Clinical trial Recruiting at 1 site Observational Ages 6 and up

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.

More Respiratory Syncytial Virus (RSV) trials

Quick facts

Study typeObservational
Ages6 Years and up
SexAll
Enrollment910 (estimated)
SponsorFiji National University
Academic / other
Locations1 site (Suva, Central)
StatusRecruiting
StartedOctober 23, 2025
Main results expectedDecember 31, 2025
Study endsDecember 31, 2028
Registry record updatedDecember 1, 2025
Trial IDNCT07229677 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.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.