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Transmission of Coronavirus Disease 2019 (COVID19) in Crowded Environments

Transmission of COVID19 in Crowded Environments

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05119348
Acronym
TRACE
Enrollment
245
Registered
2021-11-15
Start date
2020-09-14
Completion date
2021-10-21
Last updated
2024-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, Sars-CoV-2 Infection

Brief summary

South Africa recorded it's first coronavirus disease 2019 (COVID19) case on March 5, 2020. In response to the COVID19 outbreak World Health Organisation recommendations, South Africa implemented non-pharmaceutical recommendations. The major risk mitigation factors recommended by World Health Organisation and others - physical distancing and hygiene - are extremely difficult to implement in much of Africa. The investigators will conduct a randomised controlled trial to investigate the effect of an infection mitigation intervention to assess the effect on household transmission of severe acute respiratory syndrome (SARS) coronavirus (CoV) 2 in household settings with an index patient diagnosed SARS-CoV-2 positive.

Detailed description

The major risk mitigation factors recommended by World Health Organisation and others - physical distancing and hygiene - are extremely difficult to implement in much of Africa. Newly diagnosed SARS-CoV-2 index patients will be identified and recruited from a mobile clinic and local community clinics conducting SARS-CoV-2 testing. Index cases and their households will be invited to enroll. The study design is a type 2 hybrid cluster (household) randomised controlled trial, with outcomes assessed on index patients and their household contacts. 120 consecutively newly diagnosed index patients (GeneXpert severe acute respiratory syndrome coronavirus 2 PCR) and up to 6- 8 household contacts will be invited to participate in the trial as part of the prospective observational study evaluating transmission and symptoms. After completing consent, households will be randomised in a 1:1 ratio in blocks of 10 (60 households per group). Klipfontein is a resource-limited, densely populated, high HIV/tuberculosis disease burden areas in Cape Town. Newly diagnosed COVID19 cases will be identified from two sources: screening conducted in Desmond Tutu Health Foundation mobile screening units and local public sector clinics working closely with Desmond Tutu Health Foundation. Consecutive cases (n=120 cases and households) will be invited to participate in the randomised trial and prospective longitudinal follow up of up to 6- 8 household contacts. The contacts will be followed up after informed consent to SARS-CoV-2 screening, symptomatic questionnaires weekly up to 1 month. After enrolment, the household will be randomised to the infection mitigation intervention or enhanced usual care messaging. Baseline demographic, household characteristics questionnaire will be administered, and each household occupant invited to participate. Following consent procedures, household contacts (HHC) will be screened at baseline and weekly for 4 weeks for evidence of COVID19 infection. Specifically, the research team will conduct SARS-CoV-2 GeneXpert PCR testing and antibody serology. They will collate self- administered daily symptom checks on a weekly basis. The investigators will recruit 120 households over 1-11 months. The investigators will initiate a prospective longitudinal follow up of the household contacts of each case for 4 weeks in each case. The investigators will calculate proportion of SARS-CoV-2 transmission from index cases in each household over 4- week period and describe the proportion of symptomatic and asymptomatic SARS-CoV-2 infection in a high density, low resourced community. Investigate the impact of the infection mitigation intervention by comparing incidence in households randomised to intervention versus standard of care. Secondary outcomes for the trial will include clinical outcomes (hospitalisations, death), linkages to care for people, psychosocial functioning, and stigma.

Interventions

OTHERSTOPCOV

Fieldworkers delivered an infection mitigation intervention which consisted of personal protective equipment and messaging on managing COVID19 and reducing onward transmission of SARS-CoV-2 infection.

Sponsors

Amsterdam Institute for Global Health and Development
CollaboratorOTHER
European and Developing Countries Clinical Trials Partnership (EDCTP)
CollaboratorOTHER_GOV
University of Cape Town
CollaboratorOTHER
Desmond Tutu HIV Foundation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Masking description

The investigators were not made aware of participants study condition.

Intervention model description

The study design is a type 2 hybrid cluster (household) randomised controlled trial, with outcomes assessed on index patients and their household contacts. After completing consent, 120 households will be randomised in a 1:1 ratio (60 per arm).

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* recently diagnosed SARS-CoV-2 positive * Individual \>12 years * Able to give assent if \<18 years with parental/guardian consent * Able to give consent\> 18 years * Self-isolating at home at the time of COVID diagnosis

Exclusion criteria

* \<12 years * Unable to give consent

Design outcomes

Primary

MeasureTime frameDescription
SARS-CoV-2 Infection4 weeksNumber of participants with positive SARS-CoV-2 PCR result

Secondary

MeasureTime frameDescription
COVID19 Symptoms4 weeksNumber of participants with SARS-CoV-2 serology antibody positive result

Countries

South Africa

Participant flow

Participants by arm

ArmCount
Stop Coronavirus (STOPCOV)
A fieldworker will deliver the STOPCOV pack and personal protective equipment at baseline. The fieldworker will communicate with intervention households daily, delivering STOPCOV hygiene information. STOPCOV: Fieldworkers delivered an infection mitigation intervention which consisted of personal protective equipment and messaging on managing COVID19 and reducing onward transmission of SARS-CoV-2 infection.
137
Control
Participants received no additional messaging about managing COVID19 in the household.
108
Total245

Baseline characteristics

CharacteristicControlTotalStop Coronavirus (STOPCOV)
Age, Continuous39.9 years
STANDARD_DEVIATION 17.1
39.1 years
STANDARD_DEVIATION 16.8
38.4 years
STANDARD_DEVIATION 16.6
Race/Ethnicity, Customized
Race
Black
22 Participants91 Participants69 Participants
Race/Ethnicity, Customized
Race
Coloured
82 Participants150 Participants68 Participants
Race/Ethnicity, Customized
Race
Indian
3 Participants3 Participants0 Participants
Race/Ethnicity, Customized
Race
Prefer not to say
1 Participants1 Participants0 Participants
Region of Enrollment
South Africa
108 participants245 participants137 participants
Sex: Female, Male
Female
60 Participants139 Participants79 Participants
Sex: Female, Male
Male
48 Participants106 Participants58 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1370 / 108
other
Total, other adverse events
15 / 1374 / 108
serious
Total, serious adverse events
0 / 1370 / 108

Outcome results

Primary

SARS-CoV-2 Infection

Number of participants with positive SARS-CoV-2 PCR result

Time frame: 4 weeks

Population: Number of participants where there was a change observed in their negative to a positive SARS-CoV-2 PCR result

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Stop Coronavirus (STOPCOV)SARS-CoV-2 Infection4 Participants
ControlSARS-CoV-2 Infection2 Participants
Secondary

COVID19 Symptoms

Number of participants with SARS-CoV-2 serology antibody positive result

Time frame: 4 weeks

Population: Number of participants where there was a change observed in their negative to a positive SARS-CoV-2 serology result

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Stop Coronavirus (STOPCOV)COVID19 Symptoms11 Participants
ControlCOVID19 Symptoms9 Participants

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026