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.
Age range
60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change from baseline in score in caregiving needs on the Carer Needs Screening Tool (CNST-11) after the intervention
Timeframe: Baseline and Immediate after intervention
Change from baseline in score in depression symptoms on PHQ-9 after the intervention
Timeframe: Baseline and Immediate after intervention
Change from baseline in score in anxiety symptoms on GAD-7 after the intervention
Timeframe: Baseline and Immediate after intervention
Change in score from baseline in quality of life measured by EQ-5D-5L after intervention
Timeframe: Baseline and Immediate after intervention
Changes in score from baseline in perception of caregiving measured by Positive Aspect of Caregiving scale after intervention
Timeframe: Baseline and Immediate after intervention