Monitoring Antioxidant/Redox Status at Concordia (MARS-C)

Active, not recruiting

• Conditions: Oxidative Stress

• Registration Number: NCT04197193
• Lead Sponsor: University of Southampton

Brief Summary

The European Space Agency (ESA) runs a research centre in Antarctica as an earth-based model for long duration deep-space missions. Just like astronauts travelling into space, crew-members overwintering at this Concordia base are exposed to a number of extreme environmental stressors; including high altitude (approximately 3800m); extreme cold; long periods of 24 hour darkness or daylight; and complete isolation. The investigators will recruit up to 30 over-wintering crew members working at this station for ESA over a 2 year period and observe how their bodies adapt and respond to the stress of living and working in this environment. The investigators will collect blood, saliva and urine samples, together with ultrasound images of muscle mass and grip strength measurements at regular intervals throughout their deployment to Antarctica. These samples will be transported back to Southampton to be analysed for biochemical levels of stress. During the final month of their stay, all participants will be randomised to receive a daily nutritional drink which is either high or low in targeted dietary supplements. Following similar studies that the investigators has successfully performed over shorter durations at high altitudes previously, they hypothesise that levels of stress experienced in extreme environments such as Antarctica or deep space can be reduced with targeted nutritional supplementation. These findings may become important to members of the general public as commercial aviation moves increasingly towards using low space-orbital vehicles to drastically reduce international travel times over the coming decade.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-12-04
• Study First Submitted QC: 2019-12-11
• Study First Posted: 2019-12-13
• Study Start: 2022-10-03
• Status Verified: 2024-01
• Last Update Submitted: 2024-01-09
• Last Update Posted: 2024-01-11
• Primary Completion: 2024-12
• Study Completion: 2024-12

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Adult
• Member of Concordia station over-wintering crew
• Able to give written informed consent
• Fluent in either English, French or Italian

Exclusion Criteria

• Participating in another interventional research study during the deployment to Concordia

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hand grip strength	up to 10 months	Forearm muscle / grip strength recorded non-invasively using a hand grip dynamometer

Secondary Outcome Measures

Name	Time	Method
Oxidative stress	up to 10 months	Nitrate, nitrite, nitroso species, FRAP, TFTs, glutathione ratios, 8-isoprostane,
Muscle mass	up to 10 months	cross sectional forearm muscle area recorded a standardised way using medical ultrasound
Lake Louise Score 2018	up to 10 months	A validated measure of altitude related symptoms and illness which scores symptoms across 4 different domains: headache, GI disturbance, fatigue \& dizziness. Each is scored from 0 - 3 (for no symptoms to very debilitating respectively) and a total score of 3 or more including at headache symptoms is required for a positive diagnosis of Acute Mountain Sickness

Trial Locations

Locations (1)

University of Southampton; 🇬🇧 Southampton, United Kingdom