Smart Taiko-Drum Playing for Older Adults With Cognitive Frailty
NCT ID: NCT06115889
Last Updated: 2024-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2024-02-01
2025-06-30
Brief Summary
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Detailed Description
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\- Randomized Control Trial
2. Participants:
\- Community-dwelling older adults with cognitive frailty
3. Setting:
\- Community centres for seniors
4. Intervention
* Playing Smart Taiko three times/weeks x 16 weeks for 30 - 45 minutes each session
* A Smart Taiko Drumming system has been developed for older adults to play the drumming game with their preferred music genres.
5. Waitlist-control group
\- Will receive usual care
6. Health outcomes that will be assessed three times at baseline, during (8th week) and immediate post-intervention (16th week)
* cognitive functions
* physical functions
* mental health
* physical frailty status
* body composition
7. Feasibility evaluation
* recruitment
* retention
* satisfactory survey
* compliance with the survey
* safety
* focus group intervention with participants
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Smart Taiko Drumming Group
Smart Taiko Drumming
Smart Taiko Drumming
Participants will play drumming with the developed Smart Taiko Drumming System for 30-45 minutes three times per week for 16 weeks, in addition to usual care.
Usual Care Waitlist Control Group
Usual care
No interventions assigned to this group
Interventions
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Smart Taiko Drumming
Participants will play drumming with the developed Smart Taiko Drumming System for 30-45 minutes three times per week for 16 weeks, in addition to usual care.
Eligibility Criteria
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Inclusion Criteria
* without a diagnosis of a neurological or psychiatric condition that could affect cognitive function
* live independently or with partial assistance
* with pre-frailty
Exclusion Criteria
* are unable to understand or follow instructions due to language or hearing impairment
* have already been in another cognitive or physical intervention programme within the past three months
* are taking medications that could significantly affect cognitive or physical functions
* with any medical condition or treatment that would contraindicate participation in the study.
60 Years
ALL
No
Sponsors
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The Hong Kong Polytechnic University
OTHER
Responsible Party
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Principal Investigators
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Daphne Sze Ki Cheung, PhD
Role: PRINCIPAL_INVESTIGATOR
The Hong Kong Polytechnic University
Locations
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School of Nursing, The Hong Kong Polytechnic University
Hong Kong, , Hong Kong
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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P0046219
Identifier Type: -
Identifier Source: org_study_id
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