Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID06090357

Biomechanical Functional Evaluation of Plantar Pressures After Foot and Ankle Surgeries

Led by Istituto Ortopedico Rizzoli · Updated on 2025-07-18

100

Participants Needed

1

Research Sites

114 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how different surgical treatments for foot and ankle problems affect plantar pressures as a measure of functional and biomechanical recovery. While many surgical outcome assessments focus on pain, function, deformity correction, and X-rays, this study is the first to specifically evaluate plantar pressures after surgery. Biomechanical evaluations also include tests like gait analysis, balance measurements, joint movement tracking, and muscle activity assessments. Participants will undergo biomechanical functional assessments using specialized equipment such as a baropodometric platform and inertial sensors. These tests analyze gait, stabilometry, joint kinematics and kinetics, and muscle strength. The study follows patients who have had foot or ankle surgery and includes a 6-month follow-up period to observe changes in plantar pressure and other functional outcomes. During the study, researchers will measure pain levels using the Visual Analogue Scale at the start and after 6 months. The study requires participants to attend follow-up visits at the institute. The main goal is to understand how plantar pressures change over time after surgery, providing insight into functional recovery. Patients with severe postural instability or cognitive deficits are excluded to ensure accurate assessments.

CONDITIONS

Brief Title

Biomechanical Functional Evaluation of Plantar Pressures After Foot and Ankle Surgeries

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • Patients with severe postural instability
  • Patients with cognitive deficits

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Day 0

Participants undergo foot and ankle surgery followed by immediate post-operative assessments.

1 visit (in-person)

Post-operative Follow-up

Duration - 6 months

Participants attend follow-up visits to evaluate biomechanical function and plantar pressures after surgery.

1 visit at 6 months (in-person)

Trial Site Locations

Total: 1 location

1

Istituto Ortopedico Rizzoli

Bologna, Italy, 40136

Actively Recruiting

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Research Team

C

Cesare Faldini, Prof

A

Antonio Mazzotti, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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