Clinical Trial

BrainLive Connect: Non-professional Delivered CST for People Living With Dementia

Recruiting
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Summary
The goal of this mixed method study is to evaluate whether the volunteer-led Cognitive Stimulation Therapy (CST) under the BrainLive Connect programme is effective for improving cognitive function and quality of life of people living with dementia (PLwD). The main question it aims to answer are: • Do PLwD receiving the BrainLive Connect service show better cognitive function and quality of life than those receiving usual care? Researchers will compare BrainLive Connect service to usual care to see whether the intervention leads to better outcomes. Participants will: * Receive either 7 weeks of BrainLive Connect sessions delivered by trained volunteers or continue receiving usual care. * Be assessed at baseline (T0), post-intervention (7 weeks; T1), and 1 month follow up (11 weeks; T2). * Take part in semi-strucutred interviews post-intervention to provide feedback on implementation and areas for improvement.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-08.
Trial Details
NCT Number NCT07531589
Lead Sponsor The University of Hong Kong
Collaborators: Simon K.Y.Lee Foundation, Yang Memorial Methodist Social Service, Christian Family Service Centre, Hong Kong Young Women's Christian Association
Conditions Dementia
Enrollment 520 participants
Start Date 2026-03-31
Primary Completion 2027-11-10 (estimated)
Study Completion 2027-11-10 (estimated)
Updated on ClinicalTrials.gov 2026-04-21