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Clinical Trials in Turkey / NCT06849934
Enrolling by invitation Observational

Reliability of Kinovea Software for Measurement of Transtibial Amputee Knee Kinematics

NCT06849934 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2024-12-01
Last updated
2025-02-27

Condition(s) studied

AmputeeAmputees

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Health Sciences Ankara Turkey (Türkiye)

More Saglik Bilimleri Universitesi trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06849934 on ClinicalTrials.gov ↗ ← All trials in Turkey