ClinicalTrials.gg
Not yet recruitingNCT07064382Updated Jul 14, 2025

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

An interventional study of VR-based multi-dimensional intervention in Dementia, Sleepiness and Mental Health, sponsored by Hong Kong University of Science and Technology. Not yet recruiting. Open to participants aged 60 Years to 120 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-14.

Primary conditionAlzheimer DiseaseRegistry: DementiaReclassifiedWhy we changed it
Registry
Dementia — the first condition term the registry derived for this study.
ClinicalTrials.gg
Alzheimer Disease
Why
  1. The study's listed conditions name Alzheimer Disease, a narrower term within Dementia.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Hong Kong University of Science and Technology · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
60 Years to 120 Years
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Dementia
  • Sleepiness
  • Mental Health
  • Alzheimer Disease

Browse trials for

03

In context

Alzheimer Disease Reclassified

3,965 studies on the registry are indexed under Alzheimer Disease; 926 are open to participants now.

This study's planned enrollment of 60 is below the median of 70 across 3,019 interventional studies indexed under Alzheimer Disease.

Browse Alzheimer Disease studies →

Lead sponsor

Hong Kong University of Science and Technology is the lead sponsor of 10 studies on the registry; 6 are open to participants now.

Compared within Alzheimer Disease, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Dementia. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
60 Years to 120 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • older adults

Exclusion criteria

Exclusion Criteria:

  • cannot attend physical activity like pedalling rehabilitation bike
  • other health issues (assessed by health professionals)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • No intervention
    control

    usual care

  • Experimental
    VR-based intervention

    Provide VR-based multi-dimensional intervention

    Device: VR-based multi-dimensional intervention

Interventions

  • DeviceVR-based multi-dimensional intervention

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

06

What researchers measure

Primary outcomes

  1. Spatial cognition

    mental rotation task,higher score means stronger spatial ability

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

  2. Spatial cognition

    money road map test, higher score means stronger spatial ability

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

  3. Spatial cognition

    building memory test, higher score means stronger spatial ability

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

  4. Spatial cognition

    corsi, , higher score means stronger spatial ability

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

  5. Spatial cognition

    digit span, higher score means stronger spatial ability

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

Secondary outcomes

  1. mental health

    UCLA loneliness, higher score means more loneliness

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

  2. mental health

    Positive and Negative Affect Schedule , 2 subscare, one is for positive, higher score means more positive affects, one is for negative, higher score mean more negetive affects

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

  3. mental health

    The World Health Organization-Five Well-Being Index (WHO-5), higher score means better mental well-being

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

Other outcomes

  1. Sleepiness

    Effects on sleepiness, measured by The Pittsburgh Sleep Quality Index (PSQI)

    Time frame: pre-intervention, after 4 weeks, 8 weeks, 12 weeks, 16 weeks, 3 months, 6 months, 1 year, 2 year, 3 year

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Personal identity and health metrics are restricted and confidentially saved.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jul 2025; primary completion for Jun 2028, 35 months later.

Of 882 non-industry interventional studies with no phase under Alzheimer Disease, half reached primary completion within 30 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 51. This study's planned 35 months is above that.

Counting every sponsor, half of 959 studies reached it within 29 months; a quarter within 15 and three quarters within 51.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 14, 2025
First posted
Jul 14, 2025
StartEst.
Jul 15, 2025
Primary completionEst.
Jun 15, 2028
CompletionEst.
Jun 15, 2028
Last update
Jul 14, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07064382
Lead sponsor
Hong Kong University of Science and Technology
Responsible party
GE LIN KAN (Professor, Hong Kong University of Science and Technology) — Principal investigator
First posted
Jul 14, 2025
Start date
Jul 15, 2025 (estimated)
Primary completion
Jun 15, 2028 (estimated)
Completion
Jun 15, 2028 (estimated)
Last update
Jul 14, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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