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An exploratory study on fostering daily conversation habits centered on perspective-taking and time orientations for maintaining cognitive health

Development of cognitive intervention method through group conversation - Development of cognitive intervention method through group conversation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057738
Enrollment
120
Registered
2025-04-29
Start date
2025-06-03
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

Healthy older and younger adults and persons with cognitive impairments (including long-term care users)

Interventions

A group conversation consisting of about 5 people is conducted. Before the session, participants are asked to take photos of a given theme with their smartphones or tablets and upload them to the appl

Sponsors

RIKEN
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Persons who can intervene and perform necessary tests on the specified date -Persons who can provide their consent.

Exclusion criteria

Exclusion criteria: -Persons who have difficulty participating due to serious illness (eg., hospitalization)

Design outcomes

Primary

MeasureTime frame
Verbal fluency test *Evaluation Pre, post-intervention, and once a year during the intervention

Secondary

MeasureTime frame
Interpersonal Reactivity Index Social Comparison Orientation scale Zimbardo Time Perspective Inventory Personal Values Questionnaire II Lubben Social Network Scale Kihon Checklist World Health Organization-Five Well-Being Index UCLA Loneliness Scale NEO Five-Factor Inventory WMS-R Logical Memory I and II Mini-Mental State Examination Montreal Cognitive Assessment National Center for Geriatrics and Gerontology-Functional Assessment Tool Blood biomarkers *Evaluation Pre, post-intervention, and once a year during the intervention (For PVQ-II and MMSE, only at pre- and post-intervention. Due to scheduling constraints, NEO-FFI will be measured at two time points during the intervention period, preferably as close as possible to the baseline and endpoint. For blood biomarkers, measurements will be taken at a time point during the intervention period as close as possible to baseline, annually during the intervention, and after the intervention.) As implementation outcomes, dropout rate (acceptability) and the number of questions asked per conversation session (adherence) are recorded.

Countries

Japan

Contacts

Public ContactMihoko Otake-Matsuura

RIKEN Center for Advanced Intelligence Project

mihoko.otake@riken.jp0362252482

Outcome results

None listed

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