Flat Foot Clinical Trial
Official title:
Therapeutic Effects of Customized Insoles on Children With Flat Foot
Using double blind, randomized controlled design to study the short-term therapeutic effects of customized arch-support shoe insoles to children with flat foot.
A total of 52 children with flat foot will be collected. The participants will be randomized
into two groups, including study group (insoles group) and control group (without insole
group).
All participants in the insoles group will be evaluated at baseline, that is before the
customized full-length shoe insoles are prescribed. All the evaluations, including physical
functional ability, balance, physical activity, functional performance, and quality of life
will be re-evaluated up to 12 weeks after shoe insoles wearing in the insoles group.
The control group will be evaluated at the baseline and up to 12 weeks.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Supportive Care
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