Comparison of Task-oriented Activity Based Neurodevelopmental Principles and Gross Motor Task Training.
NCT ID: NCT05981287
Last Updated: 2023-08-08
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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COMPLETED
NA
20 participants
INTERVENTIONAL
2022-09-15
2023-04-05
Brief Summary
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Detailed Description
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This will be a Randomized Clinical Trial in which participants of age 5 - 12 years with cerebral palsy will be assigned randomly for the study. Population will be taken from Physical Therapy Department of Agile Rehabilitation Complex, Bahawalpur. After taking consent, demographics including age, gender and birth history etc. will be recorded. Questionnaires will be distributed among parents and their responses will be collected. Questionnaires for trunk impairment scale, postural assessment scale, pediatric balance scale and GMFM-88 will be used as tools of assessment. The collected data will be analyzed in Statistical Package for the Social Sciences (SPSS) 27.0.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Task-oriented activities based on NDT (TOA-NDT) principle and Conventional Physical Therapy
The experimental group undergo conventional physical therapy and additional task-oriented activities based on NDT (TOT-NDT) principle 10 - 36 sessions in 5-8 weeks, 2 to 6 days per sessions.
Task-oriented activities based on NDT (TOA-NDT) principle and Conventional Physical Therapy
This will be a randomized clinical trial. patients are divided into two groups. one of them will undergo task-oriented activities along with conventional physical therapy treatment, while the other will undergo gross motor task training along with conventional physical therapy treatment. Purpose is to determine that which of them has greater benefit in improving balance trunk control and functional mobility in children with cerebral palsy.
Gross motor task training and Conventional physical therapy (CPT)
This group will receive conventional physical therapy and additional gross motor task training 10-36 sessions in 5-8 weeks, 2 to 6 days per sessions.
Gross motor task training and Conventional physical therapy (CPT)
This will be a randomized clinical trial. patients are divided into two groups. one of them will undergo task-oriented activities along with conventional physical therapy treatment, while the other will undergo gross motor task training along with conventional physical therapy treatment. Purpose is to determine that which of them has greater benefit in improving balance trunk control and functional mobility in children with cerebral palsy.
Interventions
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Task-oriented activities based on NDT (TOA-NDT) principle and Conventional Physical Therapy
This will be a randomized clinical trial. patients are divided into two groups. one of them will undergo task-oriented activities along with conventional physical therapy treatment, while the other will undergo gross motor task training along with conventional physical therapy treatment. Purpose is to determine that which of them has greater benefit in improving balance trunk control and functional mobility in children with cerebral palsy.
Gross motor task training and Conventional physical therapy (CPT)
This will be a randomized clinical trial. patients are divided into two groups. one of them will undergo task-oriented activities along with conventional physical therapy treatment, while the other will undergo gross motor task training along with conventional physical therapy treatment. Purpose is to determine that which of them has greater benefit in improving balance trunk control and functional mobility in children with cerebral palsy.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Both boys and girls
* Age 5 - 12 years old
* Able to follow verbal commands
* Having level I or II of GMFCS
Exclusion Criteria
* On antiepileptic and anti-spastic medications
* Having visual or intellectual impairments
* Having hearing deficit
* With any cardiac anomalies affecting exercise tolerance
* Less than 6-month post-orthopedic surgery or post-botulinum toxin injections
5 Years
12 Years
ALL
No
Sponsors
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Riphah International University
OTHER
Responsible Party
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Principal Investigators
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Arnab Altaf, Mphill
Role: PRINCIPAL_INVESTIGATOR
Riphah International University
Locations
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Aamna Hassan
Bahawalpur, Punjab Province, Pakistan
Countries
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Other Identifiers
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REC/RCR & AHS/22/0720
Identifier Type: -
Identifier Source: org_study_id
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