Evaluating the Impact of Computer-assisted X-ray Diagnosis and Other Triage Tools to Optimise Xpert Orientated Community-based Active Case Finding for TB and COVID-19
NCT ID: NCT05220163
Last Updated: 2025-09-25
Study Results
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Basic Information
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ACTIVE_NOT_RECRUITING
NA
26200 participants
INTERVENTIONAL
2022-02-23
2025-12-31
Brief Summary
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Detailed Description
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Detecting cases in the community, however, has been restricted by the lack of sensitive and user-friendly Point-of-Care (POC) diagnostic tools. To address this unmet need, in 2013 the investigators planned a programme of activities (sequential interlinked studies) with the overarching aim of optimising a model for Xpert-related community-based active case finding (ACF) for TB (XACT). By 2017, through the EDCTP-funded XACT-I study, the investigators solved the impasse of rapid POC diagnosis by showing that molecular Xpert-based community-based screening was effective in identifying missing TB cases in the peri-urban 'slums' of Cape Town and Harare using a mini-truck with a generator. However, such an approach was neither broadly affordable nor scalable. The investigators therefore derived a scalable model using portable battery-operated Xpert Edge installed within a low-cost (\< US$) 15 000 Nissan panel van manned by two health care workers (thus making the ACF model affordable and scalable). This completed study, XACT-II, screened over 5 000 participants in the community. The model worked well and was more effective than smear microscopy. Based on these successes, and to translate the XACT concept into policy, the Wellcome Trust and UK MRC has funded the XACT-III study. Currently commenced, XACT-III was initiated as a multi-country demonstration project in four sub-Saharan African countries.
More recently, there have been rapid advances in the development of triage testing for TB, which refers to screening tests that are generally applied in a community-based setting (either at individual community or primary care clinic level). These tests have very high sensitivity (\>95%) but modest specificity (\>70%) as defined by TB-specific target product profiles. A forerunner TB-orientated triage test is computer-assisted x-ray diagnosis (CAD). This entails using artificial intelligence-enabled software to read a digital x-ray and produce a probability of TB within seconds. Recent data suggest that CAD performs on par with experienced radiologists to identify potential TB cases, hereby reducing the frequency at which Xpert tests are requested and helps to focus limited resources on the relevant cases. Although these data appear promising, the feasibility of this strategy in a pragmatic field setting has not been extensively tested. There are several other unanswered questions. Is the strategy of CAD combined with Xpert cost-effective and can it reduce Xpert usage without missing an unacceptable number of TB cases? The investigators will therefore determine the utility of CAD as a triage tool to further optimise the XACT model.
The COVID-19 pandemic, due to SARS-CoV-2, has ravaged African peri-urban communities where TB is also common. Symptoms of COVID-19 and TB overlap, and limited affordability, as well as the stigma associated with both diseases, severely limits testing. Data are now urgently needed about the feasibility of co-screening and testing for TB and COVID-19. The utility of such an approach, if any, has not been studied in African communities. As Xpert POC TB testing and x-rays for CAD will be performed in the proposed study, it affords a unique and easy opportunity to seamlessly screen for both diseases when appropriate.
Other nascent screening technologies are rapidly emerging for TB and COVID-19, including urine- and blood-based triage tests. XACT-19 provides a unique opportunity to collect the relevant samples and test new technologies in a pragmatic community-based setting.
In summary, the XACT-19 study results will have substantial implications for public health policy and practice and will likely define a new standard for community-based ACF for TB, and potentially COVID-19 in tandem.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SCREENING
NONE
Study Groups
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CAD + POC Xpert
CAD followed by Xpert in CAD-positive participants (performed at POC) employing a low-cost panel van that is staffed by three health care workers. CAD-negative participants will be followed up, while CAD-positive participants will be offered POC Xpert. Xpert-positive participants will be referred for TB treatment initiation, while Xpert-negative (but CAD-positive) participants will undergo a clinical review. Thus, the active case finding (ACF) interventional package is one of CAD + POC Xpert (only in CAD positive participants).
CAD
It is an artificial intelligence (AI) system for detection of TB on CXR images. The system input is a frontal CXR, and the outputs are 1) a heatmap indicating suspicious regions on the image; and 2) a score (0-100) which implies the likelihood that the x-ray image shows TB.
Xpert
A novel diagnostic for active case finding (GeneXpert MTB/RIF) for TB on sputum collected and performed at POC in a mobile van.
POC Xpert only
Participants who are Xpert-positive will be referred for TB treatment initiation while Xpert-negative participants will be followed up. Thus, the active case finding (ACF) standard of care package is POC Xpert.
Xpert
A novel diagnostic for active case finding (GeneXpert MTB/RIF) for TB on sputum collected and performed at POC in a mobile van.
Interventions
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CAD
It is an artificial intelligence (AI) system for detection of TB on CXR images. The system input is a frontal CXR, and the outputs are 1) a heatmap indicating suspicious regions on the image; and 2) a score (0-100) which implies the likelihood that the x-ray image shows TB.
Xpert
A novel diagnostic for active case finding (GeneXpert MTB/RIF) for TB on sputum collected and performed at POC in a mobile van.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Provision of informed consent.
* Participant 18 years or above.
* HIV-positive or negative participants will be included.
Exclusion Criteria
* Participants who have completed TB treatment in the last two months, or who have self-presented to their local TB clinic and are currently being worked up for suspected TB.
* Participants already diagnosed with active TB on treatment.
* Participants unable to commit to at least a two-month follow-up.
* Female participants who are pregnant or who refuse a urine pregnancy test.
* Participants in the community who cannot access healthcare due to severe ill health or lack of access to the local clinic.
18 Years
ALL
Yes
Sponsors
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European and Developing Countries Clinical Trials Partnership (EDCTP)
OTHER_GOV
Zambart
OTHER
Biomedical Research and Training Institute
OTHER
Ospedale San Raffaele
OTHER
Radboud University Medical Center
OTHER
Foundation for Innovative New Diagnostics, Switzerland
OTHER
University of Stellenbosch
OTHER
University of Cape Town
OTHER
Responsible Party
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Keertan Dheda
Professor
Principal Investigators
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Keertan Dheda, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Cape Town
Locations
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University of Cape Town
Cape Town, Western Cape, South Africa
Helen Ayles
Lusaka, , Zambia
Junior Mutsvangwa
Harare, , Zimbabwe
Countries
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Other Identifiers
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XACT-19
Identifier Type: -
Identifier Source: org_study_id
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