Can a smartwatch boost care quality for seniors?
NCT ID NCT07579832
First seen Jun 25, 2026 · Last updated Aug 21, 2026 · Updated 2 times
Summary
This study will give 1,080 older adults with disabilities a smart wristband to wear for 8 weeks. The device tracks steps, heart rate, and fatigue, and shares data with caregivers and healthcare providers. Researchers want to see if this improves physical activity, daily functioning, and reduces caregiver stress.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Smart Wearable Wristband-Based Monitoring System
- What this could lead to
- If successful, this could show that wearable devices help improve physical activity and care coordination for older adults with disabilities, potentially reducing caregiver burden.
- What could go wrong
- This is an early-stage observational study without a control group, so results may not prove cause and effect. The wristband may be uncomfortable or difficult for some participants to use consistently.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 1,080 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Older adults with disabilities: * Aged ≥ 65 years. * Classified as CMS level 2-6 under Taiwan Long-Term Care Need Assessment. * Currently receiving at least one Long-Term Care 2.0 service (e.g., home care, home-based rehabilitation, or respite care). * Have normal cognitive function, or a Mini-Mental State Examination (MMSE) score ≥ 23 when cognitive screening is performed. * Own and are able to use a smartphone. * Willing to participate and provide written informed consent. * Family caregivers: * Have normal cognitive function, or a Mini-Mental State Examination (MMSE) score ≥ 23 when cognitive screening is performed. * Own and are able to use a smartphone. * Willing to participate and provide written informed consent. * Multidisciplinary rehabilitation professionals: * Employed or contracted by a home-based long-term care institution with at least three professional disciplines (e.g., physical therapists, occupational therapists, nurses, social workers). * Own and are able to use a smartphone. * Willing to participate and provide written informed consent. Exclusion Criteria: * Older adults with disabilities: * Severe acute medical conditions or unstable physiological status. * Severe cognitive impairment without a caregiver capable of assisting with questionnaires. * Not currently receiving any long-term care services. * Family caregivers: * Severe acute medical conditions or unstable physiological status. * Severe cognitive impairment without ability to complete questionnaires. * Not currently involved in long-term care services. * Multidisciplinary rehabilitation professionals: * Providing services exclusively in non-home-based settings (e.g., institutional or hospital-only care).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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National Center for Geriatrics and Welfare Research, National Health Research Institute
RECRUITINGHuwei, Yunlin City, 632007, Taiwan
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