NCT07278245

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

87
On Track

Trial Health Score

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

Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

October 27, 2025

Completed
29 days until next milestone

First Submitted

Initial submission to the registry

November 25, 2025

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 27, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

December 12, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 27, 2026

Completed
Last Updated

February 5, 2026

Status Verified

February 1, 2026

Enrollment Period

1 month

First QC Date

November 25, 2025

Last Update Submit

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 INTERVENTION

Untrained group

Trained

EXPERIMENTAL

Trained with the exoskeleton

Other: Training with an exoskeleton

Interventions

Training to perform an aiming task under simulated hypergravity via an exoskeleton

Trained

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

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

Locations