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The effect of kinsiotaping in the subjects with hallux valgus

Phase 2
Recruiting
Conditions
Hallux valgus deformity.
Hallux valgus (acquired), unspecified foot
M20.10
Registration Number
IRCT20150602022539N7
Lead Sponsor
Semnan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Volunteers aged between 20 and 40 years old
Subjects with moderate hallux valgus

Exclusion Criteria

Unwillingness to participate in the project
Mild and severe hallux valgus
Any traumatic, inflammatory and infectious pathology in the lower extremity
Any deformity of foot and toes such as club toe and hammer toe
Problems with visiual, auditory and vestibular system
Neuromuscular deficit
Inability to understand the test procedure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Displacement of center of pressure. Timepoint: Before and after 10 days intervention. Method of measurement: Millimeter.;Visual Analogue Scale (VAS). Timepoint: Before and after 10 days intervention. Method of measurement: Millimeter.
Secondary Outcome Measures
NameTimeMethod
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