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Enrolling by invitation NCT06849934

Reliability of Kinovea Software for Measurement of Transtibial Amputee Knee Kinematics

— Observational Amputee Amputees

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Amputee, Amputees. Basic parameters: 18 years — 65 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
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Reliability of Kinovea Software for Measurement of Transtibial Amputee Knee Angle During Walking

Overview

The primary aim of this study was to find the reliability of Kinovea software in measuring parameters associated with sagittal plane knee kinematics during gait in transtibial amputees. The secondary objective was to calculate the absolute reliability by calculating the Standard Error of Measurement (SEM), SEM% and Minimal Detectable Change at 95% confidence interval (MDC95). The SEM value represents the extent to which a score changes during the repetition of the measurement. The MDC is the minimum change in the measurement that is considered a true change in the measured activity that is not due to error.

Primary outcome measures

  • Vİdeo Recording [Time frame: From enrollment to the end of video record (10 minutes).]

Eligibility criteria

Inclusion criteria

  • Having a unilateral below-knee (transtibial) level amputation,
  • Using a prosthesis and being able to walk with the prosthesis,
  • Body mass index less than 30,
  • No contracture in the intact or amputated knee.
  • Not having had any surgery related to the knees.

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

Healthy volunteers: No

Study design

Observational model
Case-crossover

Study locations

Turkey (Türkiye) · 1 center
  • University Health Sciences — Ankara

Identifiers

NCT: NCT06849934 · 2024-173

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗