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Not yet recruiting NCT07064382

VR-based Multi-dimensional Intervention on Cognitive Function, With AI-agents

No phase Interventional Dementia Sleepiness Mental Health Alzheimer Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: VR-based multi-dimensional intervention.
Who it may be relevant to
Registry conditions: Dementia, Sleepiness, Mental Health, Alzheimer Disease. Basic parameters: 60 years — 120 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

VR-based Multi-dimensional Intervention on Cognitive Function and Well-beings

Overview

Virtual Reality-based multi-dimensional intervention for cognition and well-being will be provided to older adults, with AI-agents. The digital health intervention include physical activity, gamification, cognitive trainings. Cognition, like memory, spatial function, sleepiness and mental health will be studied as outcomes.

Detailed description

In order to study the cognitive function and well-beings, qualitative methods (like questionnaires, interviews, focus groups) and quantitative methods (like ppg, ecg, eyetracker, eeg) will be used to collect data for analysis.

Interventions

  • Device VR-based multi-dimensional intervention
    VR-based multi-dimensional intervention, including LLMs, AI-agents

Primary outcome measures

  • Spatial cognition [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]
  • Spatial cognition [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]
  • Spatial cognition [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]
  • Spatial cognition [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]
  • Spatial cognition [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]
Secondary outcome measures (3)
  • mental health [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]
  • mental health [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]
  • mental health [Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year]

Eligibility criteria

Inclusion criteria

  • older adults

Exclusion criteria

  • cannot attend physical activity like pedalling rehabilitation bike
  • other health issues (assessed by health professionals)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07064382 · MiM20250101

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗