Geneva, Aug. 29 -- International Clinical Trials Registry received information related to the study (JPRN-UMIN000058785) titled 'Development of tailor-made behavior modification program based on cognitive function simulation, main study' on Aug. 13.
Study Type: Interventional
Study Design:
Parallel Randomized
Primary Sponsor: Keio University
Condition:
Healthy adults over the age of 65
Intervention:
The cognitive reserve simulation app will be used once at baseline.
The cognitive reserve simulation app will not be used at baseline....
Recruitment Status: Not Recruiting
Phase: Not selected
Date of First Enrollment: 2025/08/19
Target Sample Size: 200
Countries of Recruitment:
Japan
To know more, visit https://center6.umin....