Biomechanical Functional Evaluation of Plantar Pressures After Foot and Ankle Surgeries

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorIstituto Ortopedico Rizzoli

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Patients with severe postural instability

Patients with cognitive deficits

Trial design

Design model

Single group

Treatments tested in this trial

  • Plantar pressure

    Other intervention

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

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Post-surgical foot and ankle patientsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Visual Analogue Scale

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).

Time frame
At baseline (day 0)
2

Visual Analogue Scale

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).

Time frame
After 6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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