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
40 participants
INTERVENTIONAL
2021-01-20
2021-04-30
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
SINGLE
Study Groups
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STUDY GROUP
they received progressive resistive functional strength training from plantigrade foot position conducted for one hour, 3 days/week. The therapist will replace the conventional physical therapy with the progressive resistive functional strength training, when this is consistent with the objectives of the strength training.
functional training exercises
progressive resistive functional strength training from plantigrade foot position conducted for one hour, 3 days/week. The therapist will replace the conventional physical therapy with the progressive resistive functional strength training, when this is consistent with the objectives of the strength training.
control group
received a designed physical therapy program
No interventions assigned to this group
Interventions
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functional training exercises
progressive resistive functional strength training from plantigrade foot position conducted for one hour, 3 days/week. The therapist will replace the conventional physical therapy with the progressive resistive functional strength training, when this is consistent with the objectives of the strength training.
Eligibility Criteria
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Inclusion Criteria
2. The degree of spasticity ranged from grade 1 to 2 hypertonia according to Modified Ashwarth Scale (MAS)
3. Level II and III on GMFCS-ER
4. They were able to understand and follow verbal instructions
Exclusion Criteria
7 Years
10 Years
ALL
Yes
Sponsors
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Badr University
OTHER
Responsible Party
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hanaa mohsen
lecturer,department of physical therapy for pediatrics and pediatric surgery, badr university in cairo
Locations
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Hanaa
Cairo, , Egypt
Countries
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Other Identifiers
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Hana 5
Identifier Type: -
Identifier Source: org_study_id
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