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CHOICE KERGUELEN 1: Consequences of Longterm Confinement on Immunity in the Sub-Antarctic Islands: Inclusion of Volunteers Before Departure to the Kerguelen Islands

CHOICE KERGUELEN 1: Consequences of Longterm Confinement on Immunity in the Sub-Antarctic Islands: Inclusion of Volunteers Before Departure to the Kerguelen Islands

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07065253
Enrollment
0
Registered
2025-07-15
Start date
2025-09-25
Completion date
2025-09-25
Last updated
2026-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Human Health in Extreme Conditions

Brief summary

Living for long periods in extreme environments-like Antarctic research stations or space missions-can have a significant impact on human health, especially on the immune system. Scientists have observed that people in such isolated conditions often experience more infections and a reactivation of viruses that usually stay dormant in the body, such as Herpes viruses. These changes affect both parts of the immune system: the rapid-response "innate" system and the slower, more specific "adaptive" system. These immune disruptions may be caused by multiple stressors: ongoing psychological stress, disturbed sleep and light cycles (circadian rhythm disruption), and the challenges of living in confined, isolated, and extreme environments. While space missions and Antarctic overwintering programs have provided some insight into these issues, scientists still lack a detailed understanding of how the immune system adapts-or fails to adapt-over time in such conditions. To help fill this gap, the CHOICE Kerguelen 1 study will recrut a group of healthy young adults who will spend one year (from November 2025 to November 2026) in Port-aux-Français, a remote French research station on the Kerguelen Islands in the sub-Antarctic. These volunteers are participating in a civic service program and will be living in a highly isolated environment for the duration of their mission. The CHOICE Kerguelen 1 study is conducted in collaboration with the French Polar Institute (IPEV).The goal of the study is to collect and store a broad range of biological samples-including blood, saliva, stool, urine, and hair-from these volunteers before they leave for the island, to have baseline medical state and baseline biological samples. These samples will integrate in to healthy volunteer biobank of CHU Angers, a type of biological archive that provided control samples for CHOICE Kerguelen 2 - a clinical study relating to follow-up of volunteers during civic service on the Kerguelen Islands

Interventions

blood ponction

urines collection

hair collection

OTHERsaliva collection

saliva collection

stools collection

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV
Institut Polaire Français Paul-Emile Victor (IPEV)
CollaboratorUNKNOWN

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

: * healthy people aged \> 18 years * Participant affiliated with or benefiting from a social security system * Participant has signed informed consent * Participant staying as an overwintering member at Kerguelen from November 2025 to November 2026

Exclusion criteria

* age \< 18 years * Pregnant, breastfeeding, or postpartum woman * immunocompromised people (primary immunodeficiency, HIV infection or immunosupressive treatment) * Person refusing to participate in the study * Person with a history of autoimmune disease - -Person deprived of liberty by judicial or administrative decision * Person undergoing involuntary psychiatric treatment * Person subject to a legal protection measure

Design outcomes

Primary

MeasureTime frameDescription
Blood samplesAt inclusion (before overwintering)Blood samples
Saliva samplesAt inclusion (before overwintering)Saliva samples
Urine samples.At inclusion (before overwintering)morning urine samples.
Hair samplesAt inclusion (before overwintering)Hair samples
Stool samplesAt inclusion (before overwintering)Stool samples

Countries

France

Contacts

PRINCIPAL_INVESTIGATORCharline MIOT

University Hospital, Angers

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026