Kinesio Taping and Physiotherapeutic Exercises for Children With DCD
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|ClinicalTrials.gov Identifier: NCT04123912|
Recruitment Status : Not yet recruiting
First Posted : October 11, 2019
Last Update Posted : October 11, 2019
Aim: To investigate the effectiveness of a novel elastic taping-augmented functional movement power training (KT-FMPT) program in improving leg muscular performance, body balance, motor proficiency and functional independence in children with developmental coordination disorder (DCD).
Methodology: In this clinical trial, twenty children with DCD (aged 6-12) will be randomly assigned to either a KT-FMPT group or a placebo control group. Children in the KT-FMPT and control groups will receive elastic taping-augmented FMPT and general jogging exercise with non-elastic taping, respectively, for 12 weeks (2 hours/week). Major outcome measures: body balance and leg muscle activity will be measured via muscle sensors along with a force platform. Secondary outcome measures: leg muscle strength, motor proficiency and functional independence will be assessed by a digital dynamometer, the Movement Assessment Battery for Children-2 and Pediatric Evaluation of Disability Inventory, respectively (before- and after-intervention measurements).
Significance: The KT-FMPT group is predicted to display much better muscular and motor performances than the control group. This novel training program can be readily adopted in clinical, school, or home settings to improve functional independence in children with DCD, an outcome with positive socioeconomic implications. Moreover, study findings will inspire future research work in children with other childhood-onset disabilities.
|Condition or disease||Intervention/treatment||Phase|
|Developmental Coordination Disorder||Behavioral: Kinesio Taping - Functional Movement Power Training Behavioral: Jogging with placebo taping||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||20 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||Effect of Kinesio Taping and Functional Movement Power Training on Neuromuscular Performance, Motor Proficiency and Functional Independence in Children With Developmental Coordination Disorder: A Randomised Controlled Trial|
|Estimated Study Start Date :||January 1, 2020|
|Estimated Primary Completion Date :||December 31, 2021|
|Estimated Study Completion Date :||December 31, 2022|
|Experimental: KT-FMPT group||
Behavioral: Kinesio Taping - Functional Movement Power Training
Subjects assigned to the Kinesio Taping - Functional Movement Power Training (KT-FMPT) group will receive FMPT concurrent with KT. The FMPT protocol was developed by the research team with reference to common physiotherapeutic exercises for children with motor disabilities.9 It comprises 5 functional movement exercises and 6 lower-limb power/resistance training exercises using weights or resistance bands.
|Placebo Comparator: Control group||
Behavioral: Jogging with placebo taping
Subjects assigned to the control group will receive no FMPT or KT, but participate in a jogging intervention with placebo tape applied on their calf muscles and removed after the intervention.
- Change in leg muscle electromyographic activation onset latency time (in ms) [ Time Frame: 0 and 3 months ]Electromyographic activation onset of leg muscles
- Change in centre of pressure movement pathway in standing (in mm/cm) [ Time Frame: 0 and 3 months ]Centre of pressure movement pathway in standing
- Change in lower-extremity maximum isometric muscle strength (in kg/N) [ Time Frame: 0 and 3 months ]Maximum isometric leg muscle strength
- Change in Movement Assessment Battery for Children-2 percentile score [ Time Frame: 0 and 3 months ]Movement Assessment Battery for Children-2 percentile (motor proficiency)
- Change in Pediatric Evaluation of Disability Inventory score [ Time Frame: 0 and 3 months ]Pediatric Evaluation of Disability Inventory score (functional independence)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04123912
|University of Hong Kong|
|Hong Kong, Hong Kong|