ClinicalTrials.gg
Not yet recruitingNCT07619469Updated Jun 26, 2026

Motion Sickness Severity and Sensorimotor Performance

An observational study in Motion Sickness, Somatosensory Disorders and Dizziness, sponsored by Istinye University. Not yet recruiting. Open to participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-06-26.

Sponsored by Istinye University · Observational

From the registry’s dates

  • Primary completion was expected by Aug 2026, 3 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
41
Ages
18 Years to 40 Years
Sex
All
01

Study 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).

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Conditions studied

  • Motion Sickness
  • Somatosensory Disorders
  • Dizziness
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In context

Motion Sickness

50 studies on the registry are indexed under Motion Sickness; 9 are open to participants now.

Browse Motion Sickness studies →

Lead sponsor

Istinye University is the lead sponsor of 221 studies on the registry; 94 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of adult individuals aged between 18 and 40 years who exhibit susceptibility to motion sickness.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
41 participants (estimated)
Patient registry
No

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."

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What researchers measure

Primary outcomes

  1. Motion Sickness Severity (Graybiel Score)

    Used 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).

    Time frame: 1 hour

  2. Static Balance

    Evaluated objectively using the ProKin® computerized balance system. Participants stand on the platform under conditions: double-leg with eyes open.

    Time frame: 1 hour

  3. Dynamic Balance Performance

    Evaluated using the ProKin® system.

    Time frame: 1 hour

Secondary outcomes

  1. Knee Joint Proprioception

    Evaluated in supine and prone positions, targeting knee angles of 15°, 30°, 60°, and 90° using the Clinometer digital inclinometer smartphone application.

    Time frame: 1 hour

  2. Nine-Hole Peg Test (9HPT) Completion Time

    Used 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.

    Time frame: 1 hour

  3. Tandem Walk Test Error Count

    Participants 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.

    Time frame: 1 hour

  4. Visual Reaction Time

    Evaluated using the mobile application-based BlazePod.

    Time frame: 1 hour

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Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jun 2026; primary completion for Aug 2026, 2 months later.

How these figures are worked out, and which studies are left out of them.

Registered
May 26, 2026
First posted
Jun 2, 2026
StartEst.
Jun 1, 2026
Primary completionEst.
Aug 2, 2026
CompletionEst.
Aug 5, 2026
Last update
Jun 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07619469
Lead sponsor
Istinye University
Responsible party
Yunus Emre Tutuneken (Dr. Assistant Professor, Istinye University) — Principal investigator
First posted
Jun 2, 2026
Start date
Jun 1, 2026 (estimated)
Primary completion
Aug 2, 2026 (estimated)
Completion
Aug 5, 2026 (estimated)
Last update
Jun 26, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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