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Behavioural Intervention
Vestibulo-Ocular Reflex Therapy for Mal de Debarquement Syndrome
N/A
Waitlist Available
Led By Sergei Yakushin, PhD
Research Sponsored by Icahn School of Medicine at Mount Sinai
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and 6 month follow up
Awards & highlights
Study Summary
This trial aims to find a way to stop the symptoms of MdDS by eliminating the trigger and minimizing symptoms.
Eligible Conditions
- Mal de Debarquement Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and 6 month follow up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 6 month follow up
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Subjective Symptoms Self-report of Overall Severity
Secondary outcome measures
Dizziness Handicap Inventory (DHI) Questionnaire
VOR Direct Pathway Gain
VOR Indirect Pathway Coupling Gain
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: Vestibulo-ocular reflex (VOR)Experimental Treatment1 Intervention
Treatment by re-adaptation of the vestibulo-ocular reflex (VOR) for participants with motion triggered MdDS
Group II: Habituation of velocity storageExperimental Treatment1 Intervention
Participants with motion triggered MdDS
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
re-adaptation of the vestibulo-ocular reflex
2020
N/A
~50
Habituation of velocity storage of the vestibulo-ocular reflex
2020
N/A
~50
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Who is running the clinical trial?
Icahn School of Medicine at Mount SinaiLead Sponsor
858 Previous Clinical Trials
524,239 Total Patients Enrolled
National Institute on Deafness and Other Communication Disorders (NIDCD)NIH
328 Previous Clinical Trials
178,258 Total Patients Enrolled
Sergei Yakushin, PhDPrincipal Investigator - Icahn School of Medicine at Mount Sinai
Icahn School of Medicine at Mount Sinai
1 Previous Clinical Trials
200 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Vestibulo-ocular reflex (VOR)
- Group 2: Habituation of velocity storage
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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