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Study identifier: NCT06648707 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Dual-task Training to Prevent Cognitive Decline in Community-dwelling Older Adults: A Pilot Pragmatic RCT

Condition: Community-dwelling Seniors  ·  Sponsor: The University of Hong Kong

PhaseNA
Planned participants93
Who can joinAll sexes, 65 Years to no upper limit
Healthy volunteersYes

About this study

Objectives: This study aims to explore the feasibility and acceptance of group-based dual-task training for prevention of cognitive decline in a pragmatic setting for community-dwelling older adults. The primary objective is to assess recruitment rate, attendance rate, retention rate and satisfaction rate of participants. Study design and participants: This is a pilot pragmatic RCT with waitlist control. First, a co-design approach will be adopted to develop the intervention with the older adults. Then, about six participating community centres will nominate staff or volunteer to receive the training in order to lead the intervention. Informed consent will be sought from the participants and baseline assessment will be conducted. The participants will be randomly allocated to the intervention and control groups in 1:1 ratio using block randomisation with varying block size. At the end of the study, one representative of each participating centre will be invited to provide qualitative feedback. Measurements: The primary outcomes are the feasibility outcomes, namely the recruitment rate, attendance rate, the retention rate, and satisfaction rate of participants. Secondary outcomes include completion rate of the interventionist, time to recruit target sample size, factors influencing older adults' decision to participate and staff of the community centre to organise the activity, subjective memory complaints, working memory, executive function, and cognitive status of part…

This description comes directly from the study's public registry record.

Talk to the study team

Pui Hing Chau, PhD  ·  3917 6626  ·  phpchau@hku.hk

Always discuss trial participation with your own doctor first.

Locations (1)

Community centreHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT06648707