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Improving the Function of the Foot by Core Foot System (CFS) Exercise Theory in Patients After Hallux Valgus Surgical Procedure

Improving the Function of the Foot by Core Foot System (CFS) Exercise Theory in Patients After Hallux Valgus Surgery

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05210127
Enrollment
60
Registered
2022-01-27
Start date
2022-06-01
Completion date
2025-06-01
Last updated
2022-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hallux Valgus

Keywords

hallux valgus, core foot system, rehabilitation protocol

Brief 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?

Interventions

PROCEDUREScarf 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

Sponsors

Józef Piłsudski University of Physical Education
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 55 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
American Orthopaedic Foot and Ankle Scale for first metatarsophalangeal joint8 weeksOrthopaedic Scale to describe function and problems with first metatarsophalangeal joint
The 36-Item Short Form Survey (SF-36)8 weeksThe SF-36 is often used as a measure of a person or population's quality of life (QOL)
Zebris Medical System8 weeksThe plantar pressure distribution measurement systems
EMG test8 weeksElectromyography (EMG) measures muscle response or electrical activity in response to a nerve's stimulation of the muscle
Podoscope test8 weeksA diagnostic device that allows the assessment of the sole of the foot while standing

Contacts

Primary ContactMateusz Baran
mateusz.baran.93@wp.pl500220003
Backup ContactMateusz Baran
mb683@stud.awf.edu.pl500220003

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026