Effects Of Kinesio Taping On Balance, Functionality, And Participation In Children With Cerebral Palsy?
NCT ID: NCT04932538
Last Updated: 2021-06-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
20 participants
INTERVENTIONAL
2020-08-15
2021-03-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
OBJECTIVE: The aim of this study was to investigate the immediate and long-term effects of Kinesio® Taping (KT) applied on the gluteus maximus and gluteus medius muscles on walking, functionality, balance, and participation in children with unilateral spastic CP.
METHOD: This study was designed as a randomized controlled trial. The study included 20 children with unilateral spastic CP: 11 in the taping group and 9 in the control group. KT was applied in the taping group for 4 weeks in addition to a physiotherapy program. The control group received only the physiotherapy program. Body structure and functions were evaluated with the Pediatric Berg Balance Scale (PBBS). Activity was evaluated with the Timed Up and Go Test (TUG), Functional Mobility Scale (FMS), Gross Motor Function Scale (GMFM-88), the BTS G-Walk Spatiotemporal Gait Analysis System. Participation was evaluated with the Canadian Occupational Performance Measure (COPM). Evaluations were made at the beginning of the study and 30 minutes after the first tape application, and at the end of 4 weeks in the taping group. The level of significance was accepted as p\<0.05.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Kinesiologic Taping on Trunk Control and Balance in Children With Cerebral Palsy
NCT07188961
Kinesio Taping in Cerebral Palsy Upper Extremity Functionality
NCT04529486
Which Taping Technique is More Effective on Balance Skills in Children With Mildly Affected Cerebral Palsy?
NCT06231108
Is Kinesio Taping Treatment Effective in Children With Cerebral Palsy?
NCT03819205
The Efficacy of Distortion Banding on Outcome Measures in Children With Cerebral Palsy
NCT05251532
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Insufficiencies in hip abduction and extension muscle function are common in CP. Excessive muscles tonus in the hip adductors and flexors and a loss of reciprocal inhibition cause a weakness in the gluteus medius and maximus. This weakness negatively affects the movement patterns of the lumbar spine, pelvis, and hip region, and also causes incorrect loadings in hip joint and abnormalities in hip biomechanics. Gait anomalies occur and pelvis stabilization is impaired. In particular, negative impacts on participation are a concern. With the physiotherapy and rehabilitation approaches, these negative effects may be minimized by facilitating the gluteal muscles. Gait training and exercises to strengthen the gluteal muscles are routinely used in the rehabilitation of CP. With these approaches, it is aimed to maximize the gait function and promote independence and participation.
The somatosensory system may be affected in unilateral spastic CP. These children often suffer sensory impairments that could affect the development of future motor skills. Kinesio Taping® (KT) is used for pediatric rehabilitation to reduce pain, facilitate or inhibit muscle activity, prevent injuries, reposition joints, aid the lymphatic system, support postural alignment, and improve proprioception.
Yasukawa et al. stated that the use of KT for children with CP might influence the cutaneous receptors of the sensory motor system, resulting in an improvement in voluntary control and coordination via a physiotherapy program. Therefore, facilitating the gluteal muscles by KT may affect walking and balance positively.
In the literature, the clinical use of KT techniques in children with CP is generally at the upper extremity. In studies in which KT is applied to the lower extremity, it is generally applied to the distal part of extremity. In addition, most of the studies have investigated the immediate effect. There are few studies investigating the effects of KT applied to the gluteus medius and gluteus maximus muscles, which are located in the proximal hip with important contributions in stabilization.
The aim of this study was to investigate the immediate and long-term effects of KT applied to the gluteus maximus and gluteus medius muscles on walking, functionality, balance, and participation in children with unilateral spastic CP.
MATERIAL AND METHODS The permission of the University Ethics Committee was received (91610558-302.08.01) and written informed consent was obtained from each participant and/or guardian.
Participants
The inclusion criteria were: having unilateral spastic CP; being in an age between 6 years and 12 years; being classified in levels I or II of the Gross Motor Function Classification System (GMFCS); having spasticity at lower extremity 2 or less according to Modified Ashworth Scale, and being able to follow and accept verbal instructions. The exclusion criteria were having any orthopedic surgery or botulinum toxin injection in the past 6 months and having allergic reactions to the adhesive compound of KT.
Procedure
This study was designed as a randomized controlled trial. Twenty children (10 girls, 10 boys) were included in the study. The children were divided into two randomized groups using a computer program. Of the 20 participants, 11 were randomized to the taping group and 9 to the control group.
Measurements In the taping group, measurements were made at the beginning of the study, 30 minutes after the first tape was applied, and at the end of the 4th week. In the control group, measurements were made at the beginning of the study and at the end of the 4th week. The BTS G-Walk Spatiotemporal Gait Analysis System was administered by the third author (S. Ö.). All other measurements were administered by the same physiotherapist (S. N. K.). Gross motor function was classified using the GMFCS.
Body Structures and Functions Body composition was evaluated by body mass index (BMI) calculated with the following formula: weight in kilograms divided by the square of the height in meters. Balance was evaluated with the Pediatric Berg Balance Scale (PBBS).
Activity functioning Functionality was assessed using the Timed Up and Go test (TUG) and the Functional Mobility Scale (FMS). The TUG measures various components such as walking speed, postural control, functional mobility, and balance . The walking ability of the participants was evaluated with the Functional Mobility Scale at 3 different distances (5 meters-indoor, 50 meters-school, 500 meters-community). Inter-observer reliability of the FMS, which can reveal changes that cannot be detected with the GMFCS, was also demonstrated. Gross motor function was assessed using dimensions D and E of the Gross Motor Function Measurement (GMFM), which consists of standing, walking, running, and jumping. The GMFM is a valid, reliable, and sensitive method, which demonstrates the change in motor functions in children with CP and other disabilities via videotape recordings.
Gait parameters were assessed using the BTS G-Walk Spatiotemporal Gait Analysis System. In this system, the analysis results of the sensor attached to the L5-S1 level of the patient was transferred to a computer via Bluetooth. This system allows gait analysis by comparing the left and right extremities with normal values, and it also enables a 3-dimensional kinematic analysis of the pelvis. The track length was preset as 10 meters. The children with CP were asked to walk the 10-meter track three times. Three measurements were averaged in the analysis.
Participation Participation was assessed using the Canadian Occupational Performance Measure (COPM). The COPM is a client-centered outcome measure to identify and prioritize everyday issues that restrict individuals' participation in everyday life.
Intervention
Every group received routine traditional physiotherapy twice a week over the period of 4 weeks. This routine traditional treatment consisted of stretching, weight bearing, functional reaching, walking, and electrotherapy. Sessions were 40 minutes. The children in the taping group were taped 6 days per week for 4 weeks. The children were checked for allergies before applying the tape. A 5-cm tape was applied and kept in position for 3 days, and the region was then left to rest for 24 hours.
KT was applied to the gluteus maximus and gluteus medius muscles. The KT muscle facilitation technique was used to support and facilitate the function of the muscles. For the gluteus maximus, a "Y" tape was used. The child was placed in a side lying position and the beginning of the tape was applied to the origin of the muscle (center of the sacrum). The leg flexed and adducted, and the first tail was applied to enclose the lower part of the gluteus maximus muscle. The second tail was applied diagonally from the sacrum to the greater trochanter. For the gluteus medius muscle, 2 "I" tapes were applied. The first tape was applied from the spina iliaca anterior superior to the greater trochanter, the second tape was applied from the spina iliaca posterior superior to the greater trochanter. During the applications, the hip was adducted and extended, and all tape ends were applied without tension.
Statistical analysis Post-hoc power analysis was performed when 20 participants (11 in the taping group, 9 in the control group) were enrolled in our study. Power analysis was conducted using G\*Power (version 3.0.10 Universitat Düsseldorf, Düsseldorf, Germany) to compare pairs of independent sample means. In the post-hoc power analysis, when the statistical significance of alpha was 5% and the confidence interval was 95%, the power of the study (1-β) was found to be 99%. The study was completed by deciding that a sufficient sample size was reached. The Statistical Package for the Social Sciences (SPSS) version 26 was used to analyze the obtained data. The level of significance was set at p\<0.05. One-sample Kolmogorov-Smirnov Tests were used to evaluate distribution of variables before test selection. Descriptive analyses are presented using medians and the interquartile ranges for the non-normally distributed and ordinal variables. In the comparison of two independent nominal variables, while the Chi-Square Test was used, the Fisher Test was preferred according to the expected values in the table cells. The Mann-Whitney U test was used to compare non-normally distributed ordinal data in independent groups. The Wilcoxon Signed Ranks Test or the Friedman was used in dependent groups. The Student's t-test was used to compare normally distributed numerical data. Repeated Measures Anova was used to compare normally distributed numerical data in more than two dependent groups. Groups were compared with each other using the paired T test.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Control Group
Every group received routine traditional physiotherapy twice a week over the period of 4 weeks. This routine traditional treatment consisted of stretching, weight bearing, functional reaching, walking, and electrotherapy.
No interventions assigned to this group
Kinesio Taping
Every group received routine traditional physiotherapy twice a week over the period of 4 weeks. This routine traditional treatment consisted of stretching, weight bearing, functional reaching, walking, and electrotherapy. Sessions were 40 minutes. The children in the taping group were taped 6 days per week for 4 weeks. The children were checked for allergies before applying the tape. A 5-cm tape was applied and kept in position for 3 days, and the region was then left to rest for 24 hours.
Kİnesio Taping
Kinesio Taping® (KT) is used for pediatric rehabilitation to reduce pain, facilitate or inhibit muscle activity, prevent injuries, reposition joints, aid the lymphatic system, support postural alignment, and improve proprioception
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Kİnesio Taping
Kinesio Taping® (KT) is used for pediatric rehabilitation to reduce pain, facilitate or inhibit muscle activity, prevent injuries, reposition joints, aid the lymphatic system, support postural alignment, and improve proprioception
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* being in an age between 6 years and 12 years;
* being classified in levels I or II of the Gross Motor Function Classification System (GMFCS); -having spasticity at lower extremity 2 or less according to Modified Ashworth Scale
* being able to follow and accept verbal instructions.
Exclusion Criteria
* having allergic reactions to the adhesive compound of Kinesio Taping
6 Years
12 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ondokuz Mayıs University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Seda Nur Kemer
Physiotherapist, Master of Science, Lecturer, Principal İnvestigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Seda Nur KEMER,PT, MSc
Samsun, Atakum, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
A7698
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.