The Effectiveness of Cognitive Training for Digital Biomarkers: Evidence From the Urban and Rural Area
Smartphone-based cognitive training
Mental Disorders+1
+ Cognition Disorders
+ Neurocognitive Disorders
Diagnostic Study
Summary
Study start date: October 20, 2023
Actual date on which the first participant was enrolled.This study focuses on improving the understanding and availability of cognitive training for older adults living in rural areas, particularly to help with early detection and prevention of dementia. Current research suggests that dementia is more common in rural settings, but access to cognitive training is limited due to geographic and resource constraints. Digital biomarkers, which are non-invasive methods of monitoring health changes, offer a promising solution for early detection of cognitive decline. However, there is limited evidence on their effectiveness in rural populations. This study aims to explore how well digital biomarkers work in assessing cognitive function and how accessible cognitive training can be made for seniors in these areas. Participants in this study will engage in cognitive training exercises, which could be delivered through digital platforms, making it easier for those in remote locations to participate. The study will observe changes in cognitive function through these non-invasive digital biomarkers to determine their effectiveness. By prioritizing the autonomy and preferences of older adults, the study seeks to encourage successful health behavior changes. Although the study does not list specific risks or benefits, its innovative approach aims to bridge the gap in dementia care between urban and rural communities, potentially leading to better preventative strategies and resource distribution.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.90 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Diagnostic Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 60 to 95 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives