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Clinical Trial Summary

Using double blind, randomized controlled design to investigate the short-term therapeutic effects of function of customized insoles on children with developmental delays


Clinical Trial Description

A total of 52 children with developmental delays will be enrolled. The participants will be randomized into two groups, including study group (with insoles) and control group (without insoles).

The participants in the study group will be evaluated at baseline, that is before the customized insoles are prescribed. All of evaluations, including physical function, balance, and quality of life will be re-evaluated up to 12 weeks after insoles wearing.

The control group will be evaluated at the baseline and up to 12 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03191006
Study type Interventional
Source Taipei Medical University
Contact Ru-Lan Hsieh, MD
Phone 228332211
Email M001052@ms.skh.org.tw
Status Not yet recruiting
Phase N/A
Start date June 24, 2017
Completion date December 31, 2017

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