Tokyo, Jan. 30 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000060513) titled 'Study on simulation methods for illusions during flight' on Jan. 29.
Study Type:
Interventional
Study Design:
Basic Design - Factorial
Randomization - Randomized
Blinding - Single blind -participants are blinded
Control - Placebo
Primary Sponsor:
Institute - Aviation Safety and Aeromedical Research Group
Condition:
Condition - Healthy Adults
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To investigate effective mithods for inducing flight illusions and spatial disorientation
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Galvanic Vestibular Stimulation (anode: right side), Visual Environment (Good)
Interventions/Control_2 - Galvanic Vestibular Stimulation (anode: right side), Visual Environment (Degraded)
Eligibility:
Age-lower limit - 20
years-old
=
Gender - Male and Female
Key inclusion criteria - Healthy adults aged between 20 and 40 years old
Individuals with unaided or corrected visual acuity of 1.0 or higher
Individuals can bring their regularly used contact lenses
Who consent to wearing pads moistened with saline solution, applying gel to the head, and wiping these off with a towel upon leaving
Native language is Japanese
Individuals with experience using commercial flight simulators
Key exclusion criteria - Pregnant or may be pregnant women
History of migraine, paroxysmal disorders, or epilepsy
Abnormalities on the scalp where electrodes will be attached
Metal implants in the body
Electroconvulsive therapy or transcranial direct current stimulation (tDCS) is clinically contraindicated
Adverse reactions to electrical stimulation
Surgical procedures involving the brain or spinal cord
Eye surgery or ocular diseased
Ear surgery or ear diseases
Smokers
Prone to simulator sickness or screen-induced nausea
Currently taking medication
Regularly wear glasses
Target Size - 10
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 12 Month 16 Day
Date of IRB - 2025 Year 12 Month 15 Day
Anticipated trial start date - 2026 Year 01 Month 16 Day
Last follow-up date - 2026 Year 03 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000069213
Disclaimer: Curated by HT Syndication.
