Tracking mosquito-borne and other emerging virus infections in Fiji
Official title: The AEVI-Fiji Cohort Study: a Longitudinal Study Assessing the Transmission Risk and Dynamics of Mosquito-borne and Respiratory Viruses in Fiji.
Run by Fiji National University · NCT07229677 · Data updated 2026-11-12
This project will follow people aged 6 and older who live in Fiji's Central Division to see how often mosquito-borne and respiratory viruses infect them over time.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 6 Years and up |
| Sex | All |
| Enrollment | 910 (estimated) |
| Sponsor | Fiji National University Academic / other |
| Locations | 1 site (Suva, Central) |
| Status | Recruiting |
| Started | October 23, 2025 |
| Main results expected | December 31, 2025 |
| Study ends | December 31, 2028 |
| Registry record updated | December 1, 2025 |
| Trial ID | NCT07229677 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are residents of Fiji's Central Division aged 6 years or older who have lived in a selected household for at least six months and can provide informed consent.
✕Probably not a fit
People who are pregnant, homeless, legally unable to consent, under psychiatric care or institutionalized, or otherwise excluded by the protocol will not be eligible and are unlikely to receive direct benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a longitudinal household cohort in Fiji's Central Division that enrolls residents aged 6 years and older and follows them over time to measure exposure to arboviruses (like dengue, Zika, chikungunya) and respiratory viruses (including influenza and SARS-CoV-2). Participants provide health questionnaires and biological samples at set visits so researchers can measure antibodies and detect infections. The work is coordinated locally by Fiji National University with laboratory and analytic collaboration from regional and international partners. Results will map seroprevalence, changes in immunity, and patterns of virus circulation across seasons and years.
Why it matters
Potential benefit: If successful, this work could help public health officials detect outbreaks earlier and target prevention measures like mosquito control or vaccination more effectively.
How similar studies have gone: Previous seroprevalence and longitudinal cohort studies of dengue, Zika, chikungunya, and SARS-CoV-2 have successfully identified transmission patterns and informed public health responses.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Individuals aged 6 years and older who reside in the Central Division of Fiji * Have lived in the selected household for at least six months at the time of enrollment Exclusion Criteria: * Pregnant women; * Women in labor, or breastfeeding mothers; * Individuals deprived of liberty by judicial or administrative decision; * Individuals under psychiatric care or admitted to a health or social care facility for purposes other than participation in the study; * Adults under legal protection or unable to provide informed consent; * Homeless individuals; * Individuals with severe disabilities preventing mobility; * Individuals unable to understand or complete the study questionnaire
Where it's running
-
Fiji National University
Suva, Central, Fiji Recruiting
Study contacts
- Principal investigator: Donald Wilson, MBBS, PhD-Epidemiology — Fiji National University
- Study coordinator: Isireli Koroituku, Masters Infectious Diseases
- Email: isireli.koroituku@fnu.ac.fj
- Phone: +679 9090729
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Passive RSV antibody to protect Aboriginal and Torres Strait Islander infants
This trial tests whether giving a single shot of the RSV antibody nirsevimab to Aboriginal and Torres Strait Islander infants around 6 months old can reduce RSV infections in the first year of life.
-
Characterizing T-cell responses to arbovirus infections using ELISpot tests
This project will test whether ELISpot blood assays can detect T-cell immune responses in adults with suspected arbovirus infections.
-
Preparedness through community respiratory virus testing and engagement
This program will offer community members regular testing for respiratory viruses like COVID-19, flu, and RSV and invite some people to join longer-term monitoring and household transmission follow-up.
-
How viral infections affect people with chronic lung disease
This study will test if respiratory viruses trigger flare-ups and change immune responses in adults with COPD or bronchiectasis.
-
Deuremidevir hydrobromide treatment for RSV in infants and young children
This trial tests whether deuremidevir hydrobromide, given by weight three times daily for five days, helps infants and young children (1–36 months) with confirmed RSV recover faster or have milder symptoms than a placebo.
-
RSV strains and illness burden in Vietnamese adults aged 60 and older
This project will test how common RSV is and which strains and severity patterns occur in people aged 60+ who are hospitalized with acute respiratory illness or worsening heart/lung disease.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.