Effect of virtual reality training compared to conventional rehabilitation: A prospective, explorative, randomized crossover trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009624

Enrollment

Registered

2024-07-10

Start date

2024-09-11

Completion date

Unknown

Last updated

2026-01-27

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: Conducted for 4 weeks and again for 4 weeks after a 2-week of washout period Experimental group: 50 minutes / session, 2 sessions / week (20 minutes of VR based IADL training +

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Patients with mild cognitive impairment or mild dementia with GDS of 2 to 5 or MMSE standards of 16% or less - Patients with at least one upper limb muscle strength of grade 4 or higher in the manual muscle strength test

Exclusion criteria

Exclusion criteria: - patient with a visual or auditory impairment - patient with high risk of falls (40 points or less on the Berg balance scale of) - patient with difficulties in understanding the training instructions - patient with severe dizziness - other reasons that the researcher determined to be inappropriate for participation in this study

Design outcomes

Primary

Measure	Time frame
CERAD-K, S-IADL, Beck Depression Invenory, EQ-5D-5L	—

Secondary

Measure	Time frame
Measurements in VR Program (performance time, number of errors, etc);Self-Questionnaire for Acceptability, Adherence;Presence scale	—

Countries

Korea, Republic of

Contacts

Public ContactSeungwoo Cha

Asan Medical Center

miracleofs@naver.com+82-2-3010-3799

Outcome results