The Effect of Soft Orthoses on Balance and Gait Performance in Children With Cerebral Palsy

Cerebral Palsy Clinical Trial

Official title:

The Effect of Soft Orthoses and Strapping on Balance and Gait Performance in Children With Cerebral Palsy: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04990193
• Other study ID #: 19-MED-1-0004
• Status: Completed
• Phase: N/A
• Start date: May 1, 2017
• Est. completion date: March 1, 2021

Study information

• Verified date: July 2021
• Source: Umm Al-Qura University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Most of the available studies that are relevant to motor rehabilitation for children with dyskinetic type of cerebral palsy are few and are comprised of small numbers of children. Further researches are necessary to explore new conservative therapeutic protocols and techniques that should contribute to control disorganized movement, handle postural asymmetry, maintain postural stability, and improve gait performance. Therefore, the objective of this study was to examine the effectiveness of soft orthosis and strapping system on balance, and gait performance in children with dyskinetic cerebral palsy.

Description:

Dyskinetic type of cerebral palsy typically results from extrapyramidal and basal ganglia damage. The most common dyskinetic movement disorders are choreoathetosis and dystonia. Their clinical features include fluctuation of muscle tone, involuntary and in-coordinated movement, and posture instability. These features have significant negative impacts on the children's quality of life and performance of daily activities. Management strategy for children with dyskinesia requires both medical and rehabilitative treatment. Most of the available studies that are relevant to their motor rehabilitation are few and comprised of small numbers of children. The therapeutic modalities currently used for their rehabilitation require more evidence to certain their efficacy. Moreover, further researches are necessary to explore new conservative therapeutic protocols and techniques that should correct postural instability and improve the poor mobility of these children The objective of this study was to examine the effectiveness of an orthotic undergarment which is (TheraTog orthosis), and its strapping system on balance and gait performance in children with dyskinetic cerebral palsy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: March 1, 2021
• Est. primary completion date: February 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 12 Years to 16 Years

Eligibility

Inclusion Criteria:

• Children of a confirmed diagnosis of dyskinetic cerebral palsy of choreoathetosis type were selected to participate in this study.

• Children (of both sexes) were between 12 and 16 years old were included .

• Their height and weight were more than 100 cm and 20 Kg respectively to be eligible for the evaluation process on the Biodex stability system.

• Children were able to comprehend and follow orders.

• Their gross motor development levels, as measured by Gross Motor Function Classification System, were between levels I and II.

• Throughout the study period, participating children were not subjected to any other physical therapy programs except the assigned treatment protocol.

Exclusion Criteria:

• Children were excluded from this study if they had inflexible spinal deformities interfering with spinal and limbs functional mobility.

• Children were also excluded if their skin were sensitive or inflamed to any materials used.

• Children who had seizures, perceptual disorders, visual problems, and auditory deficits did not participate as well.

Related Conditions & MeSH terms

• Cerebral Palsy

Intervention

Other:
• Conventional Physical Therapy Protocol
The conventional physical therapy protocol was designed to improve axial stability and trunk steadiness during standing and walking. The conventional therapeutic protocol for every child was 3 sessions/week for 12 consecutive weeks. Every treatment session was conducted for 2 hours with a 15-minutes rest between the two training hours.
• TheraTog orthotic undergarment with its strapping system
TheraTog orthotic undergarment with its strapping system was applied for eight hours every day for twelve consecutive weeks.

Locations

Country	Name	City	State
Saudi Arabia	Umm Al Qura University	Mecca

Sponsors (1)

Lead Sponsor	Collaborator
Umm Al-Qura University

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in the Overall Stability Indices {percentage value (%)} for Postural Stability Test (test that assessed the change in postural stability)	The Biodex Balance System was used to assess the Change in the Overall Stability Indices of the Postural Stability Test. The test includes measurement of the following indices: overall stability index, anteroposterior index and mediolateral index which represents the children's ability to control their postural balance stability in all directions. High values % represent less stability and the children had difficulty in balance control. On the other hand lower values were indicative of a better balance control.	Data was collected at baseline, and 12 weeks after intervention commencement.
Primary	Change in the Pediatric Balance Scale score (scale that assessed the change in balance performance )	The Pediatric Balance Scale is a valid and reliable test to assess and re-assess balance deficits in children with mild and moderate motor disabilities. The test includes fourteen tasks that evaluate balance abilities and motor performance in children. 0-4 is the rating score for each item, where zero is the lowest score and 56 is the highest possible score for all tasks that indicate the best balance and motor performance ever.	Data was collected at baseline, and 12 weeks after intervention commencement.
Primary	Change in the gait parameter (step length) (This parameter indicated the change of gait performance).	An electronic walkway that connected to a portable computer was used to measure the following gait parameter: step length (cm).	Data was collected at baseline, and 12 weeks after intervention commencement.
Primary	Change in the gait parameter (gait cycle time) (This parameter indicated the change of gait performance).	An electronic walkway that connected to a portable computer was used to measure the following gait parameter: gait cycle time (seconds).	Data was collected at baseline, and 12 weeks after intervention commencement.
Primary	Change in the gait parameter (cadence) (This parameter indicated the change of gait performance).	An electronic walkway that connected to a portable computer was used to measure the following gait parameter: cadence (steps/ minute).	Data was collected at baseline, and 12 weeks after intervention commencement.
Primary	Change in the gait parameter (velocity) (This parameter indicated the change of gait performance).	An electronic walkway that connected to a portable computer was used to measure the following gait parameter: velocity (meter / second).	Data was collected at baseline, and 12 weeks after intervention commencement.