Culturally Familiar Nostalgic VR Cognitive Training for Older Adults
The Benefits of Nostalgia-Based Virtual Reality Brain Health Interventions on Nostalgia Tendencies, Life Satisfaction, Psychological Well-Being, Depression Levels, and Cognitive Function in Older Adults
1 other identifier
interventional
64
1 country
1
Brief Summary
This randomized controlled trial investigates the effects of a nostalgia-based cognitive training intervention delivered via Virtual Reality (VR) on emotional well-being and cognitive functioning among community-dwelling older adults (≥65 years) in northern Taiwan, specifically targeting those with mild cognitive impairment (MCI) or mild dementia. The study, conducted at National Taiwan Normal University, aims to assess whether engaging older adults in nostalgic VR experiences can enhance nostalgia proneness, life satisfaction, and psychological well-being, while also reducing depressive symptoms and improving cognitive functions. Participants who meet inclusion criteria (aged 65+, capable of communicating in Mandarin or Taiwanese, without severe psychiatric conditions, with sufficient vision/hearing) will be randomly assigned to either the experimental group receiving the "Brain Health Nostalgic VR Program" or a control group engaged in routine weekly activities. Each session, scheduled twice weekly, spans 25-35 minutes in total, including setup, support, and breaks, while the actual VR usage time is 15-25 minutes depending on individual tolerance. Research staff will provide close support and safety monitoring during all sessions. Pre- and post-intervention outcomes will be measured using standardized assessments: Southampton Nostalgia Scale (SNS), Short-Form Life Satisfaction Index (LSI-SF), Geriatric Depression Scale (GDS-15), Short-Form Chinese version of Ryff's Psychological Well-being Scale (PWB-18), and the Montreal Cognitive Assessment Taiwan Version (MoCA-T). The study emphasizes participant safety and data confidentiality throughout its duration. Findings aim to demonstrate VR's potential as a non-invasive, preventive strategy for cognitive decline and mental health enhancement among older populations.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 29, 2025
CompletedFirst Submitted
Initial submission to the registry
May 7, 2025
CompletedFirst Posted
Study publicly available on registry
May 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2026
CompletedApril 21, 2026
April 1, 2026
10 months
May 7, 2025
April 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Cognitive Function Assessed by MoCA-T
Cognitive function will be measured using the Montreal Cognitive Assessment - Taiwan Version (MoCA-T), a validated tool for detecting mild cognitive impairment (MCI) and early dementia. The MoCA-T assesses multiple domains including memory, attention, executive function, language, and visuospatial skills. Score range: 0-30 Interpretation: Higher scores indicate better cognitive functioning. For the Taiwanese version, a cutoff score of 23/24 has been suggested as the optimal threshold for distinguishing MCI patients from cognitively normal controls.
Baseline, post-intervention (up to 8 weeks), and 3 months post-intervention
Secondary Outcomes (4)
Change in Nostalgia Proneness Assessed by Southampton Nostalgia Scale (SNS)
Baseline, post-intervention (up to 8 weeks), and 3 months post-intervention
Change in Depression Symptoms Assessed by GDS-15
Baseline, post-intervention (up to 8 weeks), and 3 months post-intervention
Change in Psychological Well-being Assessed by PWB-18
Baseline, post-intervention (up to 8 weeks), and 3 months post-intervention
Change in Life Satisfaction Assessed by LSI-SF
Baseline, post-intervention (up to 8 weeks), and 3 months post-intervention
Study Arms (2)
Nostalgia-Based VR Cognitive Training
EXPERIMENTALParticipants in this arm will receive the "Brain Health Nostalgic VR Program," a culturally grounded virtual reality intervention integrating nostalgic elements representative of Taiwanese culture (e.g., old photographs, household objects, traditional media, and familiar scenarios) with interactive cognitive training. The training targets seven domains: attention, imagination and creativity, observation, memory, reasoning, reading comprehension, and thinking. Each session spans 25-35 minutes in total, including setup, support, brief reflection, and closure, while the actual VR usage time is 15-25 minutes depending on individual tolerance. The intervention is conducted in 12 sessions, scheduled in principle twice weekly, at the participant's day-care center, with full assistance and monitoring by the research team.
Routine Weekly Activities
NO INTERVENTIONParticipants in this arm will continue with their routine weekly activities provided by their respective long-term care facilities. These activities may include light physical exercise, social engagement, passive entertainment (e.g., watching TV), or unstructured leisure. No structured cognitive training or VR-related content will be administered. This arm serves as a control group for comparison with the experimental group receiving the nostalgia-based VR intervention.
Interventions
The "Brain Health Nostalgic VR Program" is a culturally tailored virtual reality intervention integrating nostalgic content from Taiwanese culture (e.g., vintage photographs, familiar objects, historical TV clips, traditional settings) with interactive cognitive training tasks. The program targets seven cognitive domains: attention, imagination and creativity, observation, memory, reasoning, reading comprehension, and thinking. Each session spans 25-35 minutes, with 15-25 minutes of actual VR use based on participant tolerance, each participant will use VR for no more than 30 minutes per session before taking a break. Participants receive 12 sessions, scheduled in principle twice weekly. The intervention is delivered individually at the participant's day-care center, with researcher support provided throughout.
Eligibility Criteria
You may qualify if:
- Age 65 years or older
- Able to communicate in Mandarin or Taiwanese
- Capable of wearing and operating a VR headset and handheld controllers
- Sufficient vision and hearing to interact with VR content (assistive devices permitted)
- Able to provide informed consent or have a legal guardian provide consent
You may not qualify if:
- Diagnosis of severe dementia or advanced neurodegenerative disease
- Severe psychiatric disorders (e.g., schizophrenia, bipolar disorder)
- Major visual or auditory impairments that would interfere with VR use, even with assistive devices
- Unconsciousness, inability to stay awake or focused for the session duration Inability to comply with study protocol or scheduled sessions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Taiwan Normal University
Taipei, Taipei City, 10610, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Jong-Long Guo, PhD
National Taiwan Normal University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 7, 2025
First Posted
May 15, 2025
Study Start
April 29, 2025
Primary Completion
February 10, 2026
Study Completion
March 30, 2026
Last Updated
April 21, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
De-identified individual participant data (IPD) will be available after publication of the main trial results in an international peer-reviewed journal. Access requires a formal request to the corresponding author and approval. Shared data will include variables related to primary and secondary outcomes (e.g., demographics, cognitive function, well-being, depression, and life satisfaction). Data will be provided for academic, non-commercial research only, beginning 6 months after publication and up to 3 years thereafter. Qualified researchers must submit a sound proposal; upon approval, data will be securely transferred electronically.