The Effect of Music Therapy on Upper Extremity Functions and Quality Of Life in Individuals With Cerebral Palsy
NCT ID: NCT06209840
Last Updated: 2024-01-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
24 participants
INTERVENTIONAL
2023-03-01
2024-06-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Control Group
Classical physiotherapy program will be applied for gross motor functions and upper extremity functions.
Control Group
The session is 50 minutes long and consists of 20 minutes of classical physiotherapy for gross motor functions and 30 minutes of classical physiotherapy for the upper extremity. A total of 16 sessions will be applied 2 days a week for 8 weeks.
Study (Music) Group
In addition to the classical physiotherapy program for gross motor functions, will be applied in the Neuro-Creative Music Therapy (NCMT) program for upper extremity.
Study (Music) Group
The session is 50 minutes long and consists of 20 minutes of classical physiotherapy for gross motor functions and 30 minutes of music therapy for the upper extremity. A total of 16 sessions will be applied 2 days a week for 8 weeks.
Interventions
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Control Group
The session is 50 minutes long and consists of 20 minutes of classical physiotherapy for gross motor functions and 30 minutes of classical physiotherapy for the upper extremity. A total of 16 sessions will be applied 2 days a week for 8 weeks.
Study (Music) Group
The session is 50 minutes long and consists of 20 minutes of classical physiotherapy for gross motor functions and 30 minutes of music therapy for the upper extremity. A total of 16 sessions will be applied 2 days a week for 8 weeks.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* With upper extremity dysfunction
* MACS score between 2-4,
* According to MAS, spasticity severity ranges from (1+) to (3),
* Individuals diagnosed with hemiparetic Cerebral Palsy who are at a cognitive level that can follow simple instructions during applications and evaluations will be included.
Exclusion Criteria
* Having undergone upper extremity orthopedic surgery or Botulinum Toxin A (BTX-A) application in the last 6 months,
* Individuals currently receiving another rehabilitation program in addition to classical physiotherapy for upper extremity rehabilitation will be excluded from the study.
6 Years
21 Years
ALL
No
Sponsors
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Ankara Yildirim Beyazıt University
OTHER
Responsible Party
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Nezehat Özgül
Lecturer
Principal Investigators
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Sena ÇARIKCI, MSc
Role: PRINCIPAL_INVESTIGATOR
Ankara Yıldırım Beyazıt University Health Sciences Institute
Nezehat Özgül ÜNLÜER, PhD
Role: STUDY_CHAIR
Saglik Bilimleri Universitesi
Şükrü TORUN, MD
Role: STUDY_CHAIR
Anadolu University Health Sciences Institute
Locations
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Sena ÇARIKCI
Ankara, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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AYBU-NOUNLER-001
Identifier Type: -
Identifier Source: org_study_id
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