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Treadmill interventions in children under six years of age at risk of neuromotor delay

Abstract

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Background

Delayed motor development may occur in children with Down syndrome, cerebral palsy, general developmental delay or children born preterm. It limits the child's exploration of the environment and can hinder cognitive and social‐emotional development. Literature suggests that task‐specific training, such as locomotor treadmill training, facilitates motor development.

Objectives

To assess the effectiveness of treadmill interventions on locomotor development in children with delayed ambulation or in pre‐ambulatory children (or both), who are under six years of age and who are at risk for neuromotor delay.

Search methods

In May 2017, we searched CENTRAL, MEDLINE, Embase, six other databases and a number of trials registers. We also searched the reference lists of relevant studies and systematic reviews.

Selection criteria

We included randomised controlled trials (RCTs) and quasi‐RCTs that evaluated the effect of treadmill intervention in the target population.

Data collection and analysis

Four authors independently extracted the data. Outcome parameters were structured according to the International Classification of Functioning, Disability and Health model.

Main results

This is an update of a Cochrane review from 2011, which included five trials. This update includes seven studies on treadmill intervention in 175 children: 104 were allocated to treadmill groups, and 71 were controls. The studies varied in population (children with Down syndrome, cerebral palsy, developmental delay or at moderate risk for neuromotor delay); comparison type (treadmill versus no treadmill; treadmill with versus without orthoses; high‐ versus low‐intensity training); study duration, and assessed outcomes. Due to the diversity of the studies, only data from five studies were used in meta‐analyses for five outcomes: age of independent walking onset, overall gross motor function, gross motor function related to standing and walking, and gait velocity. GRADE assessments of quality of the evidence ranged from high to very low.

The effects of treadmill intervention on independent walking onset compared to no treadmill intervention was population dependent, but showed no overall effect (mean difference (MD) ‐2.08, 95% confidence intervals (CI) ‐5.38 to 1.22, 2 studies, 58 children; moderate‐quality evidence): 30 children with Down syndrome benefited from treadmill training (MD ‐4.00, 95% CI ‐6.96 to ‐1.04), but 28 children at moderate risk of developmental delay did not (MD ‐0.60, 95% CI ‐2.34 to 1.14). We found no evidence regarding walking onset in two studies that compared treadmill intervention with and without orthotics in 17 children (MD 0.10, 95% CI ‐5.96 to 6.16), and high‐ versus low‐intensity treadmill interventions in 30 children with Down syndrome (MD ‐2.13, 95% ‐4.96 to 0.70).

Treadmill intervention did not improve overall gross motor function (MD 0.88, 95% CI ‐4.54 to 6.30, 2 studies, 36 children; moderate‐quality evidence) or gross motor skills related to standing (MD 5.41, 95% CI ‐1.64 to 12.43, 2 studies, 32 children; low‐quality evidence), and had a negligible improvement in gross motor skills related to walking (MD 4.51, 95% CI 0.29 to 8.73, 2 studies, 32 children; low‐quality evidence). It led to improved walking skills in 20 ambulatory children with developmental delay (MD 7.60, 95% CI 0.88 to 14.32, 1 study) and favourable gross motor skills in 12 children with cerebral palsy (MD 8.00, 95% CI 3.18 to 12.82). A study which compared treadmill intervention with and without orthotics in 17 children with Down syndrome suggested that adding orthotics might hinder overall gross motor progress (MD ‐8.40, 95% CI ‐14.55 to ‐2.25).

Overall, treadmill intervention showed a very small increase in walking speed compared to no treadmill intervention (MD 0.23, 95% CI 0.08 to 0.37, 2 studies, 32 children; high‐quality evidence). Treadmill intervention increased walking speed in 20 ambulatory children with developmental delay (MD 0.25, 95% CI 0.08 to 0.42), but not in 12 children with cerebral palsy (MD 0.18, 95% CI ‐0.09 to 0.45).

Authors' conclusions

This update of the review from 2011 provides additional evidence of the efficacy of treadmill intervention for certain groups of children up to six years of age, but power to find significant results still remains limited. The current findings indicate that treadmill intervention may accelerate the development of independent walking in children with Down syndrome and may accelerate motor skill attainment in children with cerebral palsy and general developmental delay. Future research should first confirm these findings with larger and better designed studies, especially for infants with cerebral palsy and developmental delay. Once efficacy is established, research should examine the optimal dosage of treadmill intervention in these populations.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Plain language summary

Treadmill interventions in children under six years of age at risk of delay in motor skills

Review question

This is an update of the review published in 2011, which examined the effect of treadmill interventions on children below six years of age at risk of delay in motor skills.

Background

Helping children with motor delays to walk is often the focus of therapeutic intervention. Some literature suggests that treadmill training could provide an opportunity for children to walk with support for sufficient periods of time to enhance motor learning. This review examined existing evidence about treadmill interventions in young children with neuromotor impairment.

Search date

The evidence is current to May 2017.

Study characteristics

We included seven studies on treadmill intervention on 175 children with Down syndrome, cerebral palsy, general developmental delay or children with moderate risk for delay. Studies used home‐based or clinic‐based treadmill protocols, ranging in duration from six weeks to several months, or until the children walked independently.

Treadmill training versus no treadmill training was compared in five studies, including 117 children with one of the above mentioned risks. Treadmill training with or without orthotics (braces) was examined in 22 children with Down syndrome. High‐intensity versus low‐intensity treadmill training was compared in 36 children with Down syndrome.

Key results

Compared to no treadmill intervention, treadmill training helped 30 children with Down syndrome to walk earlier, but did not help 28 infants at moderate risk for developmental delay.

Overall, treadmill intervention did not improve overall gross motor function or gross motor skills related to standing. One study, which compared treadmill intervention with and without orthotics in 17 children with Down syndrome, suggested that adding orthotics might hinder gross motor progress. However, 20 ambulatory children with developmental delay, who engaged in treadmill training at preschool, improved walking skills. Twelve children with cerebral palsy, who received intensive treadmill training, showed faster achievement of motor milestones than children without treadmill training.

None of the studies reported problems or injuries from the treadmill training.

Overall, support for the intervention is limited. Confirmation from larger studies is necessary. Once efficacy of the intervention is established, optimal dosage research is needed.

Use of statistics

Statistical analysis was only performed on similar outcomes across studies.

Quality of the evidence

Standardized assessment for quality of evidence ranged from high to very low. Quality of evidence was determined by the number of children studied, completeness of the data, and random group assignment.