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Cybersickness imAgiNg Olfactory Evocation

Cybersickness imAgiNg Olfactory Evocation

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05308433
Acronym
CANOE
Enrollment
30
Registered
2022-04-04
Start date
2022-04-13
Completion date
2022-10-26
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

fMRI

Brief summary

The aim of this study is to, using fMRI, compare brain activations during olfactory imagery induced by different visual supports (words, pictures, colors and colored arrangements) in healthy subjects. This will allow us to choose the best olfactory imagery facilitator and to assess its effect on cybersickness.

Interventions

DEVICEFunctional MRI

The volunteer will have to imagine the smells evoked by different visual aids. This task will be carried out during 2 acquisition runs of about 10 minutes each. The volunteer should note (on a scale from 1 to 4) the pleasantness of the smell evoked.

OTHERVirtual Reality: control

The volunteer will be immersed in a virtual maritime environment with nauseating characteristics. In the center of the maritime scene, it will be visible the black outlines of a frame. Every minute, the volunteer will be asked to verbalize the level of his general condition via the Fast Motion Sickness Scale (1 to 20).

OTHERVirtual Reality: experimental

The volunteer will be immersed in a virtual maritime environment with nauseating characteristics. The visual support inserted in the center of the virtual scene will be the one defined as being the most facilitator of the olfactory imagination during the fMRI examination. The volunteer will be asked to concentrate on the smell evoked by this support. Every minute, the volunteer will be asked to verbalize the level of his general condition via the Fast Motion Sickness Scale (1 to 20).

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* to be of French nationality who has always lived in metropolitan France; * to be right-handed person; * to be enrolled in a social security plan; * to be able to understand the instructions given; * to have underwent a pre-inclusion medical examination; * to give a written consent; * Person with a strong capacity for olfactory imagination: having obtained a score strictly below 2.5 on the fVOIQ olfactory imagination questionnaire.

Exclusion criteria

* to have an inability to read French; * to be recognized as a synesthete; * to have a professional activity requires intense olfactory activity; * to have a partial or total loss of smell (hyposmia, anosmia); * to have qualitative smell disorders (carcosomia, hyperosmia, phantosmia, parosmia); * to have smell disorders of neurological, post-traumatic or neurodegenerative origin; * to have uncorrected or poorly corrected visual disturbances; * to have vestibular disorder diagnosed; * any contraindication to MR examination (active medical device, ferromagnetic foreign body, pregnancy, morbid obesity, claustrophobia, … ); * subject under a measure of legal protection.

Design outcomes

Primary

MeasureTime frameDescription
Comparison of cerebral activations between the different supports mediating the olfactory imagination during the execution of the fMRI tasks.Baseline (J0)The cerebral activations between the different supports mediating the olfactory imagination will be compared in terms of localization and intensity of the variations of the BOLD signal during the execution of the fMRI tasks.

Secondary

MeasureTime frameDescription
Determination of the visual support allowing the strongest olfactory imagination during the fMRI by subjective evaluations using two 4-level Likert scales.Baseline (J0)Subjective evaluations will be carried out using two 4-level Likert scales.
Determination of the visual support allowing the strongest olfactory imagination during the fMRI test by the cerebral activations in areas recognized for their implications in the olfactory imagination.Baseline (J0)The cerebral activations will be measured by the intensity of the variations of the BOLD signal during the execution of the fMRI tasks.
Description of the evolution of the cardiac activity during olfactory imagination tasks in fMRI.Baseline (J0)The cardiac activity will be evaluated by the R-wave interval. The cardiac activity will be recorded via the ECG during olfactory imagination tasks in fMRI.
Description of the evolution of the respiratory activity during olfactory imagination tasks in fMRI.Baseline (J0)The respiratory activity will be evaluated by the respiratory rate. The respiratory activity will be recorded via the respiratory belt during olfactory imagination tasks in fMRI.
Evaluation of the state of discomfort in virtual reality by measuring the cardiac activity.Baseline (J0) and 6 months maximum after J0 (V1)Cardiac activity will be evaluated by the R-wave interval. Cardiac activity during immersion will be recorded by the cardio-respiratory belt.
Evaluation of the state of discomfort in virtual reality by the "Simulator Sickness Questionnaire" (SSQ) before and after immersion.Baseline (J0) and 6 months maximum after J0 (V1)The participant will answer to the "Simulator Sickness Questionnaire" (SSQ) before and after immersion (minimum=0 and maximum=235,62). A higher score means a more severe discomfort.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 16, 2026