Actively Recruiting
BrainLive Connect: Volunteer Training Programme
Led by The University of Hong Kong · Updated on 2026-04-29
180
Participants Needed
1
Research Sites
90 weeks
Total Duration
On this page
Sponsors
T
The University of Hong Kong
Lead Sponsor
S
Simon K.Y.Lee Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this mixed method clinical trial is to evaluate whether BrainLive Coach training can enhance knowledge, skills, and wellbeing among young old volunteers. The main question it aims to answer are: • Do trained BrainLive Coaches demonstrate greater CST-related knowledge/skills, self-efficacy, and improved quality of life compared with volunteers receiving only educational materials? Researchers will compare the BrainLive Coach training group vs. general service group (young old volunteers) to see whether the intervention leads to enhanced dementia knowledge, sense of competence in dementia care, and approaches to dementia. Participants will be: 1. Adults aged 50 and over - volunteers (nRCT) * Participate in either 80-90 hours of BrainLive Coach training followed by volunteering in BrainLive Connect or receive educational materials on dementia and cognitive health. * Complete assessments at baseline (T0) and post intervention (T1) on dementia knowledge, competence in dementia care, self-efficacy, attitudes to dementia, quality of life, and social capital. 2. Qualitative study participants • Take part in individual interviews or focus groups, including trained volunteers, and NGO staff, to explore perceived impacts, mechanisms, implementation facilitators/barriers, and areas for improvement.
CONDITIONS
Official Title
BrainLive Connect: Volunteer Training Programme
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hong Kong residents
- Aged 50 and over
- Education level of Form 3 or above
- Fluent in Cantonese
- Able to read and write Chinese
You will not qualify if you...
- Unable to communicate and participate in interviews, training, or intervention due to hearing impairment, visual impairment, or other conditions
AI-Screening
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Trial Site Locations
Total: 1 location
1
The University of Hong Kong
Hong Kong, Hong Kong
Actively Recruiting
Research Team
J
JACKY CP CHOY, PhD
CONTACT
S
Shiyu LU, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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