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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05210127
Other study ID # SKE 01-42/2021
Secondary ID
Status Not yet recruiting
Phase Phase 1
First received
Last updated
Start date June 1, 2022
Est. completion date June 1, 2025

Study information

Verified date November 2021
Source Józef Pilsudski University of Physical Education
Contact Mateusz Baran
Phone 500220003
Email mateusz.baran.93@wp.pl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to identify the impact of CFS foot muscle training on time-space parameters, anthropometric parameters and bioelectrical activity (EMG) of the foot muscles during walking and to develop an algorithm for an effective therapeutic method in patients after hallux valgus correction. Achieving the purpose of the research will contribute to the answer to the following research questions: - Does the CFS therapy used significantly change the arch of the foot in HV patients compared to the control group? - Does the CFS therapy used significantly improve gait characteristics after HV surgery in relation to the control group? - Does muscle stimulation and the moment of their activation differ in groups in which different therapies have been used? - Will the results of the questionnaires and scale be significantly different in both groups?


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date June 1, 2025
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 55 Years
Eligibility Inclusion Criteria: - hallux valgus deformity - surgical procedure - voluntary consent to the study Exclusion Criteria: - lack of consent to research - other deformation and operations of the foot - pain after the surgery which prevents experimental procedure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Scarf osteotomy for Hallux Valgus deformity
An experiment of foot muscle strength and activation, during gate phases after hallux valgus correction with the use of core foot system protocol

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Józef Pilsudski University of Physical Education

Outcome

Type Measure Description Time frame Safety issue
Primary American Orthopaedic Foot and Ankle Scale for first metatarsophalangeal joint Orthopaedic Scale to describe function and problems with first metatarsophalangeal joint 8 weeks
Primary The 36-Item Short Form Survey (SF-36) The SF-36 is often used as a measure of a person or population's quality of life (QOL) 8 weeks
Primary Zebris Medical System The plantar pressure distribution measurement systems 8 weeks
Primary EMG test Electromyography (EMG) measures muscle response or electrical activity in response to a nerve's stimulation of the muscle 8 weeks
Primary Podoscope test A diagnostic device that allows the assessment of the sole of the foot while standing 8 weeks
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