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RECRUITING
NCT07033468
NA

The Feasibility and the Efficacy of the Full-immersive Virtual Reality Cognitive Training in Patients With Mild or Moderate Dementia

Sponsor: Chang Gung Memorial Hospital

View on ClinicalTrials.gov

Summary

This project will explore the feasibility and efficacy of the fully immersive virtual reality leisure cognitive training tool developed by Chang Gung University in patients with mild to moderate dementia. The feasibility study will assess the feasibility and emotion-related indicators of 10 patients before and after a single training session. The efficacy study is planned to adopt a crossover randomized controlled trial, recruiting 30 patients for 15 sessions, each lasting 65 minutes, conducted three times a week. The assessment will include tests on the primary variable of cognitive function and secondary variables such as activities of daily living, quality of life, emotion, clinical symptoms, etc.

Key Details

Gender

All

Age Range

55 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2024-08-01

Completion Date

2027-07-31

Last Updated

2025-06-24

Healthy Volunteers

No

Interventions

DEVICE

VR-WLC

First, conduct the Virtual Reality (VR) training activity. After the evaluation is completed, proceed to the Waitlist Control (WLC) session, approximately 5 to 10 weeks later.

DEVICE

CTL-VR

First, conduct the Control (CTL) session for approximately 5 to 10 weeks. After the evaluation is completed, proceed to the Virtual Reality (VR) training activity.

Locations (1)

Tucheng Hospital, New Taipei City, commissioned and operated by Chang Gung Medical Foundation.

New Taipei City, Taiwan