Diplegic Cerebral Palsy and Action Observation Training
NCT ID: NCT05209282
Last Updated: 2024-02-09
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
39 participants
INTERVENTIONAL
2022-01-01
2022-10-31
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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Grup I
Conventional physiotherapy program, Video-based action observation training
Video Based Action Observation
Individuals in this group will receive video-based action observation training in addition to the conventional physiotherapy program.
Conventional physiotherapy program
Individuals in this group will only receive a conventional physiotherapy program.
Grup II
Conventional physiotherapy program, Live Action Observation Training
Live Action Observation
Individuals in this group will receive live action observation training in addition to the conventional physiotherapy program.
Conventional physiotherapy program
Individuals in this group will only receive a conventional physiotherapy program.
Grup III
Conventional physiotherapy program
Conventional physiotherapy program
Individuals in this group will only receive a conventional physiotherapy program.
Interventions
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Video Based Action Observation
Individuals in this group will receive video-based action observation training in addition to the conventional physiotherapy program.
Live Action Observation
Individuals in this group will receive live action observation training in addition to the conventional physiotherapy program.
Conventional physiotherapy program
Individuals in this group will only receive a conventional physiotherapy program.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* To be between the ages of 5-14,
* To be at GMFCS I, II and III levels,
* To have the cognitive level to follow the instructions given by the researchers,
* IQ\> 70 (to be accessed from patient files),
* Those who do not have serious restrictions in joint movement,
Exclusion Criteria
* Not having visual impairment and visual field defect,
* Children who have had a seizure in the last 6 months or children who cannot be controlled despite seizure medication
* Those who received botulinum injections 6 months before the study.
5 Years
14 Years
ALL
No
Sponsors
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Inonu University
OTHER
Responsible Party
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Burcu Talu
Assoc.
Principal Investigators
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Burcu TALU, Assoc. Prof.
Role: PRINCIPAL_INVESTIGATOR
Inonu University
Locations
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Inonu University
Malatya, Battalgazi/MALATYA, Turkey (Türkiye)
Countries
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Other Identifiers
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2021/2663
Identifier Type: -
Identifier Source: org_study_id
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