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Training and Testing Database for IMU Based Gait Analysis Methods
Training and Testing Database for IMU Based Gait Analysis Methods

NCT07236008

RecruitingN/A

Sponsor: Vrije Universiteit Brussel

Conditions: Healthy Subjects or Volunteers

Countries: Belgium

The goal of this study is to establish a high-quality, synchronised dataset of gait events (GE) by simultaneously collecting inertial measurement unit (IMU) data and validated ground truth detections using a Vicon motion capture system. The primary objective is to address existing limitations in GE detection - such as poor generalisability, limited data diversity, and lack of precise synchronisation - through a rigorous protocol that ensures accuracy and transparency. The experiment is structured in three phases. First, Vicon-derived GE will be validated and refined using complementary modalities (force plates and video recordings). Next, deep learning (DL) algorithms will be developed and evaluated for GE detection directly from IMU data, with Vicon annotations serving as ground truth. Finally, the impact of differences in GE timing on spatiotemporal gait parameters (SGP) will be analysed to assess the feasibility of using IMU-only systems for reliable gait analysis. By achieving these objectives, the study aims to improve the accuracy of GE detection from wearable sensors and enable more accessible, scalable, and reliable gait analysis outside the laboratory environment.

Eligibility overview

Sex: ALL

Age: 18 Years to 65 Years

Healthy volunteers: Yes

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

* Healthy subjects with no motor impairments that disrupt the walking pattern.
* No history of pain in the lower limbs in the past 6 months.
* No history of lower limbs injuries/surgeries in the past 6 months.
* Language: Dutch and/or English and/or French speakers.
* Age 18-65 years old
* Subjects must be able to understand the instructions and to answer questions. Additionally, they should be able to; signal pain, fear, discomfort; give inform consent.

Exclusion Criteria:

* Persons with comorbidity that could hinder the study (e.g.: unstable cardiovascular system disorders, lung disorders, severe osteoporosis).
* Individuals with metal implants or skin conditions that would make sensor or marker placement difficult.
Locations (1)
  • Brussels, Belgium, Belgium