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Alternative Carer Respite: A Study on Its Effectiveness and Potential Mechanism (VRDCFIn-home1)

The University of Hong Kong (HKU) logo

The University of Hong Kong (HKU)

Status

Enrolling

Conditions

Caregiver Burden

Treatments

Other: 48 hr Respite Service

Study type

Interventional

Funder types

Other

Identifiers

NCT07004842
EA230565

Details and patient eligibility

About

The primary objective of this study is to examine the effectiveness of alternative carer respite in meeting the unique needs of older adults without children or with limited contact with their children in Hong Kong. Caregivers are assessed before and after the intervention, and three months after the end of intervention on their physical health, mental well-being, social engagement, and overall satisfaction.

Full description

All participants will provide informed consent at the time of enrolment. Both caregivers and their care recipients will complete an assessment. Caregivers are screened for their physical health, mental well-being, social engagement, and overall satisfaction. Care recipients are screened using InterRAI for their physical functions.

Caregivers will receive a maximal of 48 hours of respite service within 6 month. Alternative caregivers will provide in-home elderly-sitting service so that the caregivers can have some private time for themselves.

At the end of the service period, 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 months after the completion of service.

Enrollment

30 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Either the CR or CG is aged ≥60
  • Reported having (a) no children; OR (b) no children in Hong Kong; OR (c) having children in Hong Kong but with limited contact (i.e., fewer than once per month in any forms)
  • Voluntary participation.

Exclusion criteria

  • Unable to communicate in neither Cantonese, English nor Mandarin

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Caregivers
Experimental group
Description:
Caregivers will receive 48 hours of respite service within 6 months
Treatment:
Other: 48 hr Respite Service

Trial contacts and locations

1

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Central trial contact

Vivian Weiqun Lou, PhD; Linda Dongling Wang, PhD

Data sourced from clinicaltrials.gov

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