs for community identification of SARS-CoV-2 infections within large gathering venues such as work places, schools, places of worship, and markets.
The primary objective is to determine the SARS-CoV-2 case detection rate through a mass testing approach in large gatherings. Secondary objectives include determining the proportion of asymptomatic and symptomatic infections detected, acceptance of mass SARS-CoV-2 Ag-RDT testing, the prevalence of circulating variants, and the cost of implementing this community testing strategy.
Study Design: The investigators propose a serial cross-sectional study design targeting approximately 15,000 persons, who will be offered testing in up to 50 different high attendance venues of Kiambu County that will be identified as possible points of community-based transmission. The study will follow an opt-in consent approach, with those accepting to participate providing additional information to the trained research assistant and/or health worker.
Outcome: Evidence will be generated to provide recommendations to the Kenya Ministry of Health, and more broadly to inform the field on the use of Ag-RDTs for large scale community screening by identifying best practices and stratifying risk areas for community transmission based on rates of infections detected within various settings.
Read the detailed description
Study context
Since 31 March 2020, when the first case was confirmed in the country, a total of 20144 confirmed cases and 877 deaths (case fatality rate of (4.4%) have been line-listed as of 27th February 2022. Kiambu ranks second in cumulative number of confirmed Coronavirus-19 cases. Kiambu county has major gaps in Coronavirus-19 management due to inadequate resources limiting response capacity in detecting, investigating, contact tracing and follow up both in the facilities and within the community. The county has reported spikes in cases of Coronavirus-19 following participation in mass gathering events like in political rallies, markets, churches, burials, etc. The county has several tertiary institutions which have also been identified as high transmission hotspots. Kiambu county implements the Coronavirus-19 guidelines as stipulated in the ministry of health guidelines (hand washing, social distancing, use of masks etc), but non-compliance with Coronavirus-19 protocols has been noted in learning institutions and public places like Bus parks, markets and supermarkets.
The Elizabeth Glaser Pediatric AIDS Foundation (EGPAF) is supporting the Ministry of Health (MOH) in Kenya to accelerate an effective Coronavirus-19 response through novel solutions to increase access to high quality diagnostics and therapeutics through the Unitaid-funded Catalysing Coronavirus-19 Action (CCA) project. As part of this project, EGPAF is supporting decentralizing testing through integration of severe acute respiratory syndrome Coronavirus-2 (SARS-CoV-2) antigen rapid diagnostic test (Ag RDT) into Maternal Newborn Child Health, Tuberculosis and HIV clinics in about 31 facilities of Kiambu county. The project also enhances linkage to care and treatment including new therapeutics through a hub and spoke model. EGPAF works with civil society organizations and other key stakeholders in Kiambu county to increase demand for SARS-CoV-2 testing and care and treatment. This study will build upon the programmatic components of the CCA project to explore the effectiveness of SARS-CoV-2 AgRDT mass testing in high volume community venues to detect SARS-CoV-2 infections. The CCA project has been implemented since October 2021 with testing using Ag-RDT since January 2022 in Kiambu county. It has been observed that a number of clients attending facilities in services where the test is not currently offered are asking for testing, and during community vaccination campaigns, people are asking for the possibility to be tested.
Study Rationale As of 14 March 2022, 28.8% of adults were fully vaccinated in Kenya 4. Until vaccines have widespread availability, testing and isolation are the best methods to control disease spread at the national level. The use of simple, rapid, and affordable Ag-RDT to expand access to SARS-CoV-2 testing is being incorporated in many national Coronavirus-19 responses. Targeting high volume community venues has the potential to screen a lot of people within a limited amount of time and determine areas that are contributing to community transmission. Data on acceptability of mass SARS-CoV-2 Ag-RDT testing in these community settings in Africa are limited.
Most current programs use a screen and test strategy to identify symptomatic infection and those at risk due to exposure because of the limited availability and costs of broader testing. However, this strategy does not identify those with asymptomatic infection who also contribute to the spread of SARS-CoV-2 infection. Data are needed to inform the evolving SARS-CoV-2 testing guidelines and provide MOH with feasible and costed testing models to address their national strategies. This study will generate the evidence needed to determine the SARS-CoV-2 case detection rate and proportion of asymptomatic and symptomatic infections detected in high volume community venues using SARS-CoV-2 Ag-RDTs. Additionally, full genome sequencing of positive cases will be useful to the MoH in determining the circulating genomic strains in Kenya at real time and may contribute to national guidance.
Study Aim:
The aim of this study is to generate evidence evaluating the use of Ag-RDTs for community identification of SARS-CoV-2 infections within large gathering venues, and ultimately to determine if mass testing in such venues is a feasible and useful approach.
Primary Objective:
1.To estimate the SARS-CoV-2 case detection rate (number of SARS-CoV-2 infections detected per 100 individuals tested) in high volume community venues using SARS-CoV-2 Ag-RDT, overall and disaggregated by venue type.
Secondary Objectives:
To determine the number and proportion of venue attendees across the SARS-CoV-2 testing cascade: people offered Ag-RDT, who accept testing, receive test results, test positive, To determine the number and proportion of people who test positive with SARS-CoV2 RDT who are symptomatic, are referred for polymerase chain reaction (PCR) testing and confirmed with PCR, are referred for home-based isolation or care, To identify factors that are associated with SARS-CoV-2 infection, such as age, venue, exposure history and vaccination status.
To describe SARS-CoV-2 variants among SARS-CoV-2 positive attendees To determine costs associated with implementation of SARS-CoV-2 Ag-RDT in community settings.
The investigators hypothesize that with the introduction of SARS-CoV-2 mass testing in high-exposure venues in the community, more individuals will have access to testing services, individuals will accept SARS-CoV-2 Ag RDT, symptomatic and asymptomatic SARS-CoV-2 infections will be diagnosed, and individuals diagnosed with SARS-CoV-2 will be linked to care and treatment services. This will lead to isolation of SARS-CoV-2 infected individuals, quarantining of contacts, and medical treatment for those requiring it.
Study Design This will be a community-based cross-sectional study. The study will be conducted among the population of Kiambu County, central Kenya, attending specific high-volume community venues identified as possible points of community-based transmission.
These high-volume community venues will be:
Venues identified by individuals diagnosed with SARS-CoV-2 infection in a subset of CCA-supported facilities in Kiambu County. As part of the CCA questionnaire, participants will be asked to identify crowded places the participants had been to in the 10 days prior to their positive SARS-CoV-2 test. This will provide an opportunity for the staff to identify market places, places of worship, schools, or other venues where SARS-CoV-2 transmission is likely to occur in the communities. In this study, no testing activities will be conducted in health facilities.
Venues identified in collaboration with the department of public health and the Coronavirus-19 response team in the county that may act as transmission hotspots.
Using both approaches above, the investigators will identify venues in Kiambu county where a large number of people congregate to propose mass testing.
Variant surveillance population Individuals who test positive with SARS-Cov-2 Ag-RDT and those who test negative but with symptoms of Coronavirus-19 will be asked to provide a second sample for confirmatory PCR testing and whole genome sequencing for variant surveillance. The participants will be taken care of as Coronavirus-19 cases as the participant wait for the PCR result. Based on the national guidelines on management of Coronavirus-19 in Kenya, a person who meets the clinical and epidemiological criteria is a suspected case of SARS-CoV-2. The participant will be assessed and based on the severity of their symptoms the participant will either be referred to a treatment centre where symptoms will be managed. If the person has mild symptoms he will be referred for home based care. The study team will transport those who need to be hospitalized to the hospital. Kiambu county currently has 5 treatment centres which also act as isolation centres. While secondary sample collection is part of routine national surveillance, because these results will be used for research purposes, the investigators will only perform this study activity for those who voluntarily agree to this study through administration of a written informed consent. The second sample will be taken at the community venue for those who will have given written consent/assent and transported to the testing laboratory in accordance with the standard operating procedures.
Inclusion criteria for variant surveillance:
Venue attendee with a positive result to SARS-Cov-2 Ag-RDT Venue attendee with a negative Ag-RDT, but with Coronavirus-19 symptoms Provide written informed consent to collect a second sample Community mobilization and recruitment This section describes activities conducted by Kiambu County Coronavirus-19 response team ahead of the start of study activities.
Mobilizing the community to ensure a high response rate is a priority for successful study implementation the Kiambu County Coronavirus-19 response team will be engaged from the initial stages to ensure that the security coordination mechanisms are well informed.
Before the mass testing, meetings will be held with the community leaders to explain the study and have the opportunity to discuss potential problems and concerns, including preventing dissemination of false information. These meetings will be coordinated by the public health department in the county in strong collaboration with the EGPAF team. Depending on the venue, key stakeholders may include social workers, community health volunteers, local community leaders (chiefs, sub chiefs), members of the county and sub- county health management teams, including those from the public health department, county Coronavirus-19 response manager, county education department, school principals, religious leaders, among others. Ongoing dialogue with these stakeholders will be important to maintain community engagement before and during the study implementation.
A few days before the start of testing campaign, community health volunteers will visit the selected high attendance venues and a poster announcing the community testing activity will be distributed for display in the venue prior to the scheduled testing intervention.
Trained community health volunteers and mobilizers will present to the venue on the pre-agreed day(s) to announce the actual testing day and mobilize the community. Available channels like community, Facebook, and other social media will also be used to mobilize the community. Through church leaders and association of pastors, messages about the testing will be posted on church websites where available. Megaphones and caravans may also be used for community mobilization as deemed appropriate.
Data Collection on the day of testing, individuals accessing the venue will be informed of the SARS-CoV-2 testing taking place and asked if the participants are willing to be tested. An anonymous screening log will be completed for all individuals offered testing, which will include age, sex, whether testing was accepted or not, and any reported reasons for choosing not to test. This will allow capture of a brief description of the population at each venue and documentation of the testing refusal rate.
For those who opt in for testing, the MoH staff will provide routine information on the test procedure before performing the test (see section on testing procedure). During the consenting process, information about the study objectives and procedures will be provided and the client will be able to ask questions. Those who agree will then undergo a 2- to 5-minutes interview. The data obtained from the interview will be recorded in the data collection tool and later entered into the study database.
For individuals tested positive and those negative referred for PCR because of Coronavirus-19 symptoms, the investigators will also collect information on their final PCR result, and the result of their sequencing test after obtaining from them a written informed consent.
PCR/whole genome sequencing (WGS) surveillance:
Kenya Medical Research Institute-Wellcome Trust Research Laboratory in Kilifi is currently the laboratory tasked by the Ministry of Health with SARS-CoV-2 genome sequencing in Kenya. The laboratory operates in compliance with Good Clinical Laboratory Practice (GCLP) standards. For this study, the Coronavirus-19 sequencing sample manifest form (QMS-F238- Annex 5) will be completed with all the required information and sent together with the swabs to Kenya Medical Research Institute-Wellcome Trust Research Laboratory. Laboratory staff will communicate results to the study team using the unique identifiers described above; the study team will update the study database.
Costs will be estimated from a health systems perspective using a micro-costing method, combining top-down and bottom-up approaches to obtain resource use and costs per line item. All project costs will be converted to 2022 U.S. dollars (US$) using the prevailing exchange rate and adjusted to inflation using the U.S. consumer price index if needed.
- Being tested
- Rapid Antigen Testing
- Medical subject headings
- COVID-19
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Rapid Antigen TestingDiagnostic test
Community testing for SARS-COV-2 using rapid Antigen test
What is being measured
The primary outcome is the main question the study is designed to answer.
SARS-CoV-2 case detection rate
Will determine the proportion of SARS-CoV-2 infections detected per 100 individuals tested) in high volume community venues using SARS-CoV-2 Ag-RDT, overall and disaggregated by venue type.
Measured: This will be done in a period of 4 months of study enrolment
Secondary outcomes (5)
Proportion testing positive across the cascade
will determine proportion of venue attendees across the SARS-CoV-2 testing cascade
Measured: 4 months
Positive cases by type
Proportion of people who test positive with SARS-CoV2 RDT who are symptomatic, are referred for PCR and confirmed with PCR, are referred for home-based isolation or care,
Measured: 4months
Factors
Factors that are associated with SARS-CoV-2 infection, such as age, venue, exposure history and vaccination status.
Measured: 4 months
SARS-COV-2 variants
SARS-CoV-2 variants among SARS-CoV-2 positive attendees
Measured: 4 months
Costing
Costs associated with implementation of SARS-CoV-2 Ag-RDT in community settings.
Measured: 4months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Jul 2022
- Study start20 Jun 2022
- Primary completion30 Sep 2022
- Study completion16 Dec 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Severe Acute Respiratory Syndrome Coronavirus 2 InfectionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 5,000 participants (actual)
Sponsor and investigators
- Lead sponsor
- Elizabeth Glaser Pediatric AIDS Foundation
- Sponsor type
- University, hospital or other
- Collaborators
- Find, Kiambu County
- Responsible party
- Principal investigator, Rose Otieno Masaba, Elizabeth Glaser Pediatric AIDS Foundation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05458557
- Sponsor's protocol ID
- EG0278
- Status last verified
- Apr 2023
- First submitted
- 7 Jul 2022
- Last updated
- 19 Apr 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Masaba R, Siamba S, Hoffman HJ, Osire E, Kimani N, Kwasa M, Songane M, Denoeud-Ndam L. A Cross-Sectional Study of the Use of Antigen Rapid Diagnostic Tests for Community Identification of SARS-CoV-2 in Kenya. Am J Trop Med Hyg. 2024 Nov 26;112(4_Suppl):17-25. doi: 10.4269/ajtmh.23-0756. Print 2025 Apr 1.
PubMed 39591654
Study at a glance
From the registry record, last updated by the sponsor on 19 Apr 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Antigen Rapid Diagnostic Tests (Ag-RDTs) for Community Identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in Kiambu County, Kenya
- ClinicalTrials.gov ID
- NCT05458557
- Acronym / sponsor ID
- EG0278
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 5,000 participants (actual)
- Lead sponsor
- Elizabeth Glaser Pediatric AIDS FoundationUniversity, hospital or other
- Collaborators
- Find, Kiambu County
- Study start
- 20 Jun 2022 (actual)
- Primary completion
- 30 Sep 2022 (actual)
- Study completion
- 16 Dec 2022 (actual)
- First posted
- 14 Jul 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background:
Background: Testing with antigen-detecting rapid diagnostic tests (Ag-RDTs), including in asymptomatic individuals, has the potential to promptly identify more Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infections and consequently decrease spread of coronavirus-19 disease at the community level. In addition, rapid test results are important for immediate clinical management and isolation of patients with SARS-CoV-2 infection, and for contact tracing and quarantining of contacts. Data on SARS-CoV-2 infection rates, the acceptability of Ag-RDT, and the cost of conducting widespread testing in these communities are limited in Africa.
Study Aim and Objectives: To generate evidence evaluating the use of Ag-RDTs for community identification of SARS-CoV-2 infections within large gathering venues such as work places, schools, places of worship, and markets.
The primary objective is to determine the SARS-CoV-2 case detection rate through a mass testing approach in large gatherings. Secondary objectives include determining the proportion of asymptomatic and symptomatic infections detected, acceptance of mass SARS-CoV-2 Ag-RDT testing, the prevalence of circulating variants, and the cost of implementing this community testing strategy.
Study Design: The investigators propose a serial cross-sectional study design targeting approximately 15,000 persons, who will be offered testing in up to 50 different high attendance venues of Kiambu County that will be identified as possible points of community-based transmission. The study will follow an opt-in consent approach, with those accepting to participate providing additional information to the trained research assistant and/or health worker.
Outcome: Evidence will be generated to provide recommendations to the Kenya Ministry of Health, and more broadly to inform the field on the use of Ag-RDTs for large scale community screening by identifying best practices and stratifying risk areas for community transmission based on rates of infections detected within various settings.
Detailed description
Study context
Since 31 March 2020, when the first case was confirmed in the country, a total of 20144 confirmed cases and 877 deaths (case fatality rate of (4.4%) have been line-listed as of 27th February 2022. Kiambu ranks second in cumulative number of confirmed Coronavirus-19 cases. Kiambu county has major gaps in Coronavirus-19 management due to inadequate resources limiting response capacity in detecting, investigating, contact tracing and follow up both in the facilities and within the community. The county has reported spikes in cases of Coronavirus-19 following participation in mass gathering events like in political rallies, markets, churches, burials, etc. The county has several tertiary institutions which have also been identified as high transmission hotspots. Kiambu county implements the Coronavirus-19 guidelines as stipulated in the ministry of health guidelines (hand washing, social distancing, use of masks etc), but non-compliance with Coronavirus-19 protocols has been noted in learning institutions and public places like Bus parks, markets and supermarkets.
The Elizabeth Glaser Pediatric AIDS Foundation (EGPAF) is supporting the Ministry of Health (MOH) in Kenya to accelerate an effective Coronavirus-19 response through novel solutions to increase access to high quality diagnostics and therapeutics through the Unitaid-funded Catalysing Coronavirus-19 Action (CCA) project. As part of this project, EGPAF is supporting decentralizing testing through integration of severe acute respiratory syndrome Coronavirus-2 (SARS-CoV-2) antigen rapid diagnostic test (Ag RDT) into Maternal Newborn Child Health, Tuberculosis and HIV clinics in about 31 facilities of Kiambu county. The project also enhances linkage to care and treatment including new therapeutics through a hub and spoke model. EGPAF works with civil society organizations and other key stakeholders in Kiambu county to increase demand for SARS-CoV-2 testing and care and treatment. This study will build upon the programmatic components of the CCA project to explore the effectiveness of SARS-CoV-2 AgRDT mass testing in high volume community venues to detect SARS-CoV-2 infections. The CCA project has been implemented since October 2021 with testing using Ag-RDT since January 2022 in Kiambu county. It has been observed that a number of clients attending facilities in services where the test is not currently offered are asking for testing, and during community vaccination campaigns, people are asking for the possibility to be tested.
Study Rationale As of 14 March 2022, 28.8% of adults were fully vaccinated in Kenya 4. Until vaccines have widespread availability, testing and isolation are the best methods to control disease spread at the national level. The use of simple, rapid, and affordable Ag-RDT to expand access to SARS-CoV-2 testing is being incorporated in many national Coronavirus-19 responses. Targeting high volume community venues has the potential to screen a lot of people within a limited amount of time and determine areas that are contributing to community transmission. Data on acceptability of mass SARS-CoV-2 Ag-RDT testing in these community settings in Africa are limited.
Most current programs use a screen and test strategy to identify symptomatic infection and those at risk due to exposure because of the limited availability and costs of broader testing. However, this strategy does not identify those with asymptomatic infection who also contribute to the spread of SARS-CoV-2 infection. Data are needed to inform the evolving SARS-CoV-2 testing guidelines and provide MOH with feasible and costed testing models to address their national strategies. This study will generate the evidence needed to determine the SARS-CoV-2 case detection rate and proportion of asymptomatic and symptomatic infections detected in high volume community venues using SARS-CoV-2 Ag-RDTs. Additionally, full genome sequencing of positive cases will be useful to the MoH in determining the circulating genomic strains in Kenya at real time and may contribute to national guidance.
Study Aim:
The aim of this study is to generate evidence evaluating the use of Ag-RDTs for community identification of SARS-CoV-2 infections within large gathering venues, and ultimately to determine if mass testing in such venues is a feasible and useful approach.
Primary Objective:
1.To estimate the SARS-CoV-2 case detection rate (number of SARS-CoV-2 infections detected per 100 individuals tested) in high volume community venues using SARS-CoV-2 Ag-RDT, overall and disaggregated by venue type.
Secondary Objectives:
To determine the number and proportion of venue attendees across the SARS-CoV-2 testing cascade: people offered Ag-RDT, who accept testing, receive test results, test positive, To determine the number and proportion of people who test positive with SARS-CoV2 RDT who are symptomatic, are referred for polymerase chain reaction (PCR) testing and confirmed with PCR, are referred for home-based isolation or care, To identify factors that are associated with SARS-CoV-2 infection, such as age, venue, exposure history and vaccination status.
To describe SARS-CoV-2 variants among SARS-CoV-2 positive attendees To determine costs associated with implementation of SARS-CoV-2 Ag-RDT in community settings.
The investigators hypothesize that with the introduction of SARS-CoV-2 mass testing in high-exposure venues in the community, more individuals will have access to testing services, individuals will accept SARS-CoV-2 Ag RDT, symptomatic and asymptomatic SARS-CoV-2 infections will be diagnosed, and individuals diagnosed with SARS-CoV-2 will be linked to care and treatment services. This will lead to isolation of SARS-CoV-2 infected individuals, quarantining of contacts, and medical treatment for those requiring it.
Study Design This will be a community-based cross-sectional study. The study will be conducted among the population of Kiambu County, central Kenya, attending specific high-volume community venues identified as possible points of community-based transmission.
These high-volume community venues will be:
Venues identified by individuals diagnosed with SARS-CoV-2 infection in a subset of CCA-supported facilities in Kiambu County. As part of the CCA questionnaire, participants will be asked to identify crowded places the participants had been to in the 10 days prior to their positive SARS-CoV-2 test. This will provide an opportunity for the staff to identify market places, places of worship, schools, or other venues where SARS-CoV-2 transmission is likely to occur in the communities. In this study, no testing activities will be conducted in health facilities.
Venues identified in collaboration with the department of public health and the Coronavirus-19 response team in the county that may act as transmission hotspots.
Using both approaches above, the investigators will identify venues in Kiambu county where a large number of people congregate to propose mass testing.
Variant surveillance population Individuals who test positive with SARS-Cov-2 Ag-RDT and those who test negative but with symptoms of Coronavirus-19 will be asked to provide a second sample for confirmatory PCR testing and whole genome sequencing for variant surveillance. The participants will be taken care of as Coronavirus-19 cases as the participant wait for the PCR result. Based on the national guidelines on management of Coronavirus-19 in Kenya, a person who meets the clinical and epidemiological criteria is a suspected case of SARS-CoV-2. The participant will be assessed and based on the severity of their symptoms the participant will either be referred to a treatment centre where symptoms will be managed. If the person has mild symptoms he will be referred for home based care. The study team will transport those who need to be hospitalized to the hospital. Kiambu county currently has 5 treatment centres which also act as isolation centres. While secondary sample collection is part of routine national surveillance, because these results will be used for research purposes, the investigators will only perform this study activity for those who voluntarily agree to this study through administration of a written informed consent. The second sample will be taken at the community venue for those who will have given written consent/assent and transported to the testing laboratory in accordance with the standard operating procedures.
Inclusion criteria for variant surveillance:
Venue attendee with a positive result to SARS-Cov-2 Ag-RDT Venue attendee with a negative Ag-RDT, but with Coronavirus-19 symptoms Provide written informed consent to collect a second sample Community mobilization and recruitment This section describes activities conducted by Kiambu County Coronavirus-19 response team ahead of the start of study activities.
Mobilizing the community to ensure a high response rate is a priority for successful study implementation the Kiambu County Coronavirus-19 response team will be engaged from the initial stages to ensure that the security coordination mechanisms are well informed.
Before the mass testing, meetings will be held with the community leaders to explain the study and have the opportunity to discuss potential problems and concerns, including preventing dissemination of false information. These meetings will be coordinated by the public health department in the county in strong collaboration with the EGPAF team. Depending on the venue, key stakeholders may include social workers, community health volunteers, local community leaders (chiefs, sub chiefs), members of the county and sub- county health management teams, including those from the public health department, county Coronavirus-19 response manager, county education department, school principals, religious leaders, among others. Ongoing dialogue with these stakeholders will be important to maintain community engagement before and during the study implementation.
A few days before the start of testing campaign, community health volunteers will visit the selected high attendance venues and a poster announcing the community testing activity will be distributed for display in the venue prior to the scheduled testing intervention.
Trained community health volunteers and mobilizers will present to the venue on the pre-agreed day(s) to announce the actual testing day and mobilize the community. Available channels like community, Facebook, and other social media will also be used to mobilize the community. Through church leaders and association of pastors, messages about the testing will be posted on church websites where available. Megaphones and caravans may also be used for community mobilization as deemed appropriate.
Data Collection on the day of testing, individuals accessing the venue will be informed of the SARS-CoV-2 testing taking place and asked if the participants are willing to be tested. An anonymous screening log will be completed for all individuals offered testing, which will include age, sex, whether testing was accepted or not, and any reported reasons for choosing not to test. This will allow capture of a brief description of the population at each venue and documentation of the testing refusal rate.
For those who opt in for testing, the MoH staff will provide routine information on the test procedure before performing the test (see section on testing procedure). During the consenting process, information about the study objectives and procedures will be provided and the client will be able to ask questions. Those who agree will then undergo a 2- to 5-minutes interview. The data obtained from the interview will be recorded in the data collection tool and later entered into the study database.
For individuals tested positive and those negative referred for PCR because of Coronavirus-19 symptoms, the investigators will also collect information on their final PCR result, and the result of their sequencing test after obtaining from them a written informed consent.
PCR/whole genome sequencing (WGS) surveillance:
Kenya Medical Research Institute-Wellcome Trust Research Laboratory in Kilifi is currently the laboratory tasked by the Ministry of Health with SARS-CoV-2 genome sequencing in Kenya. The laboratory operates in compliance with Good Clinical Laboratory Practice (GCLP) standards. For this study, the Coronavirus-19 sequencing sample manifest form (QMS-F238- Annex 5) will be completed with all the required information and sent together with the swabs to Kenya Medical Research Institute-Wellcome Trust Research Laboratory. Laboratory staff will communicate results to the study team using the unique identifiers described above; the study team will update the study database.
Costs will be estimated from a health systems perspective using a micro-costing method, combining top-down and bottom-up approaches to obtain resource use and costs per line item. All project costs will be converted to 2022 U.S. dollars (US$) using the prevailing exchange rate and adjusted to inflation using the U.S. consumer price index if needed.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 2 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- The study population will be composed of all persons attending the selected venue where testing is offered on the day of the testing campaign, including all ages > 2 years regardless of presence of coronavirus-19 symptoms. This population will include people from different economic and social backgrounds.
Key inclusion criteria (3 listed)
- Age > 2 years
- Agrees to Undergo testing with SARS-CoV-2-Ag RDT on the day of testing campaign
- Ability and willingness to provide written consent/assent for participation in an interview following the test
Key exclusion criteria (1 listed)
- 1. Positive SARS-CoV-2 test done 1 to 14 days before the current testing campaign
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Rapid Antigen TestingCommunity testing for SARS-COV-2 using rapid Antigen test | Diagnostic test | – |
Primary outcome
SARS-CoV-2 case detection rate
Time frame: This will be done in a period of 4 months of study enrolment
Will determine the proportion of SARS-CoV-2 infections detected per 100 individuals tested) in high volume community venues using SARS-CoV-2 Ag-RDT, overall and disaggregated by venue type.
5 secondary outcomes
Proportion testing positive across the cascade
Time frame: 4 months
Positive cases by type
Time frame: 4months
Factors
Time frame: 4 months
SARS-COV-2 variants
Time frame: 4 months
Costing
Time frame: 4months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Apr 2023.
- Derived from this study: PubMed 39591654Masaba R, Siamba S, Hoffman HJ, Osire E, Kimani N, Kwasa M, Songane M, Denoeud-Ndam L. A Cross-Sectional Study of the Use of Antigen Rapid Diagnostic Tests for Community Identification of SARS-CoV-2 in Kenya. Am J Trop Med Hyg. 2024 Nov 26;112(4_Suppl):17-25. doi: 10.4269/ajtmh.23-0756. Print 2025 Apr 1.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Severe Acute Respiratory Syndrome Coronavirus 2 Infection, run by Elizabeth Glaser Pediatric AIDS Foundation at 1 site in Kenya.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 19 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Kenya. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
SARS-CoV-2 case detection rate (time frame: This will be done in a period of 4 months of study enrolment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05458557, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Apr 2023.