Clinical Trials Logo

Clinical Trial Summary

Chronic motion sensitivity refers to a sensation of unwellness caused by physical or discerned motion and has a prevalence of 28% in the general population and it is more common in women (27.3%) compared to men. The investigators theorize that individuals with chronic motion sensitivity will have an impaired inner ear reflex and will be less physically active. Hence, the purpose of this study is to; 1. Determine whether the function of an inner ear reflex is different between young adults with/without chronic motion sensitivity 2. Assess relationships between reflex function and balance in young adults with/without CMS 3. Assess relationships between physical activity and balance in young adults with/without CMS.


Clinical Trial Description

Chronic motion sensitivity (CMS), also known as motion sickness, refers to a sensation of unwellness caused by physical or discerned motion. CMS has a prevalence of 28% in the general population and it is more common in women (27.3%) compared to men. Based on established evidence that individuals with chronic motion sensitivity demonstrate impaired postural stability with vestibular system impairment adjudged to be an inciting stimulus for chronic motion sensitivity, and individuals who practiced more physical and sporting activities have less motion sickness susceptibility than individuals who did not, the investigators theorize that individuals with chronic motion sensitivity will have an impaired inner ear reflex, causing them to be more reliant on other sensory systems like their muscles and joints, and their vision, we also theorize that individuals who are physically active will be less susceptible to chronic motion sensitivity. The purpose of this study is to; 1. Determine whether the function of an inner ear reflex is different between young adults with/without chronic motion sensitivity 2. Assess relationships between reflex function and balance in young adults with/without CMS 3. Assess relationships between physical activity and balance in young adults with/without CMS. Participants between the age of 20 and 40 with and without a self-reported history of chronic motion sensitivity (i.e, experiencing nauseousness and/or dizziness during while using various means of transportation such as, car, train, bus, boat, and airplane and/or, recreational fun-fair rides and/or when exposed to conflicting visual images). Participants will be excluded if they report a medical diagnosis of central nervous system disorder, impaired cervical spine range of motion, migraines, seizure disorder, vestibular dysfunction, or any musculoskeletal dysfunction that can limit their participation in the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06128707
Study type Observational [Patient Registry]
Source Loma Linda University
Contact
Status Recruiting
Phase
Start date September 30, 2023
Completion date March 23, 2024

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT04196933 - Analysis of Vestibular Compensation Following Clinical Intervention for Vestibular Schwannoma N/A
Completed NCT05611814 - Preliminary Evaluation of an Osteopathic Manipulative Treatment (OMT) to Prevent Motion Sickness Symptoms N/A
Recruiting NCT06106256 - Three-Axis Wearable Adaptive Vestibular Stimulator N/A
Completed NCT02839135 - A Comparative Bioavailability and Adhesion Performance Study, Comparing a New Scopolamine Transdermal Delivery System Formulation to the Currently Established Reference Transdermal Delivery System in Healthy Adult Participants. Phase 1
Completed NCT04420949 - Sensory Training for Visual Motion Sickness N/A
Completed NCT04184115 - Nasal Gel for the Prevention and Treatment of Nausea Associated With Motion Sickness Phase 3
Completed NCT03988530 - Prevention and Treatment of Nausea Associated With Motion Sickness in Senior Subjects Phase 3
Terminated NCT04219982 - DPI 386 Nasal Gel for the Prevention of Nausea Associated With Motion Sickness Phase 2/Phase 3
Terminated NCT02155309 - Pharmacokinetic and Efficacy Profile Intranasal Scopolamine Spray Phase 2/Phase 3
Completed NCT04947423 - Nasal Gel for the Prevention of Nausea and Vomiting Associated With Motion Phase 3
Recruiting NCT05903924 - Motion Serifos: A Study to Investigate the Efficacy of Tradipitant in Participants Affected by Motion Sickness Phase 3
Recruiting NCT04999449 - Nebulizer Delivery of Intranasal Scopolamine Phase 1
Recruiting NCT05886660 - Combination of Intranasal Scopolamine and Sensory Augmentation to Mitigate G-transition Induced Motion Sickness and Enhance Sensorimotor Performance Phase 2
Completed NCT03755596 - Clinical Evaluation of the Use of Ginger Extract in the Management of Motion Sickness Phase 4
Recruiting NCT05628220 - Motion Sickness Desensitization Using VR N/A
Recruiting NCT06138613 - Motion Delos: An Open Label Safety and Efficacy of Tradipitant in Participants Affected by Motion Sickness Phase 3
Completed NCT04327661 - Motion Syros: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion Sickness Phase 3
Completed NCT06232785 - Gynecologic Endoscopic Surgery of Female Motion Sickness Patients Phase 4
Completed NCT06056622 - Motion Sickness Rehabilitation for Virtual Reality N/A
Withdrawn NCT04331561 - Sensory Training for Orientation and Balance N/A