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User Satisfaction and Usefulness of a Virtual Reality–Based Program for Patients with Mild Cognitive Impairment

Assessing Satisfaction and Perceived Usefulness of the Cognitive Training Effects of the MIND STRONG VR Program Among MCI Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011198
Enrollment
20
Registered
2025-11-24
Start date
2025-08-22
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

None listed

Interventions

None listed

Sponsors

Kangdong Sacred Heart Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adults aged 60–90 years diagnosed with amnestic Mild Cognitive Impairment (MCI). 2. Presence of a subjective memory complaint reported by the patient or a caregiver. 3. Objective cognitive impairment, including memory, on neuropsychological testing relative to age- and education-adjusted norms. 4. Preserved global cognitive function. 5. No impairment in activities of daily living. 6. Not meeting criteria for dementia, as determined by a clinical physician. 7. Able to provide voluntary informed consent after receiving a full explanation of the study and demonstrating comprehension of its contents.

Exclusion criteria

Exclusion criteria: 1. Any severe, progressive, or unstable medical condition that could place the patient at risk. 2. Any medical or neurological condition that could account for cognitive impairment (e.g., abnormal thyroid function, vitamin B12 or folate deficiency, post-traumatic conditions, Huntington’s disease, multiple sclerosis, cerebral palsy, encephalitis, meningitis, or other disorders involving the central nervous system). 3. Any other diagnosis—other than depression—including major neurodegenerative diseases (e.g., dementia with Lewy bodies, frontotemporal dementia), schizophrenia, bipolar disorder, or other major psychiatric disorders per DSM-5 (e.g., autism spectrum disorder, severe obsessive–compulsive disorder). 4. Current uncontrolled seizure disorder. 5. History of traumatic brain injury within the past 3 years with loss of consciousness =1 hour or requiring hospitalization. 6. Hearing or visual impairment that could interfere with performance of trial requirements. 7. Considered by the investigator to be otherwise unsuitable for study participation.

Design outcomes

Primary

MeasureTime frame
Survey of Participant Satisfaction

Secondary

MeasureTime frame
Change in Total Score on the Korean Version of the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD-K);Change in Total Score on the Subjective Memory Complaints Questionnaire (SMCQ);Change in Total Score on the Geriatric Depression Scale (GDS)

Countries

Korea, Republic of

Contacts

Public ContactYeo Jin Kim

Kangdong Sacred Heart Hospital

yjhelena@hanmail.net+82-2-2224-2206

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026