Effect of Virtual Reality Program on Improvement of Psychological and Physiological Stress

Hallym University0 个研究点目标入组 90 人开始时间: 待定最近更新: 2023年4月4日

试验速览

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•(1) Men and women between the ages of 19 and under 65 years of age.
•(2) A person who can read and understand the subject's explanatory text and consent form, and has the level of language ability to respond to the questionnaire.
•(3) A person who voluntarily decided to participate in this clinical trial and gave written consent to the informed consent form and can participate in the entire clinical trial period.
•(4) Among psychiatric patients, including general subjects, those who reported a score of 14 or higher on the Perceived Stress Scale.
•(5) A person suffering from an anxiety disorder or a mood disorder.

•(1) Pregnant women, people with binocular vision impairment, mentally ill, or those with heart disease and other serious health problems.
•(2) To prevent the spread of contagious diseases (conjunctivitis), persons with contagious symptoms, infections or diseases, especially those with contagious symptoms or diseases of the eyes, skin or scalp.
•(3) Persons who have experienced severe dizziness, seizures, eye or convulsions or temporary loss of consciousness due to flashes or patterns.
•(4) Persons diagnosed with alcohol abuse and alcohol dependence
•(5) Those who have organic abnormalities in the brain, such as Parkinson's or glare-ray brain disease.
•(6) Those who have experience of substance abuse.
•(7) Persons with intellectual disabilities.
•(8) Those who have attempted suicide within 6 months of the screening date
•(9) In addition to the above, those who have clinically significant findings that the principal investigator or the person in charge medically judges to be inappropriate for this study

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