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Gait and Muscle Power Training for Children With Developmental Coordination Disorder

Rhythmical Auditory Stimulation Gait Training and Muscle Power Training for Primary School Children With Developmental Coordination Disorder: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03838614
Enrollment
76
Registered
2019-02-12
Start date
2019-06-01
Completion date
2023-12-31
Last updated
2019-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Developmental Coordination Disorder

Brief summary

Objectives: To compare the effectiveness of RAS-MPT, RAS alone, MPT alone, and usual care (as a control) for improving the overall gait performance of and reducing falls in children with developmental coordination disorder (DCD) and to explore the relationship between gait performance and falls in this population. Design: A randomized controlled trial. Sample: 76 children with DCD. Interventions: RAS-MPT, RAS alone, MPT alone, or usual care (12 weeks). Major outcomes: Outcomes will be evaluated at baseline, post-intervention, and a 6-month follow-up. Comprehensive gait analysis will produce spatiotemporal gait parameters (e.g., velocity and stride length), kinematic gait parameters (e.g., knee joint motions), and leg muscle EMG outcomes; an isokinetic test will quantify leg muscle strength and force production time; and fall histories will be obtained via interviews. Anticipated results and significance: The RAS-MPT group is predicted to display the best gait performance, which is associated with reduced fall incidents. This novel training regime can be readily adopted in school, clinical, or home settings to improve locomotor ability in children with DCD, an outcome with positive socioeconomic implications.

Interventions

BEHAVIORALRhythmical auditory stimulation gait training and muscle power training (RAS-MPT)

The RAS-MPT group will attend a 60-minute training session once a week and home exercises (twice/week) for 12 weeks. Participants will receive two levels of training within each 60-minute session: (1) RAS-treadmill training and (2) MPT.

BEHAVIORALRhythmical auditory stimulation gait training (RAS)

The RAS group will attend a 60-minute training session once a week and home exercises (twice/week) for 12 weeks. Participants will receive RAS-treadmill training repeatedly within each 60-minute session.

BEHAVIORALMuscle power training (MPT)

The MPT group will attend a 60-minute training session once a week and home exercises (twice/week) for 12 weeks. Participants will receive muscle power training repeatedly within each 60-minute session.

OTHERControls

Participants in the control group will receive no intervention during the study period, but continue with their normal daily activities and usual medical care. They will receive the same training as the RAS-MPT group after the study.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 9 Years
Healthy volunteers
No

Inclusion criteria

* 6 to 9 years old * classified as DCD according to the Diagnostic and Statistical Manual of Mental Disorders V * \< 5th percentile on the Movement Assessment Battery for Children-2 (MABC-2) * a total score of \< 46 (for children aged 6 to 7 years 11 months) or \< 55 (for children aged 8 to 9 years) on the DCD questionnaire 2007 (Chinese version) * attending a mainstream school (i.e., intelligence level within the normal range).

Exclusion criteria

* any congenital, cognitive, psychiatric (e.g., comorbid attention deficit hyperactivity disorder or autism spectrum disorder), neurological, sensory, hearing, visual, vestibular, musculoskeletal, or cardiopulmonary disorder that may affect test performance * obesity (body mass index \[BMI\] \>95th percentile) * receiving active treatment such as physiotherapy * those unable to follow instructions.

Design outcomes

Primary

MeasureTime frame
Changes in spatiotemporal gait parameter - double-limb support duration (% gait cycle)9 months
Changes in spatiotemporal gait parameter - stride length (cm)9 months
Changes in spatiotemporal gait parameter - cadence (steps/min)9 months
Changes in spatiotemporal gait parameter - stance phase duration (% gait cycle)9 months
Changes in spatiotemporal gait parameter - swing phase duration (% gait cycle)9 months
Changes in spatiotemporal gait parameter - single-limb support durations (% gait cycle)9 months
Changes in spatiotemporal gait parameter - gait velocity (m/s)9 months

Secondary

MeasureTime frameDescription
Changes in leg muscle peak electromyographic values9 monthsChanges in leg muscle peak electromyographic values (in % of maximal voluntary isometric contraction) of rectus femoris, biceps femoris, tibialis anterior, and gastrocnemius medialis muscles
Changes in leg muscle maximum strength9 monthsChanges in maximum muscle strength of knee extensors and flexors and ankle plantar flexors and dorsiflexors of the dominant leg as measured by dynamometry.
Changes in leg muscle force production time9 monthsChanges in muscle force production time of knee extensors and flexors and ankle plantar flexors and dorsiflexors of the dominant leg as measured by dynamometry.
Changes in self-reported falls9 monthsChildren and parents will report the number of falls within the study period.
Changes in kinematic gait parameters9 monthsMaximum knee and ankle angles during different gait phases

Countries

Hong Kong

Contacts

Primary ContactShirley Fong, PhD
smfong@hku.hk28315260

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026