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NCT05622344 · ClinicalTrials.gov registry record · NA

StableEyes With Active Neurofeedback

A NA study of Vestibular Schwannoma and Vestibular Disorder, sponsored by Johns Hopkins University.

Recruiting
Registry status
NA
Development phase
48
Enrollment target
2
Study locations

NCT05622344: Recruiting NA study of Vestibular Schwannoma and Vestibular Disorder, sponsored by Johns Hopkins University.

NCT05622344 is a NA study of Vestibular Schwannoma and Vestibular Disorder that is actively recruiting participants, run by Johns Hopkins University. The registered enrollment target is 48 participants, roughly in line with the 46-participant average among 7 other Vestibular Schwannoma trials with a reported enrollment target. The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05622344, a NA study of Vestibular Schwannoma and Vestibular Disorder, is actively recruiting participants, sponsored by Johns Hopkins University.

RECRUITING
Registry status
NA
Development phase
48 participants
Enrollment target
2
Study locations

Study Summary

The investigators have developed a self-administered rehabilitation tool that incrementally guides the user to increase head motion to mitigate motion sickness and enhance postural recovery following centrifugation or unilateral vestibular nerve deafferentation surgery.

Primary Outcome

Subjective rating of motion sickness intensity from 0 to 10. Zero denotes absent motion sickness while 10 denote vomiting.

Interventions

  • BEHAVIORAL Traditional Therapy
  • DEVICE SWAN

Study Locations (2)

Maryland

  • Johns Hopkins University - Baltimore

Ohio

  • Naval Medical Research Unit - Dayton

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2022-08-08
Est. Completion 2026-09-30
Phase NA
Johns Hopkins University

1,448 total trials

What NCT05622344 shows while recruiting

NCT05622344 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, roughly in line with the 46-participant average among 7 other Vestibular Schwannoma trials with a reported enrollment target.

The record links to 4 conditions, with Vestibular Schwannoma appearing as the primary indexed condition, and to 2 interventions - of which Traditional Therapy is the first listed.

NCT05622344 reports a single indexed study location in Maryland, Ohio.

Frequently Asked Questions

What is clinical trial NCT05622344 about?

NCT05622344 is a clinical study titled "StableEyes With Active Neurofeedback". The investigators have developed a self-administered rehabilitation tool that incrementally guides the user to increase head motion to mitigate motion sickness and enhance postural recovery following centrifugation or unilateral vestibular nerve deafferentation surgery.

What is the current status of trial NCT05622344?

This trial is currently recruiting. It is a NA study. The enrollment target is 48 participants. The study started on 2022-08-08. Estimated completion is 2026-09-30.

What conditions does trial NCT05622344 study?

This clinical trial studies the following conditions: Vestibular Schwannoma, Vestibular Disorder, Motion Sickness, Space Motion Sickness.

What interventions are being tested in trial NCT05622344?

The interventions under investigation include: Traditional Therapy (BEHAVIORAL), SWAN (DEVICE).

Who is sponsoring clinical trial NCT05622344?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05622344 being conducted?

This trial has 2 study locations across Maryland, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT05622344, the US trial registry maintained by the National Library of Medicine. NCT05622344 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.