Suspended

The Effectiveness of Cognitive Training for Digital Biomarkers: Evidence From the Urban and Rural Area

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What is being tested

Smartphone-based cognitive training

Other
Who is being recruted

Mental Disorders+1

+ Cognition Disorders

+ Neurocognitive Disorders

From 60 to 95 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Diagnostic Study

Interventional
Study Start: October 2023
See protocol details

Summary

Principal SponsorTaipei Medical University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleThe Effectiveness of Cognitive Training for Digital Biomarkers: Evidence From the Urban and Rural Area
NCT06090942
Principal SponsorTaipei Medical University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

90 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Diagnostic Study

Diagnostic studies focus on improving how we detect or confirm a disease. They test new tools or techniques that could provide faster or more accurate diagnoses.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Mental DisordersCognition DisordersNeurocognitive DisordersCognitive Dysfunction

Criteria

3 inclusion criteria required to participate
At least 60 years of age, Can communicate in Chinese (Taiwanese)

Bring your own mobile device with Internet access.

Can act alone without physical impairment;full score of basic activities of daily living scale and instrumental activities of daily living scale.

5 exclusion criteria prevent from participating
Dementia diagnosed by a physician and in compliance with ICD-10

Physician diagnosed with significant mental illness or communication impairment

Participated in other cognitive training studies within the past year

Medical conditions associated with rapid functional and cognitive decline

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Smartphone-based cognitive training

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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