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Effectiveness of tablet-based cognitive training

Effectiveness of tablet-based cognitive training - Effectiveness of tablet-based cognitive training

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040051
Enrollment
150
Registered
2020-04-04
Start date
2020-04-04
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Mood disorder Anxiety disorder Autism spectrum disorder Attention deficit hyperactivity disorder Mild cognitive impairment Normal healthy control

Interventions

We conduct a maximum of 20 cognitive training at a pace of 4-5 days per week.

Sponsors

Keio University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Patient group People who were diagnosed with mood disorder, anxiety disorder, ASD, ADHD, MCI in DSM-5 2 Healthy control group A healthy person without a history of mental illness

Exclusion criteria

Exclusion criteria: People who satisfies one of the following 1 Combined circulatory organ, liver, kidney, respiratory organs, blood, endocrine, central nervous system diseases, and person who was judged to be extremely unstable 2 Person who has history of head trauma or substance dependence 3 People with a history of epilepsy or generalized convulsions 4 For healthy control subjects, those who are diagnosed with developmental disorder

Design outcomes

Primary

MeasureTime frame
1 Clinical evaluation scale HAM-D, HAM-A, MADRAS, etc. 2 Neuropsychological examination TMT, BADS, CAT, CANTAB, etc.

Countries

Japan

Contacts

Public ContactBun Yamagata

Keio University School of Medicine Department of Neuropsychiatry

yamagata@a6.keio.jp03-5363-3971

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026