Actively Recruiting

Phase Not Applicable
Age: 55Years +
All Genders
ID07105800

A Pilot Study of Dance Intervention for Enhancing Executive Function and Physical Performance in Cognitively Impaired Older Adults

Led by Taipei Medical University Shuang Ho Hospital · Updated on 2026-04-28

50

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the effects of a music-based dance program on executive function and physical performance in middle-aged and older adults with cognitive impairment. It focuses on mild cognitive impairment, a condition that affects memory, judgment, and motor skills, often reducing independence and quality of life. Dance, combining music, rhythmic movement, and cognitive-motor coordination, offers dual-task training that may improve both cognitive and motor functions simultaneously through social interaction and partner guidance. Participants are assigned to either the music-based dance intervention group or a control group. The intervention group takes part in a nine-week, twice-weekly group dance program with 40-minute sessions featuring rhythmic movement, fixed choreography, and mutual physical guidance to stimulate memory, attention, balance, and lower limb mobility. The control group follows a nine-week, twice-weekly lower limb exercise program delivered by non-musical instructional videos focusing on strength and balance training. Participants are assessed at three points: before the intervention, mid-intervention at week 5, and one week after completion at week 10. Evaluations include cognitive tests like the Montreal Cognitive Assessment and Stroop Color and Word Test, as well as physical performance tests such as the Four-Square Step Test, Timed Up and Go - Cognitive, and Functional Reach Test. Feedback is also collected after the program. Data analysis examines changes within and between groups to understand the intervention's feasibility and preliminary effects.

CONDITIONS

Brief Title

Dance Intervention to Improve Executive Function and Physical Performance in Older Adults With Cognitive Impairment

Who Can Participate

Age: 55Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjective Cognitive Decline with a score of 5 or higher on the SCD-Q9 questionnaire, or Mild Behavioral Impairment with a score of 7 or higher on the MBI-Checklist, lasting more than three months
  • Ability to follow instructions
  • Ability to stand unsupported or with assistive devices for at least 10 minutes
  • Ability to walk at least 10 meters, unsupported or with assistive devices
Not Eligible

You will not qualify if you...

  • Age below 55 years
  • Severe visual or hearing impairment
  • Montreal Cognitive Assessment score below 16
  • Emotional or anxiety symptoms caused by psychiatric medications that significantly impair motor task performance

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 9 weeks

Participants take part in a structured, nine-week program. The intervention group attends twice-weekly group-based music and dance sessions focused on cognitive and physical skills, while the control group follows a twice-weekly lower limb exercise program via instructional videos.

Twice-weekly visits for 9 weeks

Outpatient Treatment

Duration - 10 weeks

Assessments are conducted at three time points: before the program starts, at the midpoint (week 5), and after the program ends (week 10) to evaluate cognitive and physical performance improvements.

3 assessment visits (pre-intervention, mid-intervention, post-intervention)

Trial Site Locations

Total: 1 location

1

Taipei Medical University Shuang Ho Hospital

New Taipei City, Taiwan, Taiwan, 235

Actively Recruiting

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Research Team

F

Fen-Ling Kuo, Master

C

ChiehYu Pan, Master

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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