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Not yet recruitingNCT07898930FARMHANDUpdated Nov 6, 2026

Farm-originated Antimicrobial Resistance Modeling: Exploring Humans-to-Animal Dissemination

An interventional study of Sample collection in Methicillin-Resistant Staphylococcus Aureus Colonization, sponsored by Centre Hospitalier de Saint-Brieuc. Not yet recruiting at 2 sites in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by Centre Hospitalier de Saint-Brieuc · Not applicable, Interventional, and Basic science

Updated Oct 27, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Antimicrobial resistance is a major public health issue. Methicillin resistance in Staphylococcus aureus (MRSA) is one of the indicators that is monitored particularly closely. In animals, pig farms, among others, have been identified as reservoirs of MRSA, with a risk of transmission to humans, particularly to individuals in direct contact with livestock. In France, the prevalence of MRSA in pig farms has increased markedly in recent years.

While cross-species transmission between pigs and humans in professional settings is well-documented, the temporal dynamics, the actual incidence of acquisition, and the associated determinants remain insufficiently characterized in France.

Adopting a "One Health" approach, this project aims to gain a better understanding of the mechanisms by which MRSA spreads between animal and human subpopulations and to incorporate these insights into a mathematical modeling framework.

Read the detailed description

The participants in this project will be farmers representing 20 different pig farms, the majority of which will be located in Brittany-a region recognized as the leading pork-producing area in France.

Participants will be asked to provide two types of samples, only one of which will contain personally identifiable data.

  • Nasal swabs: Participants in the study will be asked to perform a self-administered nasal swab once a month, at approximately the same time each month. This method was selected because it has demonstrated an acceptable level of participant compliance, as well as satisfactory validity for detecting S. aureus carriage in humans.
  • Dust samples: Participants will be asked to collect dust samples from the production floor-specifically in the room within the finishing facility that houses the oldest animals-by wiping surfaces with a small cloth. This method was chosen because dust in livestock-rearing environments has been identified as a reliable indicator of MRSA carriage status in pigs.

These successive samplings will be carried out over time in order to analyze carriage dynamics and estimate epidemiological parameters of interest. A modeling component will be incorporated to make use of the data collected.

02

Conditions studied

  • Methicillin-Resistant Staphylococcus Aureus Colonization

Keywords

  • Staphylococcus aureus
  • One health
  • Antibiotic resistance
03

In context

Staphylococcal Infections

303 studies on the registry are indexed under Staphylococcal Infections; 34 are open to participants now.

This study's planned enrollment of 20 is below the median of 124 across 198 interventional studies indexed under Staphylococcal Infections.

Browse Staphylococcal Infections studies →

Lead sponsor

Centre Hospitalier de Saint-Brieuc is the lead sponsor of 9 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 18 years of age or older,
  • Work full-time as a pig farmer on the participating farm,
  • Have regular contact with the animals, defined as at least 4 days per week,
  • Be willing to participate in the study and sign an form,
  • Agree to perform monthly self-administered nasal swab sampling and to provide data via a questionnaire.

Exclusion criteria

Exclusion Criteria:

  • Refusal to participate or inability to provide ,
  • Inability to perform monthly self-administered nasal swabs in accordance with the protocol,
  • Employment on a part-time basis, or status as an intern or apprentice within the operation,
  • No inclusion of persons targeted by Articles L. 1121-5 to L. 1121-8 and L. 1122-1-2 of the Public Health Code (e.g., minors, legally protected adults, etc.)
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Farmers representing 20 different pig farms

    Other: Sample collection

Interventions

  • OtherSample collection

    Participants will be asked to provide two types of samples, only one of which will contain personally identifiable information. * Nasal samples: a monthly self-collected nasal swab, performed at approximately the same time each month. * Dust samples: following the collection and storage of the nasal swab, participants will be asked to collect dust samples from the production area-specifically, from the room within the fattening facility that houses the oldest animals-by wiping surfaces using a small cloth.

06

What researchers measure

Primary outcomes

  1. To estimate the prevalence of nasal carriage of MRSA among pig farmers during the study period.

    The primary outcome measure is the prevalence of nasal carriage of MRSA among pig farmers during the study period, as determined by microbiological detection from self-collected nasal swabs.

    Time frame: From enrollment to the end of the study : 24 months

Secondary outcomes

  1. Describe the temporal dynamics of nasal carriage of Staphylococcus aureus among pig farmers and within farms.

    The prevalence of nasal carriage of MSSA among pig farmers.

    Time frame: From enrollment to the end of the study : 24 months

  2. Estimate the incidence of acquisition and clearance of MRSA and MSSA among pig farmers and within farms, based on repeated longitudinal measurements.

    The incidence of acquisition and clearance of MRSA and MSSA among pig farmers, estimated from repeated longitudinal measurements of nasal carriage.

    Time frame: From enrollment to the end of the study : 24 months

  3. Identify factors associated with the carriage and acquisition of MRSA among pig farmers.

    The prevalence and incidence of MSSA and MRSA within the pig farm environment.

    Time frame: From enrollment to the end of the study : 24 months

07

Study locations

2 sites
  • Anses Ploufragan - Plouzané - Niort, site de Ploufragan
    Ploufragan, 22440, France
    • Claire CHAUVIN, Dr · Contact
  • Centre Hospitalier de Saint-Brieuc - Paimpol - Tréguier, site de Saint-Brieuc
    Saint-Brieuc, 22000, France
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Nov 2026; primary completion for Nov 2028, 24 months later.

Of 30 non-industry interventional studies with no phase under Staphylococcal Infections, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 14 and three quarters within 57. This study's planned 24 months is above that.

Counting every sponsor, half of 32 studies reached it within 21 months; a quarter within 14 and three quarters within 57.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 21, 2026
First posted
Oct 27, 2026
StartEst.
Nov 2026
Primary completionEst.
Nov 2028
CompletionEst.
Nov 2028
Last update
Nov 6, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 27, 2026
Show all 2 updates
  1. Nov 6, 2026
    Minor edits only
    + 2 other changes: verification date and conditions
  2. Oct 27, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07898930
Lead sponsor
Centre Hospitalier de Saint-Brieuc
Collaborators
ANSES (Agence Nationale de Sécurité Sanitaire de l'alimentation, de l'environnement et du travail), National conservatory of arts and crafts (CNAM), Institut Pasteur
Responsible party
Sponsor
First posted
Oct 27, 2026
Start date
Nov 2026 (estimated)
Primary completion
Nov 2028 (estimated)
Completion
Nov 2028 (estimated)
Last update
Nov 6, 2026

Study contacts

Fanny BEGUIER
Contact
recherche.clinique@armorsante.bzh
0296018165 ext. +33
Marie-Pierre DUBAN
Contact
recherche.clinique@armorsante.bzh

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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