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Treadmill Training in Infants At-Risk for Neuromotor Delay

Infants at risk for neurodevelopmental delay with and without treadmill training: frequency of alternating steps and toe contacts

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612001060831
Enrollment
50
Registered
2012-10-04
Start date
2004-10-18
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The purpose of this study was to examine the potential benefits of treadmill training in infants who are at risk of having delays related to their movement development. In addition, previous research has suggested that there might be a relationship between how infants perform their steps on the treadmill and the age of onset of independent walking. Therefore, this has also been explored. Hypotheses: treadmill training in infants at risk for developmental delays may: a) lead to earlier onset of walking; b) increase the number of steps taken per minute; and c) improve correct foot positioning during stepping relative to an untrained control group.

Interventions

Treadmill training; frequency: 5 days/week; duration: 8 minutes/session; belt speed: 0.2m/s. The intervention started when infants were able to produce 10 supported steps on a treadmill within 1 minute trial (as long as it happened before turning 13 months corrected age, if they were to be included in this study). Treadmill training continued until the infant was observed walking 3 independent steps over ground, or the infant turned 24 months corrected age.

Sponsors

Michigan University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
6 Months to 13 Months
Healthy volunteers
No

Inclusion criteria

Mild to moderate hypo/hypertonia or developmental delay when examined by their pediatrician; no congenital musculoskeletal deficits or other genetic disorders.

Exclusion criteria

Severe hypo/hypertonia, genetic disorders such as spina bifida or Down syndrome, and genetic musculoskeletal deficits.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026