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Quantitative Monitoring of Disability Care Quality for Long-Term Care Facilities 2

Quantitative Monitoring of Disability Care Quality for Long-Term Care Facilities 2

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07579832
Enrollment
1080
Registered
2026-05-12
Start date
2026-06-01
Completion date
2027-12-31
Last updated
2026-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Activities of Daily Living, Aged, Disabled Persons, Motor Activity

Brief summary

The goal of this clinical trial is to evaluate whether a smart wearable wristband-based care system can improve the quality of care and physical activity levels among older adults with disabilities receiving home-based care. The study population includes older adults with disabilities, their family caregivers, and multidisciplinary rehabilitation service providers. The main questions it aims to answer are: 1. Whether the use of a smart wearable wristband can improve functional performance, as measured by Activities of Daily Living (ADLs), Instrumental Activities of Daily Living (IADLs), and Integrated Care for Older People (ICOPE) assessments? 2. Whether the intervention can increase physical activity levels and improve overall care quality, while reducing caregiver burden and enhancing satisfaction? Participants will: 1. Wear a smart wearable wristband continuously for 8 weeks to record physical activity data, including step count, activity level, heart rate, and fatigue index. 2. Undergo assessments at baseline and after the 8-week intervention, including Activities of Daily Living (ADLs), Instrumental Activities of Daily Living (IADLs), Integrated Care for Older People (ICOPE), and the Chinese Version of the Physical Activity Scale for the Elderly (PASE-C). 3. Provide data on caregiver stress, satisfaction, and service utilization for the analysis of care quality.

Interventions

DEVICESmart Wearable Wristband-Based Monitoring System

The intervention consists of an 8-week use of a smart wearable wristband device. The device continuously collects physiological and physical activity data, including step count, activity level, heart rate, and fatigue index. The system provides feedback on activity patterns and supports care coordination among older adults with disabilities, family caregivers, and multidisciplinary professionals through a digital communication system. Data collected from the device will be used to monitor changes in physical activity among older adults with disabilities and to evaluate changes in care quality for family caregivers and multidisciplinary professionals before and after the intervention.

Sponsors

National Health Research Institutes, Taiwan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
Physical activity level (step count)Baseline (0 week) and after intervention (8 weeks)Step count in older adults with disabilities will be measured using a smart wearable wristband to assess changes in physical activity before and after the 8-week intervention.
Physical activity level (heart rate)Baseline (0 week) and after intervention (8 weeks)Heart rate in older adults with disabilities will be measured using a smart wearable wristband before and after the 8-week intervention.
Physical activity level (fatigue index)Baseline (0 week) and after intervention (8 weeks)Fatigue index in older adults with disabilities will be calculated using the algorithm embedded in the smart wearable wristband system and assessed before and after the 8-week intervention.
Caregivers stress (Scale title: Caregiver Burden/stress Scale)Baseline (0 week) and after intervention (8 weeks)Caregiver stress in family caregivers will be assessed using a validated caregiver burden/stress scale. The total score ranges from 0 to 36 and will be transformed to a 0-100 scale for analysis. A higher score indicates greater caregiver burden and stress.
Satisfaction with smart wearable wristband systemBaseline (0 week) and after intervention (8 weeks)Satisfaction with the smart care system will be assessed among multidisciplinary professionals using a structured satisfaction questionnaire. The questionnaire evaluates multiple domains, including usability, applicability, service quality, sustainability, and motivation. Responses are rated using a 5-point Likert scale ranging from very dissatisfied to very satisfied, with higher scores indicating greater satisfaction.

Secondary

MeasureTime frameDescription
Activities of daily living (Scale title: Activities of Daily Living)Baseline (0 week) and after intervention (8 weeks)Functional status in older adults with disabilities will be assessed using the Activities of Daily Living (ADL) scale. Scores range from 0 to 100, with higher scores indicating greater ability to perform activities of daily living.
Instrumental activities of daily living (Scale title: Instrumental Activities of Daily Living scale)Baseline (0 week) and after intervention (8 weeks)Functional independence in older adults with disabilities will be assessed using the Instrumental Activities of Daily Living (IADL) scale. Scores range from 0 to 34 and will be converted to a standardized 0-100 scale for analysis. Higher scores indicate better ability to perform instrumental activities of daily living.
Intrinsic capacity (Title: Integrated Care for Older People)Baseline (0 week) and after intervention (8 weeks)Intrinsic capacity in older adults with disabilities will be assessed using the Integrated Care for Older People (ICOPE) framework. The assessment includes cognitive function, mobility, nutritional status, vision, hearing, and depressive symptoms. Higher levels of impairment indicate greater decline in intrinsic capacity.
Self-reported physical activity (Scale title: Chinese Version of the Physical Activity Scale for the Elderly)Baseline (0 week) and after intervention (8 weeks)Self-reported physical activity in older adults with disabilities will be assessed using the Chinese Version of the Physical Activity Scale for the Elderly (PASE-C). Scores are calculated by weighting different physical activities according to their frequency and duration of performance. Higher scores indicate higher levels of physical activity.

Countries

Taiwan

Contacts

CONTACTKai-Chia Cheng, PhD
kccheng@nhri.edu.tw+886-5-6204000
PRINCIPAL_INVESTIGATORChueh-Ho Lin, PhD

National Health Research Institutes, Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 22, 2026