- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06047756
Hippotherapy Versus Swiss Ball Training to Improve Trunk Control and Balance on Spastic Daiplegic Cerebral Palsy
November 18, 2025 updated by: Riphah International University
Effects of Hippotherapy Versus Swiss Ball Training to Improve Trunk Control and Balance on Spastic Daiplegic Child
To compare effect in both intervention
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In this study we will compare the effects of hippotherapy and swiss ball therapy.
Our objectives of the study are To compare the effects of hippotherapy and Swiss ball training, to improve trunk control and balance on spastic diplegic cerebral palsy
Study Type
Interventional
Enrollment (Actual)
52
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Khyberpakhtunkhuwa
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Dīr, Khyberpakhtunkhuwa, Pakistan, 25000
- Helping hand for relief and development
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:• Children (male and female)
- Age group 4 to 11 years
- Subject diagnosed with CP
- Mild Spastic Diaplegic of the lower limbs according to the modified ashworth scale grade 1 to 1+
- GMFM scale sitting balance score less than 20
- Medically stable and able to understand commands
Exclusion Criteria:• Children with mental retardation,
- Epilepsy, other associated neurological disorders, other type of cerebral palsy,
- Attention deficit hyperactivity disorder and sensory issues(poor visual or hearing acuity)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Hippotherapy
Patients suffering with diplegic therapy will perform their exercise protocols on a stationary horse.The child is seat astride the horse wearing a helmet and was encouraged to perform various activities designed to emphasize movement in a forward and upward reaching direction to encourage active postural control, trunk strength, balance and trunk/pelvic dissociation.30
minutes to 1 hour with a frequency ranging from 4 sessions per week and the total duration of horseback riding 6 weeks.
|
Patient will perform different movement of the trunk while sitting on a horse.
|
|
Active Comparator: Swiss Ball therapy
Children of second group will receive swiss ball therapy.
Position the child to sit on the ball and giving extension rotation and flexion rotation to the child.
This will facilitate trunk rotation by which the upper body is towards the weight bearing hip and away from the weight bearing hip.Training program 4 times per weeks with the treatment session of 30 minutes for 6 weeks duration
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Patient will perform movements of trunk on swiss ball
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trunk Control Measurement Scale
Time Frame: 6 weeks
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Changes from Baseline The TCMS scale assesses seated trunk control in three dimensions.
The maximum score is 58 points where 20 points correspond to static balance, 28 to selective movement control, and 10 to the ability to perform dynamic reaching
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6 weeks
|
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Pediatric Balance Scale
Time Frame: 6 weeks
|
Changes from Baseline Pediatric Balance Scale is a modified version of the Berg Balance Scale that is used to assess functional balance skills in school-aged children.
The scale consists of 14 items that are scored from 0 points (lowest function) to 4 points (highest function) with a maximum score of 56 points
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6 weeks
|
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Gross Motor Functional Scale
Time Frame: 6weeks
|
Changes from baseline The Gross Motor Function Measure (GMFM) is an observational clinical tool designed to evaluate change in gross motor function in children with cerebral palsy.Greater score means higher functional level
|
6weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ayesha Bashir, MSNMPT, Riphah International University Islamabad
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2023
Primary Completion (Actual)
January 1, 2024
Study Completion (Actual)
January 1, 2024
Study Registration Dates
First Submitted
September 14, 2023
First Submitted That Met QC Criteria
September 14, 2023
First Posted (Actual)
September 21, 2023
Study Record Updates
Last Update Posted (Actual)
November 21, 2025
Last Update Submitted That Met QC Criteria
November 18, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Brain Damage, Chronic
- Cerebral Palsy
- Therapeutics
- Physical Therapy Modalities
- Patient Care
- Psychotherapy
- Behavioral Disciplines and Activities
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Animal Assisted Therapy
- Equine-Assisted Therapy
Other Study ID Numbers
- REC/00123Mehrin Wadood
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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