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Biomechanical Functional Evaluation of Plantar Pressures After Foot and Ankle Surgeries

Biomechanical Functional Evaluation of Plantar Pressures After Foot and Ankle Surgeries

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06090357
Enrollment
100
Registered
2023-10-19
Start date
2021-07-10
Completion date
2026-05-31
Last updated
2025-07-18

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

Conditions

Plantar Pressure

Keywords

foot, ankle, Post-operative, plantar pressure

Brief summary

The described surgical techniques for the treatment of foot and ankle pathologies are numerous. In order to objectively assess the outcomes of these procedures, evaluation methods are typically used, primarily considering pain symptoms, residual functionality, the correction of any deformities achieved, and radiographic parameters. Conversely, assessments of plantar pressures, as a potential indicator of functional and biomechanical recovery, are still not widely utilized. Biomechanical functional assessments examine specific variables, including gait analysis, stabilometry, kinematics and kinetics of joint movements, and the activation and strength of particular muscle groups. These assessments can be conducted by specialized personnel using dedicated equipment such as a baropodometric platform and inertial sensors. This study aims to, for the first time in the literature, present the results related to plantar pressures from different surgical treatments of the foot and ankle

Interventions

Biomechanical functional assessments investigate specific variables: gait analysis, stabilometry, kinematics and kinetics of joint movements, activation, and strength of specific muscle groups.

Sponsors

Istituto Ortopedico Rizzoli
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients who need to undergo surgical intervention * Patients of both sexes aged between 18-75 years * Patients who have provided their written informed consent to participate in the study * Patients who have expressed their willingness to attend the Institute for the 6-month follow-up

Exclusion criteria

* Patients with severe postural instability * Patients with cognitive deficits

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue ScaleAt baseline (day 0)Visual Analogue Scale (VAS) is one of the pain rating scales. It is unidimensional measure of pain intensity, used to record patients' pain progression, or compare pain severity between patients with similar conditions. The most simple VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured (symptom, pain, health) orientated from the left (worst) to the right (best).

Countries

Italy

Contacts

Primary ContactCesare Faldini, Prof
cesare.faldini@ior.it0516366
Backup ContactAntonio Mazzotti, PhD
antonio.mazzotti@ior.it0516366

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026