Efficacy of Combination Taping Technique vs Ankle Foot Orthosis on Improving Gait Parameters in Cerebral Palsy

NCT ID: NCT04839939

Last Updated: 2021-04-14

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

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-01

Study Completion Date

2021-03-30

Brief Summary

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Gait in children with spastic CP is often characterized by abnormal gait kinematics as knee flexion and equines foot which associated with such gait deviations, an elevated walking energy cost is often observed which may contribute to activity limitations.

The ability to maintain proper joint alignment of the lower extremity, and control the position of the foot in standing and walking is a critical treatment objective for gait in children with cerebral palsy. Lower extremity orthoses, such as ankle-foot orthoses (AFOs) are widely recommended in children with spastic cerebral palsy to prevent the development or progression of this deformity and to improve the dynamic efficiency of the child's gait. The use of Kinesio taping in pediatric rehabilitation becomes increasingly popular in recent years. Recent systematic reviews reported moderate evidence that Kinesiology taping is a useful adjunct to physiotherapy intervention in higher functioning children with CP. Combination tapings is a technique first introduced by Kenzo Kase, in which Kinesio taping is coupled with the rigid athletic tape to maximize the treatment benefits. This approach remains briefly addressed in the literature with no prior studies has examined the effects of combination tapings in the CP pediatric population. Hypothesis: there is no difference between the effect of combining tapings and ankle-foot orthosis on spatiotemporal gait parameters in spastic cerebral palsied

Detailed Description

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This study was designed as a randomized controlled trial. The participants and their parents were given clear, detailed explanation of the proposed procedures before starting the experiment, and signed a written informed consent statement. Batterjee Medical College Research and Ethical committee reviewed and approved the study, which were conducted in compliance with the 1975 Helsinki Declaration. Thirty-six children (22 males and 14 females) with spastic diplegic cerebral palsy were enrolled in this study. The children were randomly assigned into two study groups (A \& B), and a control group (C). Randomization was done by asking each child to pick up an index card out of a box that contains 36 cards (12 cards for each group) to determine which group participants would be in. Measurements were taken in two occasions, baseline, and four weeks after application of the intervention. Spatiotemporal Gait parameters were measured as per the published guidelines using the GAITRite system. Parameters included were cadence, step length; stride length, single support time, double support time, and velocity were evaluated.

Conditions

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Gait Spastic Diplegia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Control Group

Children in this group received conventional physical therapy program in form of Stretching for tight muscles, weak muscles Strengthening, Postural reactions training, Proprioceptive training, and Walking training were all part of the treatment plan, which was based on the neurodevelopmental approach.

Group Type ACTIVE_COMPARATOR

Conventional physical therapy

Intervention Type OTHER

Stretching for tight muscles, weak muscles Strengthening, Postural reactions training, Proprioceptive training, and Walking training

AFO Group

Children in this group received the same conventional treatment plus they were provided with solid community-prescribed AFO with a wearing schedule of 6-12 hours per day. Parents were given a detailed demonstration about how to use the AFO probably and watching for areas of skin overpressure. AFO needs to be worn with a smooth, long sock underneath with the child's heel is right down in the AFO with the ankle strap and/or shoe fastened firmly.

Group Type EXPERIMENTAL

Ankle Foot Orthosis

Intervention Type OTHER

Solid prescribed AFO with a wearing schedule of 6-12 hours per day

Combination Taping Group

Children in this group received the same conventional treatment plus the combination taping technique, which was performed by one qualified physical therapist with over five years of experience. The technique started with the application of two 5-cm wide Kinesio tape "I" straps. The first strap was applied from the lateral condyle of the tibia to the base of the first metatarsal bone with the ankle joint in plantar flexion. The tape was not stretched for 5 cm from the initial site and was then stretched up to 30% for the remaining parts15. The second "I" strap While the therapist holds the ankle in dorsiflexion, he applied the distal end of the tape 10 cm below the ankle joint. With almost 70% tension, the proximal end is applied 10 cm above the ankle joint. While one hand was holding each end of the tape, the child was asked to move the joint into plantar flexion. Finally, both hands moved towards the middle of the joint to apply the remaining tape.

Group Type EXPERIMENTAL

Combination Taping

Intervention Type OTHER

Combination between elastic and inelastic taping

Interventions

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Conventional physical therapy

Stretching for tight muscles, weak muscles Strengthening, Postural reactions training, Proprioceptive training, and Walking training

Intervention Type OTHER

Ankle Foot Orthosis

Solid prescribed AFO with a wearing schedule of 6-12 hours per day

Intervention Type OTHER

Combination Taping

Combination between elastic and inelastic taping

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age range from 8 to 15 years old
* Able to stand and walk independently
* Spasticity ranged from 1 to 1+ grade according to Modified Ashworth Scale
* level I or II according to Gross Motor Function Classification System (GMFCS)
* Able to understand and follow instructions

Exclusion Criteria

* Children with previous corrective orthopedic surgery or botulinum toxin injection in the lower extremities within the previous 6 months
* Skin disease
* Epilepsy
* Mental retardation
* Visual or auditory problems
Minimum Eligible Age

8 Years

Maximum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Taif University

OTHER

Sponsor Role collaborator

Batterjee Medical College

OTHER

Sponsor Role lead

Responsible Party

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Mohamed A. Abdel Ghafar

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mohamed M. Abdel Ghafar, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Batterjee Medical College

Locations

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Fizik Center For Physiotherapy

Jeddah, , Saudi Arabia

Site Status

Countries

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Saudi Arabia

Other Identifiers

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Batterjee

Identifier Type: -

Identifier Source: org_study_id

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