Reliability of Kinovea Software for Measurement of Transtibial Amputee Knee Kinematics

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ENROLLING_BY_INVITATION

Total Enrollment

46 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-01

Study Completion Date

2025-08-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Reliability and Validity of the 2-Minute Step Test in Patients With Knee Arthroplasty

NCT05064943

Total Knee Replacement Reliability and Validity

COMPLETED

Sagittal Knee Kinematics of Transtibial Amputee with Running Blade

NCT06586762

Amputation Prosthesis User

COMPLETED

The Effect of Different Microprocessor Knee Prostheses on Mobility and Gait Parameters in Transfemoral Amputees

NCT04966936

Amputation

UNKNOWN

Outcomes Following Total Knee Arthroplasty

NCT02364011

Osteoarthritis

COMPLETED

Evaluation of Correlations Between Different Walk Tests in Patients With Transfemoral Amputees

NCT02766387

Amputation Lower Extremity

UNKNOWN NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Amputee Amputees

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CROSSOVER

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No