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NCT04859868 · ClinicalTrials.gov registry record · NA

Non-pharmaceutical Motion Sickness Mitigation

A NA study, sponsored by Mayo Clinic.

Completed
Registry status
NA
Development phase
29
Enrollment target

NCT04859868: Completed NA study, sponsored by Mayo Clinic.

NCT04859868 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 29 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT04859868, a NA study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
NA
Development phase
29 participants
Enrollment target

Study Summary

The purpose of this study is evaluate the effect of timing and magnitude on the administration of our nonpharmaceutical treatment to motion sickness, and to evaluate the effect of Galvanic Vestibular Stimulation (GVR) amplitude on functional fitness task performance.

Primary Outcome

Motion Perception verbal report using a visual analog scale (1-100) will be recorded during the rotation of the chair (1=feeling no motion perception; 100=feeling the maximum motion perception)

Interventions

  • DEVICE Galvanic Vestibular Stimulation

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2021-03-12
Est. Completion 2022-08-30
Phase NA
Mayo Clinic

2,844 total trials

What the finished NCT04859868 record still lists

NCT04859868 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Galvanic Vestibular Stimulation is the first listed.

NCT04859868 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04859868 about?

NCT04859868 is a clinical study titled "Non-pharmaceutical Motion Sickness Mitigation". The purpose of this study is evaluate the effect of timing and magnitude on the administration of our nonpharmaceutical treatment to motion sickness, and to evaluate the effect of Galvanic Vestibular Stimulation (GVR) amplitude on functional fitness task performance.

What is the current status of trial NCT04859868?

This trial is currently completed. It is a NA study. The enrollment target is 29 participants. The study started on 2021-03-12. Estimated completion is 2022-08-30.

What interventions are being tested in trial NCT04859868?

The interventions under investigation include: Galvanic Vestibular Stimulation (DEVICE).

Who is sponsoring clinical trial NCT04859868?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04859868's enrollment target sits among peer trials

29 1702nd of 2000 higher than 297 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04859868, the US trial registry maintained by the National Library of Medicine. NCT04859868 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.