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Completed

NCT Number: NCT03023579

The Star Excursion Balance Test: Analysis of Children With Cerebral Palsy

PURPOSE: The investigators estimated the reliability, standard error of measurement (SEM), and minimum detectable change (MDC) of the star excursion balance test (SEBT) in children with cerebral palsy (CP).

METHODS: Eight children with CP (four boys and four girls, sixteen legs) participated in this study. Each child carried out the SEBT and was assessed by two examiners. To determine intra-rater reliability, the investigators calculated the intra-class correlation coefficient (ICC) model (3,3). The investigators also calculated the ICC model (2,3) to determine the inter-rater reliability.

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Key information

Conditions

Age range

4 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • were aged between 4 and 12 years,
  • had a status above level II on the Gross Motor Function Classification System (GMFCS),
  • were able to understand instructions from the rater, and

Exclusion criteria

  • had history of fracture or sprain of the lower limbs over the previous 12 months.

Treatment and study plan

The star excursion balance test

Other

Primary outcomes

  1. The star excursion balance test

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Inje University

Other

Registry information

Important dates

Study start
2016
Primary completion
2016
First posted
Jan 18, 2017
Registry last updated
Jan 18, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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