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Effectiveness of the Zenicog® Cognitive Rehabilitation Program for Older Adults with Mild Cognitive Impairment: A Randomized Controlled Trial/A pilot study

Effectiveness of the Zenicog® Cognitive Rehabilitation Program for Older Adults with Mild Cognitive Impairment: A Randomized Controlled Trial/A pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008968
Enrollment
73
Registered
2023-11-21
Start date
2023-11-22
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

None listed

Interventions

Others : 1. During the intervention period, participants will perform 24 sessions of the Zenicog® program installed on a tablet PC within their home environment, over the course of 5weeks (one session

Sponsors

Catholic Kwandong University International St.Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) The research targets older adults, with an age restriction of 65 years and older. 2) Participants will be selected as older adults with cognitive impairment, based on a criterion of MMSE (Mini-Mental State Examination) scores within the range of 18 to 26 points.

Exclusion criteria

Exclusion criteria: Patients with limitations in using computerized devices due to visual, auditory, or motor impairments will be excluded. Individuals with a significant level of digital illiteracy, making it difficult to operate smart devices, will be excluded. Subjects with severe mental disorders (such as schizophrenia, bipolar disorder, etc.) or major depressive disorders (severe depression, secondary depression, etc.) that may impair cognitive assessment will be excluded. Individuals who are taking medications that could affect cognitive function will be excluded. 3-1) Users of dementia treatment drugs (acetylcholinesterase inhibitors like donepezil, galantamine, rivastigmine, etc.) will be excluded. 3-2) Central nervous system drugs: Antipsychotic medications, antidepressants, alcohol-related drugs (medications for alcohol addiction treatment), sedatives (tranquilizers, sedatives, benzodiazepine drugs, etc.). 3-3) Opioid drugs (e.g., oxycodone) will also result in exclusion.

Design outcomes

Primary

MeasureTime frame
Cognitive Function Indicator: Comprehensive Cognitive Indicator (K-MMSE2);Attention and Concentration (Trail making test A, Word-color test);Working Memory(Digit span, Visual span test);Executive Function (Trail Making Test B, Card Sorting Test);Psychological outcome measures: 1) Quality of Life Measure (EQ-5D-5L) 2) Self-esteem (Self Efficacy Scale) 3) Depression (Korean version of Center for Epidemiological Studies-Depression Scale, K-CES-D);Activities of Daily Living (ADL) measure: Seoul-Instrumental Activities of Daily Living (S-IADL);Electromyography Biomarkers

Secondary

MeasureTime frame
Psychological outcome measures: 1) Quality of Life Measure (EQ-5D-5L) 2) Self-esteem (Self Efficacy Scale) 3) Depression (Korean version of Center for Epidemiological Studies-Depression Scale, K-CES-D);Activities of Daily Living (ADL) measure: Seoul-Instrumental Activities of Daily Living (S-IADL);Usability Analysis: Usability Test (Development Questionnaire);Electromyography Biomarkers;Cognitive Function Indicator: Comprehensive Cognitive Indicator (K-MMSE2);Attention and Concentration (Trail making test A, Word-color test);Working Memory(Digit span, Visual span test);Executive Function (Trail Making Test B, Card Sorting Test)

Countries

Korea, Republic of

Contacts

Public Contacttaeksoo jeong

Catholic Kwandong University International St.Mary's Hospital

jeongtaeksoo8@gmail.com+82-32-290-3117

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Apr 30, 2026