Assistive Device Rental/Purchase, LTC Service Use, and Caregiver Burden in Taiwan
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorNational Health Research Institutes, Taiwan
About this trial
The goal of this observational study is to examine the associations between assistive device approval and acquisition modality (rental or purchase), long-term care service utilization, and family caregiver burden among individuals receiving long-term care services in Taiwan. The study will use de-identified nationwide long-term care administrative data from 2021 to 2022.
The main questions it aims to answer are:
1. What individual, disability-related, socioeconomic, residential, and caregiving factors are associated with assistive device approval, the number and type of approved devices, and rental or purchase modality? 2. Are assistive device approval and utilization patterns associated with the use of formal long-term care services and with family caregiver burden?
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Individuals with a valid long-term care case record (CA100) in Taiwan's long-term care database between 2021 and 2022.
Individuals with at least one valid assessment or care plan record (CA110) that can be linked to the corresponding CA100 record.
Availability of interpretable key study variables, including individual and assessment/care plan identifiers, care plan status, and Case-Mix System (CMS) level or other core disability-related information.
For analyses of assistive device utilization, the presence or absence of an assistive device record (QD113) and its approval status must be identifiable.
Disqualifiers
Records with missing key linkage variables that prevent establishment of relationships among individuals, care plans, assistive device records, or service utilization records.
Records identified as invalid, cancelled, test records, or records whose validity cannot be determined.
Records in which primary study variables cannot be interpreted.
Records with clearly implausible values for variables such as individual age, caregiver age, CMS level, number of assistive devices, or service utilization that cannot be corrected according to prespecified data-cleaning rules.
Trial population
The study population will consist of individuals represented in Taiwan's nationwide long-term care administrative databases from 2021 to 2022. Eligible individuals must have a valid long-term care case record (CA100) and at least one valid linked assessment or care plan record (CA110). De-identified records will be used to examine assistive device approval and acquisition patterns, long-term care service utilization, and family caregiver-related characteristics and burden. No participants will be directly recruited or contacted.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Not listed
Trial groups
161,771 Participants
are grouped into 2 trial groupsGroup A: Assistive device approved
Group B: No assistive device approved
Trial outcomes
Primary outcomes
1
Assistive Device Approval Status
Whether an individual had an approved assistive device record, determined using the approval status recorded in the Assistive Technology File (QD113). Associations with disability severity, sociodemographic characteristics, residential characteristics, and caregiving conditions will be examined.
Time frame
During the 2021-2022 observation period2
Formal Long-Term Care Service Utilization
Utilization of formal long-term care services, including total service utilization and category-specific utilization of care services, professional services, transportation, respite care, meal services, and other long-term care services. Associations with assistive device approval, number of devices, acquisition modality, and device category will be examined.
Time frame
During the 2021-2022 observation period3
Family Caregiver Burden
Family caregiver burden will be assessed using available administrative-record indicators, including sleep disturbance, physical burden, competing caregiving demands, distress related to care-recipient behaviors, and inability to cope with caregiving stress. A cumulative caregiver burden indicator will also be derived from the number of burden items endorsed.
Time frame
During the 2021-2022 observation periodSecondary outcomes
1
Assistive Device Acquisition Modality
Acquisition modality of approved assistive devices, categorized as rental or purchase according to the Assistive Technology File (QD113) administrative record. Factors associated with rental versus purchase will be examined.
Time frame
During the 2021-2022 observation period2
Number and Category of Approved Assistive Devices
Number of approved assistive devices and device categories, such as mobility, transfer, bathing and toileting, home-care beds and bedside equipment, safety or monitoring devices, and communication or cognitive support devices.
Time frame
During the 2021-2022 observation periodSponsors and contacts
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Source ClinicalTrials.gov
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