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Jockey Club Stand-by-U Caregivers Community Support Project: In-home Respite for Caregivers of Older Adults

Jockey Club Stand-by-U Caregivers Community Support Project

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06981117
Acronym
StandByU2
Enrollment
5166
Registered
2025-05-20
Start date
2024-04-01
Completion date
2027-10-31
Last updated
2025-05-20

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

Conditions

Caregiver Burnout, Caregiver Wellbeing

Keywords

caregiver, caregiving burden, caregiver wellbeing

Brief summary

The goal of this study is to investigate whether the in-home respite service model is effective in relieving caregiver's burden and improving their mental wellbeing. Caregivers are triaged into four levels of needs using a self-developed screening tool. Those screened as mild and moderate levels are admitted to the study, while those in low or high-needs levels are referred to other services. Caregivers admitted in this study will receive either 12 or 36 hours of in-home respite services as the intervention. Trained volunteers or substitute caregivers will visit their home to take care the older adults, providing several hours of free time for the caregivers. Assessments are conducted before and immediate after the intervention, and 3, 6, 12 months after the completion of intervention, to measure the changes in mental wellbeing of the caregivers. A control group with no respite service provided is recruited to compare the effects in the changes of mental wellbeing.

Detailed description

All participants will provide informed consent at the time of enrolment. Both caregivers and their care recipients will complete assessment before the respite service period. Care recipients are assessed for their self-dependent ability in daily activities and their physical health condition. Caregivers are screened for their overall needs level using a self-developed multidimensional screening tool. Those screened as High Needs level will be referred professional services. Those screened as Low will be recommended to join centre-based services. Caregivers who are in Mild or Moderate needs levels will be admitted to this project. They are also assessed using standard tests for measuring changes in mental health (using Depression Anxiety Stress Scales - Short Form (DASS-21)), caregiving burden (using Chinese Version of the Zarit Caregiver Burden Interview) and quality of life (using EQ-5D-5L). As the intervention, caregivers in Mild-needs level will receive 12 hours of in-home respite service, whereas those in Moderate-level will receive 36 hours of service. Volunteer or substitute caregivers will provide in-home elderly-sitting service so that the caregivers can have some private time for themselves. At the end of the intervention, caregivers and care recipients will complete the assessment again to measure the changes of their physical and mental health. All participants will be contacted again for follow-up assessment 3, 6 and 12 months after the completion of intervention. A control group with no respite service provided is recruited to compare the effects in the changes of mental wellbeing. They are contacted 3, 6 and 12 months after baseline measurement.

Interventions

OTHER12 hr Respite Service

12 hours of respite service within 3 months will be provided by volunteers. Volunteers will provide elderly-sitting service (accompany the care recipient) during the service session, and provide cognitive training or physical training to the care recipient if situation allows.

OTHER36 hr Respite Service

36 hours of respite service within 3 months will be provided by substitute caregivers. Substitute caregivers will provide elderly-sitting service (accompany the care recipient) during the service session, and provide cognitive training or physical training to the care recipient if situation allows.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

Caregivers and Control group Inclusion Criteria: * aged 18 or above * provide care to at least one homebound older adult (aged 60 or above) * provide no less than 6 hours of caregiving per week * able to communicate in either Cantonese, Mandarin or English

Exclusion criteria

* Care recipient is receiving long-term care service

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in score in caregiving needs measured by Multidimensional screening tool after the interventionBaseline and Immediate after interventionThe Multidimensional screening tool is a self-developed tool that measures different aspects of caregiving needs over the past 1 week period. It is a 22-item scale, with 8 items that determines the overall needs level and the others for four aspects of needs: physical health, mental health, social support and care needs. Possible score is from 8 to 32 with lower score indicates lower caregivers' needs. Change in score = Immediate after intervention - baseline
Change from baseline in score in mental wellbeing measured by DASS-21 scale after interventionBaseline and Immediate after interventionThe DASS-21 comprises 21 items that assess symptoms of depression, anxiety, and stress over the past week. Each item is rated on a 4-point Likert scale, with higher scores indicating greater symptom severity. The total scores for each subscale (Depression, Anxiety, Stress) are calculated by summing the relevant item scores. Possible score for each subscale ranged from 0 to 42, with 0 indicates best outcome and 42 the worst outcome. Reductions in DASS-21 scores indicate improvements in symptoms of depression, anxiety, and stress following the intervention. Change in score = Immediate after intervention- baseline
Change in score from baseline in caregiving burden measured by CZBI after interventionBaseline and Immediate after interventionThe Chinese version of Zarit Caregiver Burden Inventory (CZBI) is a widely used tool designed to assess caregiver burden and distress experienced by individuals caring for a loved one with a chronic illness or disability. It comprises of 12 items, and each item is rated on a 5-point Likert scale. Possible score ranged from 0 to 48, with higher scores indicating greater levels of caregiver burden. Change in score= Immediate after intervention - baseline
Change in score from baseline in quality of life measured by EQ-5D-5L after interventionBaseline and Immediate after interventionThe EQ-5D-5L is a standardized instrument used to assess health-related quality of life across five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The responses are converted into a single index value representing overall health status using Hong Kong's normative value. The primary outcome measure in this study is the change in EQ-5D-5L index scores from baseline to post-intervention/follow-up assessments. 1 equals to perfect health and more negative numbers indicates worse health. Change in health index = Immediate after intervention - baseline
Retention of changes of Primary outcome 1 to 4 after the end of interventionBaseline, immediate after service, 3, 6 and 12 months after the interventionCaregivers will complete the primary outcome measurements (1 to 4) again 3, 6 and 12 months after the end of the intervention. They will not receive any in-home respite service from the project in between the measurement periods. Changes in score of each scale in Primary Outcome 1 to 4 will be measured. Participants with improved/sustained score indicates better retention.

Other

MeasureTime frameDescription
Respite service details in each session, including the duration and contentAfter each respite sessionVolunteer and Substitute Caregivers will provide a service record after each respite session, detailing the activities in each session and any potential problems observed. Measurements include the time of each respite session and the type of activities the caregivers and care recipient do in each session.

Countries

Hong Kong

Contacts

Primary ContactVivian Weiqun WQ Lou
wlou@hku.hk852-39174835

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026