Rendering of a Local 1g Environment for Enhanced Motor Learning in Altered Gravity

Healthy Clinical Trial

— Sim1g  

Official title:

Rendering of a Local 1g Environment for Enhanced Motor Learning in Altered Gravity

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03978910
• Other study ID #: 18-210
• Status: Recruiting
• Phase: N/A
• Start date: April 1, 2019
• Est. completion date: May 30, 2021

Study information

• Verified date: June 2019
• Source: University Hospital, Caen
• Contact: Stephane Besnard
• Phone: +33 231.06.81.64
• Email: stephane.besnard[@]unicaen.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Human motor adaptation is crucial to adapt to new environments, such as altered gravity. Dexterous manipulation and fine movements in space require learning new coordinated motor actions. Traditionally, adaptation mechanisms have been tested in laboratories with robotic devices that perturb specific task parameters unbeknownst to the participant. Over repetition, participants build a more accurate representation of the task dynamics and, eventually, improve performance. These perturbations are applied locally on the hand or limb while the dynamics of the rest of the body remains unaltered. These approaches are therefore limitative since they do not reflect ecological adaptation to globally changed dynamics, such as new gravitational environments. Parabolic flights, centrifuges and water immersion allow circumventing these limitations. Previous investigations in these contexts have highlighted the role of the global context in motor adaptation. However, it is unknown if global learning could benefit from exploiting known local dynamics. Here, we design an original task that will capture both the learning of arm movement kinematics as well as grasping forces for object manipulation in an ecologically valid design. We test whether executing this task in hypogravity with rendering of Earth gravity locally at the hand is beneficial or detrimental to task performance. By adopting the "negative picture" of conventional robotic approaches, these results will further our understanding of basic motor adaptation and provide insightful information on the optimal design and control of human-machine interfaces and wearable robots in space environments and other immersive dynamics.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 18
• Est. completion date: May 30, 2021
• Est. primary completion date: May 30, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Healthy volunteers (men or women).

• Aged from 18 to 65.

• Affiliated to a Social Security system and, for non-French resident, holding a European Health Insurance Card (EHIC).

• Who accepted to take part in the study.

• Who can take scopolamine or nautamine (medication against airsickness).

• Who have given their informed written stated consent.

• Who have passed a medical examination similar to a standard aviation medical examination for private pilot aptitude (JAR FCL3 Class 2 medical examination) and have been declared fit to fly. The examination must be less than one year before the experiment flight. There will be no additional test performed for participant selection.

Exclusion Criteria:

• Persons who took part in a previous biomedical research protocol, of which exclusion period is not terminated.

• Persons with any history of cerebral, cardiovascular or vestibular diseases.

• Persons with history of psychiatric diseases, including anxiety disorder.

• Persons whose medical condition has changed since the class 2-like medical examination.

• Pregnant women (urine pregnancy test for women of childbearing potential).

Related Conditions & MeSH terms

• Healthy

Intervention

Other:
• measurements of the accuracy of the reaching movements
Euclidian distance between final position and target

Locations

Country	Name	City	State
France	Caen Univerity Hospital	Caen

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	accuracy of the reaching movements	Euclidian distance between final position and target	baseline