Clinical Trial: Investigating Behavioral Changes Among Older Adults in Response to Personalized Interventions Aimed at Enhancing Cognitive Reserve (Japan)

Tokyo, Aug. 14 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058785) titled 'Development of tailor-made behavior modification program based on cognitive function simulation, main study' on Aug. 13.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Open -no one is blinded Control - No treatment

Primary Sponsor: Institute - Keio University

Condition: Condition - Healthy adults over the age of 65 Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - This exploratory study aims to investigate the extent to which the use of a cognitive reserve simulation app, in addition to educational interventions for dementia prevention, promotes behavior change toward dementia-preventive actions among healthy older adults with a low risk of dementia. The study will also examine the use of cognitive training tools and the duration of sustained behavioral changes. Basic objectives2 - Others

Intervention: Interventions/Control_1 - The cognitive reserve simulation app will be used once at baseline. Interventions/Control_2 - The cognitive reserve simulation app will not be used at baseline.

Eligibility: Age-lower limit - 65 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - 1. Individuals aged 65 years or older 2. Individuals who have never been diagnosed with dementia 3. Individuals who have provided written informed consent to participate in this study 4. Individuals who are able to use a smartphone or tablet with access to the internet Key exclusion criteria - Participants who meet any of the following criteria will be excluded from this study 1. Individuals who have difficulty responding to assessment scales or operating a tablet device 2. Individuals with an MMSE score of 23 or lower 3. Individuals deemed unsuitable for participation in this study by the principal investigator or co-investigators Target Size - 200

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 04 Month 30 Day Anticipated trial start date - 2025 Year 08 Month 19 Day Last follow-up date - 2026 Year 03 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067149

Disclaimer: Curated by HT Syndication.