Spastic Diplegia Cerebral Palsy Clinical Trial
Official title:
Comparison of Massage Therapy and Tissue Flossing Technique in Children With Diplegic Cerebral Palsy
The purpose of the study is to compare massage therapy with tissue flossing technique in children with diplegic cerebral palsy. A randomized control trial would be conducted at helping hand for relief and development Quetta. The sample size is 56 calculated through G power. The participants would be divided into two interventional groups each having 28 participants. The study duration would be six weeks. Sampling technique applied would be convenient sampling for recruitment and group randomization via using envelop method. Tools used in this study are Goniometer, muscle length test and Functional Mobility scale. Data would be collected before and after 6 weeks of the application of interventions. Data analyzed through SPSS version 23.
Status | Recruiting |
Enrollment | 56 |
Est. completion date | January 28, 2024 |
Est. primary completion date | January 5, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 12 Years to 15 Years |
Eligibility | Inclusion Criteria: Participants falling in this category would be recruited into the study. - Both genders (male and female). - Age between 12 - 15 years. - Diagnosed patients of spastic diplegic cerebral palsy. - Muscle tone between (1 and 1+) according to modified Ashworth scale. - Gross motor function classification system level will be from I to IV. - Children who has communication skills (according to communication function classification system, level I - III). Exclusion Criteria: Participants falling in this category would be excluded from the study. - Previous Fracture/Trauma of lower limb less than six month prior to the study. - Soft tissue injury of lower limb less than six month prior to the study. - History of any surgical intervention for the management of spasticity or any orthopedic surgery of lower limb. - Any therapeutic intervention for the management of spasticity i-e (botulinum injections, ITB and drugs) less than six month prior to the study. - Children with multiple disabilities. - Seizure. - Latex allergy. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Helping Hand For Relief and Development Quetta | Quetta | Balochistan |
Lead Sponsor | Collaborator |
---|---|
Riphah International University |
Pakistan,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Goniometery | It is an instrument that measures the available range of motion at a joint. It will used to determine range of motion of hip, knee and ankle joint (16). | Base Line measurement before start of treatment and post 6th Week | |
Primary | Muscle length test | Muscle length test of rectus femoris, hip adductors, hamstring, gastrocnemius and soleus will be performed to determined muscular flexibility (17). | Base Line measurement before start of treatment and post 6th Week | |
Primary | Functional mobility scale | It is an instrument that measures the available range of motion at a joint. Functional mobility scale will be used to determined mobility (18). | Base Line measurement before start of treatment and post 6th Week |
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