Evidence map›Paper›PMID 40186622›Full record

ArticleExperimental brain research2025

Construction of a computational model of individual progression of motion sickness symptoms based on subjective vertical conflict theory.

Shota Inoue, Van Trong Dang, Hailong Liu, Takahiro Wada

Abstract read
In one paragraph

Article in Experimental brain research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Shota InoueDivision of Information Science, Nara Institute of Science and Technology, 8916-5, Takayama-cho, Ikoma, Nara, 630-0192, Japan.
Van Trong DangDivision of Information Science, Nara Institute of Science and Technology, 8916-5, Takayama-cho, Ikoma, Nara, 630-0192, Japan.
Hailong LiuDivision of Information Science, Nara Institute of Science and Technology, 8916-5, Takayama-cho, Ikoma, Nara, 630-0192, Japan.
Takahiro WadaDivision of Information Science, Nara Institute of Science and Technology, 8916-5, Takayama-cho, Ikoma, Nara, 630-0192, Japan. t.wada@is.naist.jp.ORCID http://orcid.org/0000-0002-4518-8903

Funding

Japan Society for the Promotion of Science 21K18308Japan Society for the Promotion of Science 24H00298
6 · The paper itself

Abstract

Computational models predicting motion sickness have advanced, particularly those based on subjective vertical conflict (SVC) theory. While SVC-based models primarily predict motion sickness incidence (MSI), which is defined as the percentage of people who would vomit under a given motion, models predicting milder individual symptoms, which are crucial for daily applications, are still required. Recently, computational models predicting vestibular motion-sickness progression using the SVC theory have been developed by changing the output of a 6DOF-SVC model from MSI to the Misery Scale (MISC), a subjective measure of symptom progression. In practical applications, the ability to predict MISC for unseen motions is crucial. The present study conceived a method for predicting MISC beyond a certain point in the future by identifying parameters from data collected up to that point. Therefore, this study investigates the effect of the number of data points used for parameter identification on the future prediction accuracy. Observed MISC responses from participants exposed to linear lateral motion in darkness were used for model validation. The results indicated that prediction accuracy increased as more data points were included. On average, using more than 5-10 min of data significantly increased the accuracy compared to a model using averaged parameter sets across participants, although the tendency significantly differed based on an individual's MISC history. A trial considering individual MISC histories, in which data points were defined when the observed MISC first reached certain levels, showed a general trend of improved accuracy when data up to MISC Level 3 was used. The findings of this study demonstrate that motion sickness symptom progression can be predicted with reduced error by incorporating individual symptom histories, thereby providing a foundation for the development of personalized motion sickness prediction models applicable to broader applications.

Indexed as

Computer SimulationMotion PerceptionMotion SicknessAdultDisease ProgressionFemaleHumansMaleYoung AdultComputational modelIndividual symptom progression predictionMotion sicknessSubjective vertical conflict theory

Identifiers

PMID40186622
PMCPMC11972198

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.