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Smart Taiko-Drum Playing for Older Adults With Cognitive Frailty

T

The Hong Kong Polytechnic University

Status

Enrolling

Conditions

Cognitive Impairment
Frailty

Treatments

Behavioral: Smart Taiko Drumming

Study type

Interventional

Funder types

Other

Identifiers

NCT06115889
P0046219

Details and patient eligibility

About

The objective of this randomised controlled feasibility trial is to evaluate the feasibility of the Smart Taiko Drum-playing intervention embedding the cognitive-motor dual-task training concept for older adults with cognitive frailty, and identify the preliminary efficacy of the intervention on cognitive and physical functions and frailty status.

Full description

  1. Study design:

    • 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

Enrollment

60 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • with cognitive frailty
  • 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

  • with a significant sensory or motor impairment that would preclude participation in the intervention
  • 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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Smart Taiko Drumming Group
Experimental group
Description:
Smart Taiko Drumming
Treatment:
Behavioral: Smart Taiko Drumming
Usual Care Waitlist Control Group
No Intervention group
Description:
Usual care

Trial contacts and locations

1

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Central trial contact

Daphne Sze Ki Cheung, PhD; Daphne Sze Ki Cheung, PhD

Data sourced from clinicaltrials.gov

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