Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
Healthy Volunteers
NCT07544875

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

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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