The Effects of Functional Strengthening in Spastic Cerebral Palsy
NCT ID: NCT03901703
Last Updated: 2019-07-30
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
27 participants
INTERVENTIONAL
2019-01-12
2019-05-30
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
DOUBLE
Study Groups
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Dorsiflexor Muscle Strengthening Group
The children in this group will receive functional exercises aiming to strengthen their dorsiflexor muscles alongside standard functional progressive strengthening exercises.
Physiotherapy and Rehabilitation
The children in each group will receive 6 weeks of functional strengthening exercises targeting each muscle group according to the arm they are included in.
Plantarflexor Muscle Strengthening Group
The children in this group will receive functional exercises aiming to strengthen their plantarflexor muscles alongside standard functional progressive strengthening exercises.
Physiotherapy and Rehabilitation
The children in each group will receive 6 weeks of functional strengthening exercises targeting each muscle group according to the arm they are included in.
Dorsiflexor and Plantarflexor Muscle strengthening Group
The children in this group will receive functional exercises aiming to strengthen both their dorsiflexor and plantarflexor muscles alongside standard functional progressive strengthening exercises.
Physiotherapy and Rehabilitation
The children in each group will receive 6 weeks of functional strengthening exercises targeting each muscle group according to the arm they are included in.
Interventions
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Physiotherapy and Rehabilitation
The children in each group will receive 6 weeks of functional strengthening exercises targeting each muscle group according to the arm they are included in.
Eligibility Criteria
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Inclusion Criteria
* Being between 5-15 years old,
* Having a diagnosis of Spastic Cerebral Palsy,
* Being level I-II according to GMFCS,
Exclusion Criteria
* Refusing to participate in the study,
* Having an orthopedic disorder or systemic illness which prevents movement in the lower extremities,
* Having a Botulinum toxin application in the last 3 months
5 Years
15 Years
ALL
No
Sponsors
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Melek Volkan Yazici
OTHER
Responsible Party
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Melek Volkan Yazici
Principle Investigator
Principal Investigators
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Bulent Elbasan, Assoc. Prof.
Role: STUDY_DIRECTOR
Gazi University
Locations
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Gazi University
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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465426
Identifier Type: -
Identifier Source: org_study_id
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