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A preliminary study for the calculation of effect size on cognitive and physical functions according to cognitive intervention methods

A preliminary study for the calculation of effect size on cognitive and physical functions according to cognitive intervention methods

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009647
Enrollment
36
Registered
2024-07-26
Start date
2024-07-15
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

None listed

Interventions

Medical Device : It consists of three conditions: computerized cognitive training once in 20 minutes (A intervention), transcranial direct current stimulation (tDCS), once in 20 minutes (B interventio

Sponsors

Kumoh National Institute of Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Elderly people in the community aged 55 to 84 years old 2. Subjects with mild cognitive decline with a score of 25 or less in the Korean version of the Montreal Cognitive Assessment (K-MoCA)

Exclusion criteria

Exclusion criteria: 1. A person who has difficulty walking independently due to serious visual field defects, fractures, brain diseases, etc 2. A person who had a history of musculoskeletal system that may cause problems with physical function, such as fractures, within six months prior to recruitment 3. A person who is difficult to understand and cannot voluntarily consent to participate in the study due to severe cognitive decline 4. A person who has difficulty in accurate evaluation of functions due to failure to read Hangul 5. A person who is accompanied by a serious mental illness such as schizophrenia and bipolar disorder 6. Non-invasive brain stimulation intervention non-conforming persons – implantation of medical devices in the body such as artificial heartbeats, insertion of skull metal, injury to skin at the electrode attachment area, history of epilepsy, pregnant women and lactating women

Design outcomes

Primary

MeasureTime frame
N-back Test

Secondary

MeasureTime frame
Cognitive Function Assessment;Physical Function Assessment

Countries

Korea, Republic of

Contacts

Public ContactJungsoo Lee

Kumoh National Institute of Technology

jungsoo0319@gmail.com+82-54-478-7784

Outcome results

None listed

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