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A prospective, longitudinal study of growth, nutrition and sedentary behaviour in young children with cerebral palsy to measure growth, dietary intake, physical activity, participation, health resource use and quality of life

A prospective, longitudinal study of growth, nutrition and sedentary behaviour in young children with cerebral palsy to measure growth, dietary intake, physical activity, participation, health resource use and quality of life

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12611000616976
Enrollment
182
Registered
2011-06-16
Start date
2009-04-01
Completion date
2014-03-21
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

This population based longitudinal study of children with CP from the age of 18 months to 5 years will permit the first comprehensive evaluation of the impact of functional attainment and lifestyle factors (dietary intake and habitual physical activity) on growth, body composition and nutritional status. This study will enable more accurate prediction of the early natural history of nutritional and growth problems in young children with CP linked to activity levels and health outcomes.

Interventions

Growth (height, length, segmental length), body composition (percent body fat) nutrition (3 day weighed food record), physical activity (physical activity monitor), health outcomes (questionnaire), participation (questionnaire) and health resource use (questionnaire) will be measured at 18months of age, 3 years of age and 5 years of age.

Sponsors

University of Queensland
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
18 Months to 62 Months
Healthy volunteers
No

Inclusion criteria

All Queensland born children diagnosed with CP, born between 1st September 2006 and 31st December, 2009. We define CP as a group of permanent disorders of movement and posture that are attributed to non-progressive disturbances that occurred in the developing foetal or infant brain. The characteristic signs are spasticity, movement disorders, muscle weakness, ataxia and rigidity.

Exclusion criteria

Children with a progressive or neurodegenerative lesion will be excluded from the study.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 25, 2026