- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06324227
Effects of Multimodal Music Intervention on Mild Cognitive Impairment Elderly
March 19, 2024 updated by: National Yang Ming University
Effects of Multimodal Music Intervention on Cognitive Function, Physical Fitness and Psychology of the Community Dwelling Elderly With Mild Cognitive Impairment
The goal of this clinical trial is to learn about whether music therapy can ameliorate cognitive function, physical fitness and psychology in mild cognitive impairment and mild dementia population. The main questions it aims to answer are:
- To build a model of multimodal music therapy.
- To discuss the effect of twelve-week multimodal music therapy in ameliorating community-based elders with MCI and mild dementia. Main outcome variables: cognitive function (Montreal Cognitive Assessment Scale, trail making test, Saint Louis University Mental Status Examination). Secondary outcome variables: physical fitness (muscle strength, muscular endurance, flexibility, balance ability), depression.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The prevalence of the elderly with mild cognitive impairment accounts for one-fifth of the elderly population in Taiwan, and there is no medication that can effectively treat the disease.
According to the literature review, there are many factors that cognitive impairment would influence.
Many chronic diseases can induce cognitive decline, and depression is also related to cognitive function, including memory loss and cognitive decline.
Mild cognitive impairment or dementia are also related to disability.
Therefore, we choose the music, mood and movement(MMM) theory to connect psychology, cognitive function and physical fitness.
The purpose of the research is to establish a model of the multimodal music therapy model and explore the effect of the multimodal music therapy on improving the mild cognitive impairment and mild dementia in the community.
The senior with mild cognitive impairment and mild dementia are divided into an experimental group and a control group through randomization consisted of total 49 people based on different day care centers or community-based dementia care centers.
It will take 12 weeks for the intervention.
The experimental group received multimodal music intervention twice a week, each time with a duration of 70 minutes.
The design method partly refers to the methods designed by Shimizu, including three musical instruments for the music therapy and physical activity, and the control group does not have any intervention.
The experimental group and the control group have two weeks of pre-test and post-test, and the information sheet of demography, Montreal Cognitive Assessment, Saint Louis University Mental Status Exam, Trail Making Test, muscle strength and endurance, flexibility and dynamic balance ability, Geriatric Depression Scale would be collected before and after the 12-week intervention.
The research data is analyzed with Statistical Product and Service Solutions(SPSS).
We expect cognitive function, physical fitness and psychology can be improved through multimodal music therapy.
This study is also the first time using music, mood and movement theory and applied to multimodal music therapy in Taiwan.
If the research results are beneficial, this theory would become a beneficial choice for the elderly with cognitive decline.
Study Type
Interventional
Enrollment (Estimated)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tzu Ting Huang, Professor
- Phone Number: 65323 02-28267016
- Email: thuang@nycu.edu.tw
Study Locations
-
-
-
Taipei, Taiwan
- Recruiting
- NationalYangMingU
-
Contact:
- Wei Zu Lo
- Phone Number: 66378 02-2823-9753
- Email: weitzu@nycu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- diagnosed with mild dementia
- not diagnosed with dementia, but are suspected cases, including chief complaint or clinical dementia rating scale 0.5.
- more than 65 years old
Exclusion Criteria:
- having severe hearing impairment, or can not talk with Chinese or Taiwanese
- having exercise contraindication
- diagnosed with other psychiatric disorders
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: multimodal music therapy group
using twice a week, 12 weeks music intervention with singing and physical movement with rhythm
|
music therapy
|
|
Experimental: no intervention group
no intervention
|
no intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Montreal Cognitive Assessment
Time Frame: about 15 minutes
|
The Montreal Cognitive Assessment scale(MoCA) has seven major cognitive functions, including short-term memory, visuospatial, executive function, language ability, attention, abstract reasoning, and orientation.
The minimum score is 0 and the highest score is 30.
There are total score of 30 points.
Considering the literacy, the lower points means the more severe the cognitive function is.
|
about 15 minutes
|
|
Saint Louis University Mental Status
Time Frame: about 15 minutes
|
The Saint Louis University Mental Status(SLUMS) scale includes five major cognitive function: orientation, memory, attention, executive function and language ability.
There are 11 questions with a total score of 30 points.
The minimum score is 0 and the highest score is 30.
There are total score of 30 points.
The lower points means the more severe the cognitive function is.
|
about 15 minutes
|
|
Trail Making Test
Time Frame: about 10 minutes
|
The test is designed to examine the attention and can be divided into two parts.
There are number 1-25 in circles that appear randomly on the paper.
There are Chinese Zodiac and twelve numbers in Trail Making Test-B.
|
about 10 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
30s chair stand
Time Frame: 30 seconds
|
stand up and sit down in 30 seconds to calculate how many times
|
30 seconds
|
|
back scratch test
Time Frame: 15 seconds
|
two hands need to reach in your back, one hand on upper and another on lower position
|
15 seconds
|
|
sit and reach test
Time Frame: 15 seconds
|
sit on the floor with legs stretched out straight.
Then reach forward as far as possible with hands
|
15 seconds
|
|
8-foot up-and-go test
Time Frame: 15 seconds
|
calculate the time the participant walk a round trip in a line with 2.44 meters
|
15 seconds
|
|
handgrip
Time Frame: 15 seconds
|
participants hold handgrip dynamometer in each hand and squeeze the device as hard as they could to calculate how many kilograms
|
15 seconds
|
|
Geriatric Depression Scale 15 items
Time Frame: 10 minutes
|
This 15-question assessment scale is mainly used to detect the tendency of depression in the elderly.
Answer "yes" or "no" by reading the questions and comparing their own psychological status.
The total score is 0-15.
Score 0-4 indicates no tendency to be depressed, 5-10 indicates a tendency to be depressed, and 10-15 indicates a tendency to be severely depressed.
The higher the score, the higher the tendency of depression.
|
10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Tzu Ting Huang, Professor, National Yang Ming University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 17, 2023
Primary Completion (Estimated)
March 26, 2024
Study Completion (Estimated)
May 26, 2024
Study Registration Dates
First Submitted
February 19, 2024
First Submitted That Met QC Criteria
March 19, 2024
First Posted (Actual)
March 21, 2024
Study Record Updates
Last Update Posted (Actual)
March 21, 2024
Last Update Submitted That Met QC Criteria
March 19, 2024
Last Verified
November 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 311203003
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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