Health TrialsbyHealthPanel

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

ConditionsDementiaSleepinessMental HealthAlzheimer Disease
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60-120
SponsorHong Kong University of Science and Technology

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

older adults

Disqualifiers

cannot attend physical activity like pedalling rehabilitation bike

other health issues (assessed by health professionals)

Trial design

Design model

Parallel

Treatments tested in this trial

  • VR-based multi-dimensional intervention

    Device

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

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: controlNo intervention 0 interventions
Group B: VR-based interventionExperimental treatment 1 intervention

Trial outcomes

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

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

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Hong Kong University of Science and Technology

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: