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Virtual reality I-ADL training for mild dementia: a study of efficacy and feasibility

Virtual reality I-ADL training for mild dementia: a study of efficacy and feasibility

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007341
Enrollment
28
Registered
2022-06-02
Start date
2022-06-09
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : Intervention period: 6-8 weeks Experimental group: Conventional cognitive training, 30-45 minutes/session, once a week + VR-based IADL training, 30 minutes/session (total 10 sessions) Contro

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients with mild cognitive impairment or mild dementia with K-MMSE = 18 or GDS score of 2-6 - Patients with low risk of falls (41-56 points on the berg balance scale) - Patients with at least one upper limb muscle strength of grade 4 or higher in the manual muscle test

Exclusion criteria

Exclusion criteria: - patients with a visual or auditory impairment - patients with difficulties in understanding the training instructions - patients with dizziness - other reasons that the researcher determined to be inappropriate for participation in this study

Design outcomes

Primary

MeasureTime frame
CERAD-K, S-IADL, Beck Depression Inventory

Secondary

MeasureTime frame
Measurements in VR Program (performance time, number or errors, etc) ;Self-Questionnaire for Acceptability, Adherence ;Presence scale

Countries

Korea, Republic of

Contacts

Public ContactCho Rong Bae

Asan Medical Center

june7258318@hanmail.net+82-2-3010-3525

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 7, 2026