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Not yet recruiting NCT07451509

Implementation of Machine Learning Into Optical Pedography

Observational Healthy Foot Pressure Area Pressure Distribution

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Optical pedography.
Who it may be relevant to
Registry conditions: Healthy, Foot, Pressure Area, Pressure Distribution. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Czechia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Implementing Machine Learning Into Optical Pedography: Development and Validation of a Novel Instrument: a Validation Study

Overview

This study aims to evaluate the validity and reliability of a proposed plantar pressure assessment intrument based on an implementation of machine learning into optical pedography.

Detailed description

This study aims to evaluate the validity and reliability of a proposed plantar pressure assessment intrument based on an implementation of machine learning into optical pedography. The whole process will be divided into distinct steps required for the targeted outcome, which includes:

1. collecting visual data (podoscope foot pictures) and training a segmentation machine learning-based algorithm designed for recognizing only feet area, a total of atleast 30 participants performing 9 different standing positions - over 270 usable pictures for training and functionality validation 2. collecting personal, visual and pressure data (participant weight, podoscope foot pictures, pedobarographic platform measurements) and training a machine/deep learning-based model designed for feet pressure distribution areas identification and quantification, a total of estimated 60 participants undergoing 5 alternating, as similar as possible, measurements on podoscope and pedobarographic platform 3. evaluating the validity and reliability of a new plantar pressure measuring instrument following the same imaging procedure as described in step 2, a total of estimated 60 participants

Interventions

  • Diagnostic test Optical pedography
    Comparison of 5 alternating measures taken on podoscope and pedobarographic platform

Primary outcome measures

  • Criterion validity of foot area measurement [Time frame: Day 1]
  • Criterion validity of peak plantar pressure distribution [Time frame: Day 1]
  • Intrasession reliability of foot area measurement [Time frame: Day 1]
  • Intrasession reliability of mean peak pressure [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • A healthy individual with no absence of lower extremity
  • Aged ≥18 years
  • Willingness to participate and ability to follow the assessors instructions.

Exclusion criteria

  • Presence of foot diseases alternating foot contact area
  • Cognitive or psychiatric disorders limiting cooperation
  • Lack of informed consent or non-compliance during imaging

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Czechia · 1 center
  • Faculty of Health Sciences, Palacký University Olomouc, Czech Republic — Olomouc

Identifiers

NCT: NCT07451509 · UPOL-340091/1030S-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗