This study is a feasibility randomized controlled trial (RCT) for an evidence-based intervention for people with moderate to severe dementia in Hong Kong. The psychosocial intervention is adapted from Cognitive Stimulation Therapy (CST), translated and adapted for the Hong Kong Chinese population, and developed within the Medical Research Council (MRC) framework.
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Recruitment (feasibility of ACST-HK)
Timeframe: Descriptive data will be collected during the study and analysed post-intervention; through study completion, 2 years
Retention rate (feasibility of ACST-HK)
Timeframe: Descriptive data will be collected during the study and analysed post-intervention; at 8-week follow-up
Negative of adverse events (acceptability of ACST-HK)
Timeframe: Descriptive data will be collected during the study and analysed post-intervention; through study completion, 2 years
Intervention fidelity (acceptability of ACST-HK)
Timeframe: Descriptive data will be collected during the study and analysed post-intervention; through study completion, 2 years
Intervention fidelity (acceptability of ACST-HK)
Timeframe: Descriptive data will be collected during the study and analysed post-intervention; through study completion, 2 years