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Motion Sickness Severity and Sensorimotor Performance

The Relationship of Balance, Proprioception, Coordination, and Reaction Time Measurements With Motion Sickness Severity in Individuals With Motion Sickness: A Cross-Sectional Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07619469
Enrollment
41
Registered
2026-06-02
Start date
2026-06-01
Completion date
2026-08-05
Last updated
2026-06-26

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

Conditions

Dizziness, Motion Sickness, Somatosensory Disorders

Brief summary

Background: Motion sickness (MS) is a common syndrome characterized by autonomic and behavioral symptoms, such as nausea and dizziness, resulting from exposure to motion stimuli. Its pathophysiology is closely linked to sensory conflict and postural instability theories. While previous studies suggest that postural control, proprioception, and reaction times are affected in individuals susceptible to MS, there is a lack of comprehensive, comparative research evaluating all these parameters concurrently within the same cohort using standardized methods. Objective: This study aims to systematically measure balance, proprioceptive sensitivity, coordination, and reaction time parameters, and quantitatively analyze their relationship with motion sickness severity. Methodology: In this prospective, cross-sectional study, at least 41 participants aged 18-40 with motion sickness will be recruited. Participants will undergo motion sickness susceptibility and severity grading using the Motion Sickness Susceptibility Questionnaire Short Form (MSSQ-SF) and the Graybiel Scale. Objective assessments will include static and dynamic balance testing (ProKin®), knee joint position sense (Clinometer app), manual dexterity and dynamic balance coordination (Nine-Hole Peg Test, Tandem Walk, Romberg Test), and upper/lower extremity reaction time measurements (BlazePod system).

Interventions

OTHERStandardized Sensorimotor Assessment and Motion Sickness Provocation Protocol

Participants will undergo a standardized battery of sensorimotor assessments, including static/dynamic balance tracking, knee joint position sense testing, manual dexterity/coordination tasks, and upper/lower extremity reaction time measurements, alongside a controlled motion sickness provocation session using a randomized chair-rotation protocol."

Sponsors

Istinye University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Individuals aged between 18 and 40 years. * Diagnosed with motion sickness according to the Motion Sickness -Susceptibility Questionnaire Short Form (MSSQ-SF). * Normal hearing acuity. * No history of acute or chronic vestibular disease, other than motion sickness. * Normal or corrected-to-normal vision. * Adequate physical capability to fully perform the measurement protocols, including balance, proprioception, coordination, and reaction time tests.

Exclusion criteria

* Presence of any physical or orthopedic problem that could interfere with testing. * History of acute or chronic instability, unsteadiness, or vertigo. * Severe visual impairment. * History of prior ear surgery. * Presence of any neurological condition or disorder. * History of migraines. * Current use of medications that could affect balance or vestibular function (e.g., vestibular suppressants, sedatives). * Use of alcohol or psychoactive substances within the last 48 hours prior to testing.

Design outcomes

Primary

MeasureTime frameDescription
Motion Sickness Severity (Graybiel Score)1 hourUsed to grade the clinical severity of acute motion sickness symptoms (including nausea, cold sweating, increased salivation, and dizziness) following a randomized chair-rotation provocation protocol. 0 (Minimum) to 50 points (Maximum). Higher scores indicate greater symptom severity, representing a worse clinical outcome (scores of 16 or above designate frank sickness).
Static Balance1 hourEvaluated objectively using the ProKin® computerized balance system. Participants stand on the platform under conditions: double-leg with eyes open.
Dynamic Balance Performance1 hourEvaluated using the ProKin® system.

Secondary

MeasureTime frameDescription
Knee Joint Proprioception1 hourEvaluated in supine and prone positions, targeting knee angles of 15°, 30°, 60°, and 90° using the Clinometer digital inclinometer smartphone application.
Nine-Hole Peg Test (9HPT) Completion Time1 hourUsed to assess upper extremity dexterity and fine motor coordination. Participants place nine pegs into the holes one by one and then remove them as quickly as possible.
Tandem Walk Test Error Count1 hourParticipants walk barefoot along a straight line for 10 steps, placing the heel of one foot directly against the toe of the other foot with arms relaxed at their sides.
Visual Reaction Time1 hourEvaluated using the mobile application-based BlazePod.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 27, 2026