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Recruiting NCT06554171

NCT06554171 Hippotherapy Simulators on Trunk Control and Upper Extremity Functions in Cerebral Palsy

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Clinical Trial Summary
NCT ID NCT06554171
Status Recruiting
Phase
Sponsor Firat University
Condition Cerebral Palsy
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2024-08-20
Primary Completion 2024-10-20

Trial Parameters

Condition Cerebral Palsy
Sponsor Firat University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 20
Sex ALL
Min Age 6 Years
Max Age 18 Years
Start Date 2024-08-20
Completion 2024-10-20
Interventions
Hippotherapy groupControl group

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Brief Summary

The hippotherapy simulator imitates the three-dimensional mechanical movement and walking of the horse and transfers the mechanical effect to the rider during hippotherapy. The aim of this study was to investigate the effect of exercise program with hippotherapy simulator on upper extremity functions and trunk control of individuals with cerebral palsy.All individuals diagnosed with Cerebral Palsy who agree to participate in the study and meet the inclusion criteria will be randomly divided into two groups as Study and Control Group. In addition to conventional physiotherapy, the study group will be trained in the Hippotherapy Simulature for 15 minutes a day, 5 days a week for 4 weeks.n addition to conventional physiotherapy, the control group will be allowed to sit in the Hippotherapy Simulature for 15 minutes a day, 5 days a week for 4 weeks. However, the simulator will be kept in closed position to prevent oscillations.

Eligibility Criteria

Inclusion Criteria: * Being between 6-18 years old * Being diagnosed with unilateral spastic type cerebral palsy * Voluntariness of the family and individuals to participate in the study * Being at I, II, III level according to the Hand Skills Classification System * To have the cognitive development to cooperate Exclusion Criteria: * Having undergone any orthopedic and/or neurological surgery and/or BoNT A operation within the last 6 months * Having a history of epilepsy * Hearing and/or vision loss at a level that prevents participation in the study

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