NCT06859619

Brief Summary

Zoonoses and arboviroses refer to a group of diseases transmitted from animals to humans, either directly or indirectly (via mosquitoes, ticks or contact with contaminated environments). Most of these diseases are found in certain tropical zones, but global warming and increased international trade are modifying their geographical distribution, with a gradual trend towards temperate regions. A number of these pathogens have already been detected in Occitania, including dengue fever, West Nile, leishmaniasis and Q fever. Given the region's high mosquito population and favorable climatic conditions, other zoonoses have a strong potential to appear in the region, or may already be circulating at a low level. The study focuses on 18 pathogens selected for their potential to emerge and establish themselves in the Occitanie region: Leishmaniasis, Leptospirosis, Brucellosis, Q fever, Rickettsiosis, Tularemia, Psittacosis, Lyme disease, Tick-borne encephalitis, Hantavirus, Hepatitis E virus, Dengue virus, Zika virus, Chikungunya virus, West-Nile virus, Usutu virus, Toscana virus, Crimean-Congo haemorrhagic fever virus. The aim of the study is to find out whether patients have antibodies against these infectious agents, which would indicate that they have been exposed to them in the past, even in the absence of symptoms. Describing the circulation of these pathogens will enable to implement appropriate public health measures to avoid the risk of epidemics (mosquito control, informing professionals, etc.), as well as to assess the risk incurred in the workplace and have this risk recognized by the healthcare system.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
183

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 27, 2025

Completed
4 days until next milestone

Study Start

First participant enrolled

March 3, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 5, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 3, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 3, 2025

Completed
Last Updated

March 5, 2025

Status Verified

February 1, 2025

Enrollment Period

7 months

First QC Date

February 27, 2025

Last Update Submit

February 27, 2025

Conditions

Keywords

Leishmaniasis,LeptospirosisBrucellosisZika virusQ fever, RickettsiosisLyme diseaseTick-borne encephalitiHantavirusHepatitis E virusDengue virusChikungunya virusWest-Nile virusUsutu virusToscana virusTularemiaPsittacosisCrimean-Congo haemorrhagic fever virusepidemiology

Outcome Measures

Primary Outcomes (18)

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies). Leishmaniasis,

    prevalence (in percentage) of pathogen IgG positivity against : Leishmaniasis,

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Leptospirosis,

    prevalence of pathogen IgG positivity against : Leptospirosis,

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Brucellosis

    prevalence of pathogen IgG positivity against : Brucellosis

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Q fever

    prevalence of pathogen IgG positivity against : Q fever

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Rickettsiosis

    prevalence of pathogen IgG positivity against : Rickettsiosis,

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Tularemia

    prevalence of pathogen IgG positivity against : Tularemia

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Psittacosis

    prevalence of pathogen IgG positivity against : Psittacosis

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Lyme disease,

    prevalence of pathogen IgG positivity against : Lyme disease,

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Tick-borne encephalitis

    prevalence of pathogen IgG positivity against : Tick-borne encephalitis

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Hantavirus

    prevalence of pathogen IgG positivity against : Hantavirus

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies). Hepatitis E virus

    prevalence of pathogen IgG positivity against : Hepatitis E virus

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Dengue virus

    prevalence of pathogen IgG positivity against : Dengue virus

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies). Zika virus

    prevalence of pathogen IgG positivity against : Zika virus

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Chikungunya virus

    prevalence of pathogen IgG positivity against : Chikungunya virus

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies). West-Nile virus,

    prevalence of pathogen IgG positivity against : West-Nile virus,

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies). usutu virus

    prevalence of pathogen IgG positivity against : Usutu virus

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Toscana virus

    prevalence of pathogen IgG positivity against : Toscana virus

    Baseline

  • Estimate seroprevalences of the zoonoses in populations exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies).Crimean-Congo haemorrhagic fever virus.

    prevalence of pathogen IgG positivity against : Crimean-Congo haemorrhagic fever virus.

    Baseline

Secondary Outcomes (23)

  • Determine the factors associated with seropositivity to these diseases. socio-demographic criteria

    Baseline

  • Determine the factors associated with seropositivity to these diseases. travel to endemic areas

    Baseline

  • Determine the factors associated with seropositivity to these diseases. occupational exposure

    Baseline

  • Determine the factors associated with seropositivity to these diseases. exposure in private activities

    Baseline

  • Determine the factors associated with seropositivity to these diseases. use of mosquito protection

    Baseline

  • +18 more secondary outcomes

Study Arms (1)

City of Montpellier employees working at the Zoo, the Ecolothèque and the Green Spaces Department

EXPERIMENTAL

City of Montpellier employees working at the Zoo, Ecolotheque or green spaces exposed to wildlife by zoo staff and to various vectors (ticks, mosquitoes, sandflies) in the Occitanie region

Other: Peripheral venous blood sample

Interventions

Peripheral venous blood sampling for IgG serology against leishmaniasis, leptospirosis, brucellosis, Q fever, rickettsiosis, tularemia, psittacosis, Lyme disease, tick-borne encephalitis, hantavirus, hepatitis E virus, dengue virus, Zika virus, Chikungunya virus, West Nile virus, Usutu virus, Toscana virus, Crimean-Congo hemorrhagic fever virus.

City of Montpellier employees working at the Zoo, the Ecolothèque and the Green Spaces Department

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age 18 or over
  • Consultant in an infectious diseases department
  • Have given written consent to participate in the study
  • Working for the City or Metropolis of Montpellier in the Zoo, Espaces Vert or Ecolothèque departments.

You may not qualify if:

  • \- Pregnant and breast-feeding women
  • Persons benefiting from legal protection measures (guardianship, curatorship, safeguard of justice)
  • Participants who are not fluent in French and who do not have a support person capable of reading French.
  • Persons unable to express their consent.
  • Persons not affiliated to a social security scheme or not benefiting from such a scheme.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Of Montpellier

Montpellier, herault, 34295, France

Location

MeSH Terms

Conditions

LeishmaniasisLeptospirosisBrucellosisQ FeverRickettsia InfectionsTularemiaPsittacosisLyme DiseaseEncephalitis, Tick-BorneHepatitis EZika Virus InfectionChikungunya FeverHantavirus Pulmonary Syndrome

Condition Hierarchy (Ancestors)

Euglenozoa InfectionsProtozoan InfectionsParasitic DiseasesInfectionsSkin Diseases, ParasiticVector Borne DiseasesSkin Diseases, InfectiousSkin DiseasesSkin and Connective Tissue DiseasesSpirochaetales InfectionsGram-Negative Bacterial InfectionsBacterial InfectionsBacterial Infections and MycosesRickettsiaceae InfectionsTick-Borne DiseasesChlamydophila InfectionsChlamydiaceae InfectionsBorrelia InfectionsEncephalitis, ArbovirusEncephalitis, ViralCentral Nervous System Viral DiseasesCentral Nervous System InfectionsInfectious EncephalitisArbovirus InfectionsVirus DiseasesRNA Virus InfectionsFlavivirus InfectionsFlaviviridae InfectionsEncephalitisBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesNeuroinflammatory DiseasesHepatitis, Viral, HumanHepatitisLiver DiseasesDigestive System DiseasesMosquito-Borne DiseasesAlphavirus InfectionsTogaviridae InfectionsHantavirus InfectionsBunyaviridae InfectionsRespiratory InsufficiencyRespiration DisordersRespiratory Tract Diseases

Study Officials

  • CHARLOTTE BOULLE, MD

    University Hospital, Montpellier

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SCREENING
Intervention Model
SINGLE GROUP
Model Details: cross-sectional study with minimal risk and constraints
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 27, 2025

First Posted

March 5, 2025

Study Start

March 3, 2025

Primary Completion

October 3, 2025

Study Completion

October 3, 2025

Last Updated

March 5, 2025

Record last verified: 2025-02

Locations