Skip to content

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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008288
Enrollment
90
Registered
2023-03-14
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : One randomized subject performs one of three groups (forest VR with mindfulness, forest VR, and urban VR). Single intervention Each VR program takes about 20 to 30 minutes to complete t

Sponsors

Hallym University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (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.

Exclusion criteria

Exclusion criteria: (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

Design outcomes

Primary

MeasureTime frame
K-POMS;Heart Rate Variability;Electroencephalogram;Five Factor Mindfulness Scale -Short version;Korean Multidimensional Assessment of Interoceptive Awareness;functional near-infrared spectroscopy;State-Trait Anxiety Inventory -1;Korean Center for Epidemiological Studies-Depression Scale;Korean Pittsburgh Sleep Quality Index;Korean Obsessive-Compulsive Inventory Revised;Hamilton Anxiety Rating Scale;State-Trait Anxiety Inventory -2

Secondary

MeasureTime frame
Korean Toronto Mindfulness Scale;visual analog scale(Calm, anxiety)

Countries

Korea, Republic of

Contacts

Public ContactSangkyu Nam

Hallym University

skatkdrb11@hanmail.net+82-33-240-5174

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026