Effects of Active Upper-Limb Exoskeleton Training in Simulated Hyper-Gravity on Fine Motor Performance, Brain-Muscle Connectivity, Cardiovascular System and Stress Responses in Real Hyper-Gravity
EGOS
2 other identifiers
interventional
12
1 country
1
Brief Summary
The aim of the study presented here is to assess the effects of exoskeleton training on performance in a real hypergravity situation. In particular, it will analyze fine motor control, autonomic nervous system regulation and metabolic responses. To this end, the study will compare two groups during a pointing exercise in a centrifuge (hypergravity). One group will have been trained to do this exercise using an exoskeleton, while the other will have been familiarized with the task without the exoskeleton. It will assess whether the exoskeleton can be an effective and accessible training tool for astronauts.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 27, 2025
CompletedFirst Submitted
Initial submission to the registry
November 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 27, 2025
CompletedFirst Posted
Study publicly available on registry
December 12, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 27, 2026
CompletedFebruary 5, 2026
February 1, 2026
1 month
November 25, 2025
February 4, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Task performance (movement accuracy)
Task performance (movement accuracy) is defined as the difference between the position touched on the screen and the position of the displayed target. The participants will be required to perform an aiming movement task using their right arm, directed toward a target.The participants will need to point to the center of the displayed target.
From familiarisation sessions (Day 1 to Day 4) to testing day at Day 5.
Study Arms (2)
Control
NO INTERVENTIONUntrained group
Trained
EXPERIMENTALTrained with the exoskeleton
Interventions
Training to perform an aiming task under simulated hypergravity via an exoskeleton
Eligibility Criteria
You may qualify if:
- Maximum weight of 90 kg
- Maximum sitting butt-to-shoulder distance of 70 cm
- Certified as healthy by a comprehensive clinical assessment
- Normal or corrected to normal vision
- Right-handed tested with Edinburgh-Handedness-Inventory-Test (≥6th percentile, on https://www.brainmapping.org/shared/Edinburgh.php)
- Non smokers
- No alcohol or drug dependence, no medical treatment on a regular basis
- Affiliated to a Social Security system and, for non-French resident, holding a European Health Insurance Card (EHIC) or a Global Health Insurance Card (GHIC).
- Free of any engagement during the study
- Test subjects must be able to understand and speak English
- Who agreed to take part in the study and signed the informed consent
You may not qualify if:
- Left-handed tested with Edinburgh-Handedness-Inventory-Test (\<6th percentile)
- Subjects with experience in experiments on a short arm human centrifuge or under real hyper-gravity
- Non-tolerance to the centrifugation
- Any history or presence of clinically relevant chronic disease
- Refusal to give permission to contact his general practitioner,
- Subject who, in the judgment of the investigator, is likely to be non-compliant during the study, or unable to cooperate because of a language problem or poor mental development,
- Subject who has received more than 6000 Euros within 12 months for being a research subject,
- Subject who cannot be contacted in case of emergency,
- Vulnerable people according to law "Code de la Santé Publique" (L1121-5 to L1121-8)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medes - Imps
Toulouse, Occitanie, 31400, France
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 25, 2025
First Posted
December 12, 2025
Study Start
October 27, 2025
Primary Completion
November 27, 2025
Study Completion
January 27, 2026
Last Updated
February 5, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share