Comparison of the Balance Board and Perceptual Motor Therapy in Children With Cerebral Palsy.

NCT ID: NCT05787132

Last Updated: 2023-04-03

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

88 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-28

Study Completion Date

2023-08-15

Brief Summary

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Various studies have worked on the sitting balance of cerebral palsy (CP) with Gross Motor Function Classification System (GMFCS) level I-III with a sample greater than 30, there is no data available to compare the effect of a balance board and perceptual motor therapy to improve sitting in GMFCS level IV and V with a sample greater than 30. This study will add the authenticity to literature with a large sample size and affect the severity of the condition.

Detailed Description

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This study will compare the effect of balance board therapy and Perceptual motor therapy to improve sitting in children with Cerebral palsy. Previous studies have worked on the sitting balance of cerebral palsy (CP) with Gross Motor Function Classification System (GMFCS) level I-III with a sample greater than 30, there is no data available to compare the effect of a balance board and perceptual motor therapy to improve sitting in GMFC level IV and V with a sample greater than 30. This study will add the authenticity to literature with large sample size and affect the severity of the condition. In addition, the patients with diagnosed Cerebral Palsy with GMFCS levels IV and V will be benefited from this study; an exercise program will help them to improve their sitting ability. A total of 88 Cerebral palsy patients will be included by dividing them into two groups (A, B). 1 hour of exercise session will be performed three times per week for 12 weeks with a total of 36 sessions. Both groups will receive 30 minutes of conventional physical therapy. In addition, group A will receive balance board therapy in the remaining 30 minutes while Group B will receive Perceptual motor therapy in the remaining 30 minutes. Data will be collected at baseline, at 4 weeks, at 8 weeks and at 12 weeks after intervention from both groups. The sitting balance will be measured by using Gross Motor Function Measure Scale (GMFM 88) and Trunk Control Motor Scale (TCMS).

Conditions

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Cerebral Palsy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
This will be single blinded study. The data will be coded and the analyst will also be blinded.

Study Groups

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Group A (Balance Board Therapy)

30 minutes of Balance board therapy along with conventional physical therapy

Group Type EXPERIMENTAL

Balance Board therapy

Intervention Type OTHER

Balance board therapy will be performed. balance board therapy has been shown to improve the sitting balance in children with cerebral palsy

Group B (Perceptual Motor Therapy)

30 minutes of Perceptual Motor therapy along with conventional physical therapy

Group Type EXPERIMENTAL

Perceptual Motor therapy

Intervention Type OTHER

Perceptual motor therapy will be performed, it has been shown to improve dynamic sitting in children with cerebral palsy.

Interventions

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Balance Board therapy

Balance board therapy will be performed. balance board therapy has been shown to improve the sitting balance in children with cerebral palsy

Intervention Type OTHER

Perceptual Motor therapy

Perceptual motor therapy will be performed, it has been shown to improve dynamic sitting in children with cerebral palsy.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients who have been diagnosed with CP GMFC level IV and V
* Both Male/Female
* Participants with the age ranges from 1.5 years to 5 years

Exclusion Criteria

* Patients diagnosed with GMFC level I, II and III
* Participants taking botulinum toxin
* Participants diagnosed with auditory and visual impairments
* Participants diagnosed with mental impairments/ unable to understand the commands
* Participants diagnosed with any other comorbid conditions like (obesity, cardiovascular impairments)
* Participants who are not willing to participate
Minimum Eligible Age

2 Years

Maximum Eligible Age

5 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Riphah International University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Imran Amjad, PhD

Role: PRINCIPAL_INVESTIGATOR

Riphah International University

Locations

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Al-Umeed Rehabilitation Association

Karachi, Sindh, Pakistan

Site Status RECRUITING

Countries

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Pakistan

Central Contacts

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Bakhtawar Samejo, MS-NMPT

Role: CONTACT

+923042923429

Facility Contacts

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Bakhtawar Samejo, DPT

Role: primary

+923042923429

Other Identifiers

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REC/ 01347 Bakhtawar Samejo

Identifier Type: -

Identifier Source: org_study_id

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