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RecruitingNCT05751408

Technical Evaluation of Commercial IMUs Within Clinical Gait Analysis

Technical Evaluation of Commercial IMUs Within Clinical Gait Analysis in Adult Patients With Neurological Disorders

Status
Recruiting
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
Roessingh Research and Development · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A standard clinical gait analysis consists of observing walking with video (2D) or advanced equipment (VICON 3D). This 3D method provides detailed information about the gait pattern, but is time-consuming in implementation and data analysis. There are commercial 3D systems on the market that are used in healthy individuals and in sports. These so-called Inertial Measurement Units (IMUs) may also be suitable for use in the clinic. In this research protocol, the aim is to test the usability of commercial sensors and technically compare them with standard clinical 3D gait analysis in adult patients with a neurological disorder.

Detailed description

Measurements will include subjects that perform routine clinical 3D gait analysis because of a clinical question related to stiff knee gait or surgical intervention of the foot. During routine clinical gait analysis, Vicon markers and EMG-measurements of specified muscles is included. IMU-sensors will be included to this routine measurements to measure accelorometer, gyroscope and magnetometer data of both feet, both upper and lower legs, the sternum and the sacrum.

Conditions

Interventions

TypeNameDescription
PROCEDUREgait analysis using 3D (Vicon) and IMU (Movella)Subjects are measured using Vicon 3D analysis, combined with IMU-sensors

Timeline

Start date
2023-01-25
Primary completion
2025-06-01
Completion
2025-06-01
First posted
2023-03-02
Last updated
2024-04-19

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT05751408. Inclusion in this directory is not an endorsement.