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Verification of the effects of cognitive and oral function training using exergaming and dual tasks

Verification of the effects of cognitive and oral function training using exergaming and dual tasks - Verification of the effectiveness of cognitive and oral function training

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052749
Enrollment
46
Registered
2023-11-10
Start date
2023-12-01
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

Oral dysfunction/dementia

Interventions

Cognitive/oral function training Tablet operation only

Sponsors

Tohoku University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those who understand the purpose and content of this study and have obtained the necessary written consent to participate in the study.

Exclusion criteria

Exclusion criteria: (1) Those who have or are undergoing treatment for a disorder in their stomatognathic function. (2) Those who were diagnosed as needing dental treatment during the intervention period. (3) Persons who are judged to have difficulty in training due to ill-fitting dentures. (4) Denture users with three or more consecutive missing teeth. (5) Persons with Eichner classification B2-C3. (6) A person who lacks sufficient judgment ability. (8) Persons with a history of mental illness, diabetes, cranial nerve disease, or heart disease (heart disease). (9) Persons taking drugs that affect cognitive function (e.g. benzodiazepines, antidepressants, central nervous system drugs). (10) Her score on the MMSE-J (Mini Mental State Examination-Japanese), a screening test for dementia, is Those with 26 points or less. (11) Those who are currently participating in another study or who have participated in another study within 2 months before the start of the study. (12) Those who are unable to participate in the pre-test and post-test conducted before and after the intervention period. (13) Any other person deemed inappropriate.

Design outcomes

Primary

MeasureTime frame
Oral function (pronunciation function) and cognitive function (executive function, short-term memory, and working memory)

Countries

Japan

Contacts

Public ContactNobuhiro Yoda

Tohoku University Hospital

nobuhiro.yoda.e2@tohoku.ac.jp0227178369

Outcome results

None listed

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