- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04221386
Melodic Intonation Therapy for Tone Language Speakers
April 8, 2020 updated by: The Hong Kong Polytechnic University
One of the traditional therapies for restoring the ability of speech in aphasic patients is Melodic Intonation Therapy (MIT), in which everyday phrases are taught in a singing-like manner.
The suggested mechanism for speech recovery is that because of the sharing of brain resources for language and music, the regions normally reserved for singing can be trained to help compensate the speech functions originally subserved by the damaged regions.
However, this therapy has primarily been applied to speakers of non-tone languages, in which prosodic features carry a more important role than pitch features in conveying meanings.
It remains unknown whether MIT will be equally applicable for speakers of tone languages, in which pitch features likely play a more important role.
Another uncertainty concerns whether the efficacy of MIT can be extended to patients with expressive speech impairment due to dementia.
This pilot study aims to find out the efficacy of MIT for speech-impaired dementia patients in different verbal tasks.
The results of this study will provide preliminary empirical evidence to establish the utility of MIT for Cantonese speakers in Hong Kong.
Study Overview
Status
Suspended
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
40
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 Locations
-
-
-
Hong Kong, Hong Kong
- Elderly homes
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-
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
46 years to 96 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Early to moderate stage dementia patient
- Normal hearing (hearing aid accepted)
- Non-fluent speech (max. score of fluency in Cantonese Aphasia Battery spontaneous speech subtest = 6/10)
Exclusion Criteria:
- Non-native Cantonese speaker
- Illiterate
- Aphasic patients
- Subjects who receive other speech therapy during study
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MIT group
Subjects will receive the developed Melodic Intonation Therapy.
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Subjects will receive at least 6 MIT sessions in group of 3-5 subjects.
In the sessions, experimenter will sing songs with the subjects.
Songs used in the intervention are familiar to elderly and are rewritten and embedded with everyday phrases and vocabularies.
The whole intervention will span 3-4 weeks.
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No Intervention: Control group
Subjects will not receive any intervention.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Aphasia Quotient (AQ) in Cantonese Aphasia Battery
Time Frame: within a week after procedure
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Two subtests of the Cantonese Aphasia Battery (auditory comprehension & spontaneous speech) will be executed.
Higher AQ means better performance in the respective areas.
The minimum of AQ in each subtest is 0, and the maximum is 20.
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within a week after procedure
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in latency and accuracy in picture naming task
Time Frame: within a week after procedure
|
In the computerized picture naming task, subjects are asked to name the objects they see in 52 pictures, within 5000 ms per picture.
Visual stimuli of the task are black and white line-drawings.
Responses are all recorded for analysis.
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within a week after procedure
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Change in performance of semantic fluency task
Time Frame: within a week after procedure
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In the computerized semantic fluency task, subjects are given 5 categories (e.g.
animals) and asked to name as many members of the categories (e.g.
cat, dog) as possible.
For each category, they have one minute to respond.
All the responses are recorded for analysis.
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within a week after procedure
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: William Shi Yuan Wang, Ph.D., The Hong Kong Polytechnic University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Albert ML, Sparks RW, Helm NA. Melodic intonation therapy for aphasia. Arch Neurol. 1973 Aug;29(2):130-1. doi: 10.1001/archneur.1973.00490260074018. No abstract available.
- Sparks R, Helm N, Albert M. Aphasia rehabilitation resulting from melodic intonation therapy. Cortex. 1974 Dec;10(4):303-16. doi: 10.1016/s0010-9452(74)80024-9. No abstract available.
- Sarkamo T, Sihvonen AJ. Golden oldies and silver brains: Deficits, preservation, learning, and rehabilitation effects of music in ageing-related neurological disorders. Cortex. 2018 Dec;109:104-123. doi: 10.1016/j.cortex.2018.08.034. Epub 2018 Sep 19.
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 (Anticipated)
August 1, 2020
Primary Completion (Anticipated)
December 31, 2020
Study Completion (Anticipated)
February 28, 2021
Study Registration Dates
First Submitted
January 3, 2020
First Submitted That Met QC Criteria
January 6, 2020
First Posted (Actual)
January 9, 2020
Study Record Updates
Last Update Posted (Actual)
April 10, 2020
Last Update Submitted That Met QC Criteria
April 8, 2020
Last Verified
December 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IZZKJ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
All the data collected in screening, pre- and post-assessment will not be shared with other researchers.
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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