- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03778398
Music Therapy In Adolescents With Cerebral Palsy
The Effect Of Music Therapy On Upper Extremity Functions In Adolescents With Cerebral Palsy
Purpose of the study;
- To improve the upper extremity motor functions of patients with adolescent cerebral palsy,
- Prevent treatment interruptions as age progresses,
- Increase the hand functions of children with cerebral palsy and to increase their living standards.
Hand functions will be assessed with MACS (Manual Ability Classification System), hand dynamometer, box-block test, 9 hole peg test, pressing velocity measured with Cubase MIDI (musical instrument data interface) program. Patients will receive 2 days of 40 minutes per week, total 3 months of customized piano training. Each session will be started with finger warming exercises, then with the right hand, left handed and with both hands, a simple pentatonic array will be played. In the following lessons, notes will be marked with colors and simple songs will be taught. At the end of 3 months, the tests will be repeated.
Study Overview
Detailed Description
Cerebral palsy is the development, movement and posture disorder that causes the limitation of activity which is thought to be caused by non-progressive disorders in the fetal or infant brain. Intensive rehabilitation program begins in early childhood; However, adults with cerebral palsy are less likely to receive rehabilitative interventions. There is a great need for effective upper extremity rehabilitation studies that motivate the patient in CP (cerebral palsy) rehabilitation after childhood. Therapeutic Instrumental Music Performance (TIMP) is one of the three techniques of neurological music therapy techniques for motor rehabilitation. This technique uses instruments to strengthen functional motor patterns. There are very few studies on TIMP in individuals with cerebral palsy and these studies have not been performed on patients with adolescent cerebral palsy.
Purpose of the study;
- To improve the upper extremity motor functions of patients with adolescent cerebral palsy,
- Prevent treatment interruptions as age progresses,
- Increase the hand functions of children with cerebral palsy and to increase their living standards.
Inclusion Criteria:
- Being 11-18 years old
- To be diagnosed with cerebral palsy
- Not have been previously trained piano
- To have enough cognitive function to perform commands
- Accepted to participate in the study
Criteria for not being included in research:
- Having cognitive disorder
- Advanced visual impairment, visual field defect
- To be previously trained for piano
- Another disease preventing upper extremity movements
Hand functions will be assessed with MACS (Manual Ability Classification System), hand dynamometer, box-block test, 9 hole peg test, pressing velocity measured with Cubase MIDI (musical instrument data interface) program. Patients will receive 2 days of 40 minutes per week, total 3 months of customized piano training. Each session will be started with finger warming exercises, then with the right hand, left handed and with both hands, a simple pentatonic array will be played. In the following lessons, notes will be marked with colors and simple songs will be taught. At the end of 3 months, the tests will be repeated.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey, 34732
- Recruiting
- Istanbul Medeniyet University Faculty of Medicine, Physical Therapy and Rehabilitation Department
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Being 11-18 years old
- To be diagnosed with cerebral palsy
- Not have been previously trained piano
- To have enough cognitive function to perform commands
- Accepted to participate in the study
Exclusion Criteria:
- Having cognitive disorder
- Advanced visual impairment, visual field defect
- To be previously trained for piano
- Another disease preventing upper extremity movements
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Neurologic music therapy
Patients will receive 2 days of 40 minutes per week, total 3 months of customized piano training.
Each session will be started with finger warming exercises, then with the right hand, left handed and with both hands, a simple pentatonic array will be played.
In the following lessons, notes will be marked with colors and simple songs will be taught.
|
Customized piano training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improved hand function
Time Frame: 3 months
|
Improvement on MACS (Manual Ability Classification System)
|
3 months
|
|
Improved hand strength
Time Frame: 3 months
|
Improvement on hand dynamometer and pressing velocities measured by Cubase MIDI (musical instrument data interface) program
|
3 months
|
|
Improved fine motor skills
Time Frame: 3 months
|
Improvement on box-block test
|
3 months
|
|
Improved fine motor skills
Time Frame: 3 months
|
Improvement on 9 hole peg test
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improved hand coordination
Time Frame: 3 months
|
observational, development of the ability to play the piano with two hands
|
3 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IMU FTR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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