Massper: Influence of Gravity on the Size-mass Illusion

Sponsor
University Hospital, Caen (Other)
Overall Status
Unknown status
CT.gov ID
NCT02507453
Collaborator
(none)
36
1
1

Study Details

Study Description

Brief Summary

Parabolic flight is the only ground-based condition in which free-fall (0G) can be created long enough for safely testing changes in human perception and behavior. In addition to the 0G period, parabolic flight generates equal duration periods of 1.8G, which present another unique opportunity to test the same responses to hypergravity and back to 1G.

It is well known that performance decrements occur in astronauts during and after gravity level transitions. Illusions are commonly felt in orbit as well disorientation and perceptual limitations, mainly due to both psycho-physiological changes and adaptation and lack of familiar points of reference in the space environment. Studies performed during previous space missions showed several changes occurring in different gravity conditions, pointing out, for example, that colors and shadows were misleading, the depth and distance perception were weakened, and the linear perspective was lost. Visual perception is of primary importance for spatial orientation and object recognition because the static vestibular (otolithic) and proprioceptive signals are absent when free-floating. Consequently, astronauts become increasingly dependent on vision to perceive motion and orientation. All these factors play an important role in the adaptation of humans to spaceflight that needs to be analyzed to understand the underlying mechanisms that regulate human psycho-physiological adaptive process to changing gravity. Human psycho-physiological health has to be safeguarded and possibly improved when long-term human space missions are programmed in the near future.

The primary objective of this experiment is to investigate if the SWI illusion is present in altered gravity environments. Since weight cannot be estimated in 0G, investigators have developed a procedure during which the subject is asked to estimate the objects' mass by shaking them rather than lifting them. Our results in 1G indicate that a size-mass illusion (SMI) is also present in 1G. Our hypothesis is that the previously observed alteration in 3D visual perception in 0G, particularly in the height of 3D objects, as well as the change in proprioceptive inputs, will be responsible for changes in the SMI in 0G and 1.8G compared to 1G. In a separate proposal, investigators will also propose to perform this experiment using the ESA short-arm human centrifuge (SAHC), with subjects exposed to various centrifugal force levels, to further investigate the role of proprioceptive cues in the size-mass illusion.

Condition or Disease Intervention/Treatment Phase
  • Other: parabolic flight
  • Other: mass/weight perception estimation
  • Device: ESA short-arm human centrifuge (SAHC)
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Study Start Date :
Oct 1, 2013
Anticipated Primary Completion Date :
Oct 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Other: Influence of Gravity on the Size-mass Illusion

to investigate the interaction between perceived size and perceived mass of objects in 0G and 1.8G compared to 1G using the size-mass illusion (SMI)

Other: parabolic flight

Other: mass/weight perception estimation
estimate the mass/weight perception, expressed by verbally report the absolute and relative mass of the object using a scale from 1 to 10 (1 being light and 10 being heavy)

Device: ESA short-arm human centrifuge (SAHC)

Outcome Measures

Primary Outcome Measures

  1. perceived size and perceived mass of objects in 0G and 1.8G compared to 1G using the size-mass illusion (SMI) (composite) [baseline]

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy volunteers (men or women)

  • Aged from 21 to 65

  • Right handed

  • 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 have given their written stated consent

  • Who has passed a medical examination similar to a standard aviation medical examination for private pilot aptitude (JAR FCL3 Class 2 medical examination). There will be no additional test performed for subject selection.

Exclusion Criteria:
  • Person who took part in a previous biomedical research protocol, of which exclusion period is not terminated

  • Pregnant women

Contacts and Locations

Locations

Site City State Country Postal Code
1 Umr Ucbn/Inserm U1075 Comete Caen CEDEX Basse-Normandie France 14032

Sponsors and Collaborators

  • University Hospital, Caen

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Caen
ClinicalTrials.gov Identifier:
NCT02507453
Other Study ID Numbers:
  • 13-028
First Posted:
Jul 24, 2015
Last Update Posted:
Jul 24, 2015
Last Verified:
Jul 1, 2015
Keywords provided by University Hospital, Caen

Study Results

No Results Posted as of Jul 24, 2015