Explore the Effects of Virtual Reality Natural Environment of Older People
NCT ID: NCT05803460
Last Updated: 2025-12-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
120 participants
INTERVENTIONAL
2023-04-07
2024-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Integration of VR and AR Dementia Prevention Health Education Progrom for Older Adults With Mild Cognitive Impairment
NCT06888986
Efficacy of VR Educational Program on Empathy and Attitudes Toward Dementia in Caregivers
NCT06072274
Exploring the Impact of Dementia Prevention Programs Using Robots as Intervention Tools on Community Elderly
NCT06984458
VR-Based Intervention for Caregiving Competence in Dementia
NCT06797180
Personalized Virtual Reality Naturalistic Scenarios in Cognitive Impairment
NCT05863065
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Virtual nature group: virtual reality experience of nature environment
virtual reality experience of nature environment; Participants watched a 20-minute video of a virtual natural environment filmed by researchers.
Experimental group: Virtual nature group
Participants will experience the virtual reality natural environment by the researcher for 20 minutes.The 360-degree panoramic natural environment scenes were from a natural park in Taipei City.Considering the elderly user experience, this study utilized standalone immersive virtual reality headset. Once wearing the goggles in a comfortable seated position, participants engaged in a 20-minute virtual reality environment experience.
Actual urban group: actual experience of city
actual experience of city; participants in the group engage in 20 minutes of seated meditation in a safe urban area.
Control group: Actual urban group
Participants will sit still for 20 minutes in a city environment.The urban environment is selected within the community's urban landscape.
Actual nature group: Actual experience of nature environment
actual natural environment; participants in this group engage in 20 minutes of seated meditation in a natural park.
Experimental group: Actual nature group
Participants will go to the park and sit still for 20 minutes.The natural environment site is the same as the video scenes used in the virtual natural environment intervention, located in a natural park in Taipei City.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Experimental group: Actual nature group
Participants will go to the park and sit still for 20 minutes.The natural environment site is the same as the video scenes used in the virtual natural environment intervention, located in a natural park in Taipei City.
Experimental group: Virtual nature group
Participants will experience the virtual reality natural environment by the researcher for 20 minutes.The 360-degree panoramic natural environment scenes were from a natural park in Taipei City.Considering the elderly user experience, this study utilized standalone immersive virtual reality headset. Once wearing the goggles in a comfortable seated position, participants engaged in a 20-minute virtual reality environment experience.
Control group: Actual urban group
Participants will sit still for 20 minutes in a city environment.The urban environment is selected within the community's urban landscape.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Cognitive function is normal (SPMSQ \>8)(The SPMSQ test was performed before the intervention to screen the cognitive function of the subjects).
3. The subjects can communicate in Chinese or Taiwanese.
Exclusion Criteria
2. Vision or hearing problems
3. Diseases transmitted by eyes or skin
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Yang Ming Chiao Tung University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Cheng-Chen Chou, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Nursing
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Yang Ming Chiao Tung University
Taipei, Taiwan, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
YM111067E
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.