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Procedure
SWAN Therapy for Vestibular Disorders (SWAN Trial)
N/A
Recruiting
Led By Matthew Stewart, MD PhD
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
In good general health as evidenced by medical history or diagnosed with unilateral vestibular schwannoma
Be older than 18 years old
Must not have
Current use of anti-nausea medication
Presence of cervical spine pathology that limits head motion to < 30 degrees in the horizontal or vertical plane (i.e. degenerative disc disease, rheumatoid arthritis)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up daily for up to 4 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a device that helps patients practice head movements to reduce motion sickness and improve balance after certain surgeries. It is aimed at patients who have undergone specific surgeries and experience motion sickness and balance problems. The device guides head movements and monitors for nausea to help patients gradually get used to motion.
Who is the study for?
This trial is for people in good health or with unilateral vestibular schwannoma, who can follow the SWAN/vestibular rehab regimen and commit to the study's duration. It excludes those on anti-nausea meds, recent motion sickness treatments, legally blind individuals, or those with neck/spine issues limiting head movement.
What is being tested?
The trial tests a self-help tool called SWAN against traditional therapy. It aims to reduce motion sickness and improve balance after certain surgeries by training users to gradually increase head movements.
What are the potential side effects?
While specific side effects are not listed, this type of physical rehabilitation may cause temporary discomfort, dizziness or nausea as participants adjust their head movements during exercises.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am generally healthy or have a unilateral vestibular schwannoma.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently taking medication for nausea.
Select...
I have a neck condition that limits my head movement.
Select...
I cannot walk or stand on my own due to a recent surgery or bone condition.
Select...
I haven't used any experimental drugs or methods for motion sickness in the last 30 days.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ daily for up to 4 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~daily for up to 4 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Motion sickness intensity as assessed by subjective rating
Secondary study objectives
Change in Daily Activity as assessed by an activity monitor
Change in Foam Stance - Eyes Closed
Change in Foam Stance - Eyes Closed with head motion
+12 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
4Treatment groups
Experimental Treatment
Active Control
Group I: SWAN VPT JHUExperimental Treatment1 Intervention
Subjects that have had their eighth cranial nerve resected will receive the automated vestibular rehabilitation method
Group II: SWAN Motion Sick DaytonExperimental Treatment1 Intervention
Healthy control subjects that meet similar similar physical characteristics of astronauts will receive the automated vestibular rehabilitation method post motion sickness.
Group III: Traditional VPT JHUActive Control1 Intervention
Subjects that have had their eighth cranial nerve resected will receive traditional vestibular rehabilitation exercises at Johns Hopkins University (JHU) site.
Group IV: Traditional Motion Sick DaytonActive Control1 Intervention
Typically, the suggestion for treating motion sickness once it has started is to avoid motion. Therefore, healthy control subjects that meet similar similar physical characteristics of astronauts will not receive any post motion sickness treatment.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for motion sickness include antihistamines, anticholinergics, and vestibular rehabilitation exercises. Antihistamines, such as dimenhydrinate, work by blocking histamine receptors in the brain, which helps reduce nausea and vomiting.
Anticholinergics, like scopolamine, inhibit the action of acetylcholine, a neurotransmitter involved in motion sickness, thereby reducing symptoms. Vestibular rehabilitation exercises, including the self-administered rehabilitation tool studied in the trial, aim to desensitize the vestibular system by gradually increasing head motion.
This incremental exposure helps the brain adapt to motion stimuli, reducing the severity of motion sickness. These treatments are crucial for patients as they target the underlying mechanisms of motion sickness, providing relief and improving their ability to engage in daily activities without discomfort.
Is vestibular rehabilitation effective in improving dizziness and function after unilateral peripheral vestibular hypofunction? An abridged version of a Cochrane Review.
Is vestibular rehabilitation effective in improving dizziness and function after unilateral peripheral vestibular hypofunction? An abridged version of a Cochrane Review.
Find a Location
Who is running the clinical trial?
Johns Hopkins UniversityLead Sponsor
2,323 Previous Clinical Trials
14,874,259 Total Patients Enrolled
National Aeronautics and Space Administration (NASA)FED
30 Previous Clinical Trials
1,830 Total Patients Enrolled
2 Trials studying Motion Sickness
110 Patients Enrolled for Motion Sickness
Matthew Stewart, MD PhDPrincipal InvestigatorJohns Hopkins University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am willing to follow a specific balance or dizziness treatment plan.I cannot walk or stand on my own due to a recent surgery or bone condition.I haven't used any experimental drugs or methods for motion sickness in the last 30 days.I am generally healthy or have a unilateral vestibular schwannoma.I am willing and able to follow the study rules and attend all appointments.I am currently taking medication for nausea.I am generally healthy or have a unilateral vestibular schwannoma.You are willing to comply with all study procedures and are available for the duration of the study.I am willing to follow a specific balance and dizziness exercise program.You have very poor vision, worse than 20/200.I have a neck condition that limits my head movement.
Research Study Groups:
This trial has the following groups:- Group 1: Traditional VPT JHU
- Group 2: SWAN VPT JHU
- Group 3: SWAN Motion Sick Dayton
- Group 4: Traditional Motion Sick Dayton
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Motion Sickness Patient Testimony for trial: Trial Name: NCT05622344 — N/A
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