University-Based Chagas Testing in Salta Province, Argentina
NCT ID: NCT07033325
Last Updated: 2025-06-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
5000 participants
OBSERVATIONAL
2024-09-11
2026-02-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
* What is the seroprevalence and geographic distribution of T. cruzi infection in UNSa students?
* Can voluntary point-of-care tests performed at university serve as an effective opportunity for timely diagnosis and linkage to care for Chagas disease?
Participants will:
1. Be offered a RDTs (WL Check Chagas, Wiener Lab) during their regular activities in the university.
2. If RDT is positive, be referred to the health system for confirmatory testing and treatment.
3. Receive follow-up support by trained staff via phone. A subgroup of RDT-negative students will have serum samples preserved and analyzed later via ELISA to verify RDT accuracy.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Chagas Disease Diagnostic - Inconclusive Serology
NCT00511589
Management of Soil-transmitted Helminthiasis and Strongyloidiasis
NCT01308268
Prospective Evaluation of the Specificity of Serological Tests for Human African Trypanosomiasis
NCT05466630
Urine Albendazole Levels for Coverage Assessment
NCT04041427
Diagnostic Tools for Human African Trypanosomiasis Elimination and Clinical Trials: WP3 Post Elimination Monitoring
NCT04099628
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Despite the availability of effective therapy, access to diagnosis and treatment remains limited due to both health system and patient-related barriers. The reported prevalence in Salta province is high: around 5% in blood banks and up to 8% among pregnant women.
The Universidad Nacional de Salta (UNSa), with nine campuses across the province, requires all incoming students to complete a medical check-up. This project leverages that existing requirement to offer rapid diagnostic testing (RDT) for T. cruzi, aiming to identify cases early, link positive individuals to care, and indirectly reach affected families.
The study will be implemented by a multidisciplinary team including researchers in medicine, biology, biochemistry, anthropology, and public health, with institutional support from the Universidad Nacional de Salta, Fundación Mundo Sano, and Salta's Ministry of Public Health.
Objectives
Primary Objectives:
1. Increase access to T. cruzi diagnosis and etiological treatment for chronic infections among university students.
2. Prevent congenital transmission of Chagas disease.
Secondary Objectives:
1. Evaluate the use of RDTs in a point-of-care (POC) approach.
2. Determine T. cruzi seroprevalence and geographic distribution among UNSa students.
3. Promote community awareness and knowledge about Chagas disease.
4. Support public health treatment efforts.
5. Assess treatment adherence and safety.
6. Facilitate screening of family members of positive cases.
7. Explore students' knowledge, attitudes, and practices (KAP) regarding Chagas disease.
Methodology
Design:
Implementation research with mixed methods (quantitative and qualitative components).
Study population All incoming students at UNSa in 2024, across all campuses, regardless of age or gender. In addition, other members of the university community (including teachers, administrative staff, and support personnel) who voluntarily choose to participate.
Sites and Estimated Participants:
In 2023, approximately 23,500 students pre-registered, with \~8,000 beginning courses. Campuses are located in Salta Capital, Tartagal, Orán, Metán, Cafayate, Rosario de la Frontera, Santa Victoria Este, San Antonio de los Cobres, and Joaquín V. González. The estimated number of participants is \~5,000.
Procedures
1. Enrollment:
The Chagas test is offered on a voluntary basis. At the Salta Capital campus, all first-year students are offered the test during their routine medical examination at UNSa, and other members of the university community may also receive the test whenever they visit the university health office. In the regional campuses, testing is carried out through short, intensive Chagas screening campaigns held in university facilities for several weeks during the year, during which any staff or students may participate. Pre-test information is provided, and participants give informed consent.
2. Testing:
Chagas RDT (WL Check Chagas, Wiener Lab) is performed via fingerstick.
3. Results:
Participants are informed of results via phone in case of negative results and on-site in case of positive results. Positive cases are referred to the public health system for confirmatory testing (HAI and ELISA) and evaluation (ECG, clinical assessment), and are also contacted by Mundo Sano staff to support follow-up and answer questions.
4. Epidemiological Survey:
All participants complete a Knowledge, Attitudes, and Practices (KAP) survey, either through an online questionnaire accessed via a QR code or using a printed version when needed.
5. Family and Entomological Surveillance:
Public health authorities will follow up with family members of positive cases and conduct home vector inspections when applicable.
6. Evaluation of the Diagnostic Test A validation study will be conducted with 100 negative students to compare RDT results with ELISA testing.
7. Treatment Protocol The public health system guarantees confirmation, notification, free drug provision, and medical follow-up. Drugs used: Benznidazole or Nifurtimox.
Treatment adherence, side effects, and outcomes are monitored. Mundo Sano offer telephone or WhatsApp support during treatment.
Data Analysis The analysis will include both quantitative and qualitative components to comprehensively assess the implementation and outcomes of the study.
Quantitative Analysis Data will be collected on the following variables: 1)Demographics: age, sex, current residence, and birthplace. 2) Epidemiological history: including maternal Chagas status, history of blood transfusions, and contact with Chagas vectors. 3)Diagnostic results: including the result of the rapid diagnostic test (RDT) and confirmatory testing (HAI and ELISA). 4) Clinical outcomes: such as treatment status, adherence, adverse effects, and treatment completion among positive cases. 5) Geographic data: for spatial analysis and visualization of case distribution using Geographic Information Systems (GIS).
Descriptive statistics will be used to summarize both continuous and categorical variables. Comparative analyses will be performed using t-tests or Mann-Whitney U tests for continuous variables, and chi-square tests for categorical variables. Associations between key variables will be explored through bivariate and multivariate logistic regression analyses. Geographic distribution of positive cases will be represented using GIS mapping to identify regional patterns of T. cruzi infection within the province.
Data will be managed and analyzed using Microsoft Excel, R statistics, and EPIDAT 4.2.
Qualitative Analysis Qualitative data will be collected through: 1) Pre- and post-treatment Knowledge, Attitudes, and Practices (KAP) surveys. 2) Observations of selected medical consultations (with participant consent). 3) In-depth interviews and extended case studies with a subset of students diagnosed positive. 4) Focus group discussions to explore experiences of participants diagnosed and treated for Chagas. 5) An evaluation of the patient experience with the public health system following diagnosis and referral.
These qualitative methods will provide insight into participants' perceptions of the disease, barriers to care, adherence to treatment, and the overall acceptability of the intervention. Data will be coded and thematically analyzed to identify key patterns and inform future implementation strategies.
Ethical Considerations Approval from Hospital Señor del Milagro and Salta´s Province Bioethics Committee. Informed consent is mandatory. Participation is voluntary and free of charge. Confidentiality is strictly maintained. Results are not a barrier to university entry or employment (per Argentina's National Chagas Law No. 26.281).
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
CROSS_SECTIONAL
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Rapid diagnostic test (RDT) for Trypanosoma cruzi infection.
Rapid diagnostic tests (RDTs) for the detection of Trypanosoma cruzi infection are performed in university facilities, outside of a clinical care setting, using a point-of-care approach. The study population includes adult male and female participants from the university community. This intervention differs from most existing strategies that target exclusively women of reproductive age and/or newborns to control vertical transmission; instead, it focuses on broader population-based screening and linkage to care for chronic infections.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Aged 18 years or older.
* Of any sex or gender.
* Able and willing to provide informed consent.
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Universidad Nacional de Salta
OTHER
Mundo Sano Foundation
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Adriana Echazu
Project Director
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Adriana Echazu, PhD
Role: STUDY_DIRECTOR
Mundo Sano Foundation
Ruben O Cimino, PhD
Role: STUDY_CHAIR
Instituto de Investigaciones de Enfermedades Tropicales, Univeridad Nacional de Salta
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Universidad Nacional de Salta
Orán, Salta Province, Argentina
Universidad Nacional de Salta
Salta, , Argentina
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Lopez-Albizu C, Danesi E, Piorno P, Fernandez M, Garcia Campos F, Scollo K, Crudo F. Rapid Diagnostic Tests for Trypanosoma cruzi Infection: Field Evaluation of Two Registered Kits in a Region of Endemicity and a Region of Nonendemicity in Argentina. J Clin Microbiol. 2020 Nov 18;58(12):e01140-20. doi: 10.1128/JCM.01140-20. Print 2020 Nov 18.
OPS. Organización Panamericana de la Salud. Guía para el diagnóstico y el tratamiento de la enfermedad de Chagas. Washington, D.C. OPS; 2018. 2018. 1-172 p.
Ministerio de Salud de la Nación. Enfermedad de Chagas. Guía para la atención al paciente infectado con Trypanosoma cruzi. 2018. 96 p.
WHO Expert Committee. Control of Chagas disease. World Health Organ Tech Rep Ser. 2002;905:i-vi, 1-109, back cover.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
5/2024-SCRTI-UNSa
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.