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
22 participants
INTERVENTIONAL
2018-03-01
2019-03-01
Brief Summary
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Twenty-six patients undergoing conventional physiotherapy in a private rehabilitation center were included in the study. Patients were randomized to treatment and control groups. Study was completed with a total of 22 cases (11 for each group). At the beginning of the study, cases were evaluated with Gross Motor Function Measure-88, LEGSys Spatio-Temporal Gait Analyzer, SportKAT550tm Portable Computerized Kinesthetic Balance Device and Modified Ashworth Scale. Cases in the treatment group were treated with Compex-Winplate for 8 weeks, 3 times a week, 15 minutes a day in one session. All cases were reevaluated immediately after the treatment and 12 weeks after the treatment.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Treatment Group
Group that have received whole-body vibration treatment in addition to conventional physiotherapy
Whole-Body Vibration
Whole-Body Vibration Treatment for 3 sessions in a week for 8 weeks. Each sessions takes 15 minutes.
Conventional Physiotherapy
conventional physiotherapy for 2 sessions in a week for 8 weeks. Each sessions takes 45 minutes.
Control group
Group that have received conventional physiotherapy only
Conventional Physiotherapy
conventional physiotherapy for 2 sessions in a week for 8 weeks. Each sessions takes 45 minutes.
Interventions
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Whole-Body Vibration
Whole-Body Vibration Treatment for 3 sessions in a week for 8 weeks. Each sessions takes 15 minutes.
Conventional Physiotherapy
conventional physiotherapy for 2 sessions in a week for 8 weeks. Each sessions takes 45 minutes.
Eligibility Criteria
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Inclusion Criteria
* patients were followed-up and treated by a special rehabilitation center
* aged between 6-18 years
* patients could walk independently without using assistive devices
Exclusion Criteria
* cooperation problems
* visual or auditory disability
6 Years
18 Years
ALL
No
Sponsors
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Pamukkale University
OTHER
Responsible Party
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Fatih Tekin
Principal Investigator
Principal Investigators
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Fatih Tekin, PT PhD
Role: PRINCIPAL_INVESTIGATOR
Research Assistant
Locations
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Pamukkale University
Denizli, , Turkey (Türkiye)
Countries
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Other Identifiers
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PamukkaleUni
Identifier Type: -
Identifier Source: org_study_id
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