- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06289231
The Use of Artificial Intelligence (AI) for Gait Analysis
March 1, 2024 updated by: Gdansk University of Physical Education and Sport
Possibility of Using a Mobile Application for Three-plane Gait Analysis.
The main purpose of this study will be to assess the consistency and reliability of measurements made using the Vicon three-plane gait analysis device (Vicon Motion Capture System Ltd, Oxford, UK) and a mobile application based on image recognition technology with the help of artificial intelligence.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
The study will involve 50 healthy, physically active people aged 20-25.
The participants will be subjected to movement analysis using the Vicon three-plane gait analysis system using reflective markers.
Each of them will make 6 walks at their natural pace along a 10 m long path, during which a three-plane image of their walking will be recorded by the Vicon system.
Additionally, during the examination, video recording of the full gait cycle in the sagittal plane from both sides, in the front plane from both sides and at an angle of 30, 45 and 60 degrees will be made using a smartphone camera.
The recorded gait cycle using the camera will be analyzed in an image recognition application, which will generate angular values of the lower limb joints.
First, the values generated by the Vicon system and the application from the sagittal plane recording will be compared.
Then, the consistency of the values generated by the application from the recordings in the sagittal plane on both sides for the same lower limb will be checked.
The last step will be to compare the compliance of the angular values from the Vicon system with the data generated in the application from recordings at angles of 60, 45, 30 and 0 degrees.
Study Type
Observational
Enrollment (Estimated)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Paulina W Ewertowska, PhD
- Phone Number: 0048 500157143
- Email: paulina.ewertowska@awf.gda.pl
Study Contact Backup
- Name: Łukasz Poniatowski
- Phone Number: 0048 535120640
- Email: lukaszponiatowski00@gmail.com
Study Locations
-
-
Pomorskie
-
Gdańsk, Pomorskie, Poland, 80-336
- Gdansk University of Physical Education and Sport
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Students of the Academy of Physical Education and Sport in Gdańsk,
Description
Inclusion Criteria:
- healthy people aged 20-25 years
Exclusion Criteria:
- orthopaedic disease
- neurological disease
- rheumatological disease
- pain in lower limbs in the last 6 months
- pain in lumbar spine in the last 6 months
- surgeries of lower limbs in the last 6 months
- surgeries of spine in the last 6 months
- musculoskeletal injuries in the lower limbs in the last 6 months
- musculoskeletal injuries in the lumbar spine in the last 6 months
- overweight and obesity, determined on the basis of the BMI value
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Gait analysis by the Vicon system
Time Frame: 45 minutes
|
To perform gait analysis, it is necessary to attach reflective markers to the subject at specific anthropometric points.
Participants will be asked to walk barefoot in a relaxed manner at a self-selected comfort speed through a 10-meter path (6 repetitions of walking).
Each passage through the path will be recorded using the Vicon three-plane gait assessment system, which generates angular values of the ankle, knee and hip joints (degree).
|
45 minutes
|
Gait analysis by the mobile image recognition application
Time Frame: 45 minutes
|
During the gait analysis using the Vicon system, video recording of the full gait cycle in the sagittal plane from both sides, in the front plane from both sides and at an angle of 30, 45 and 60 degrees will be made using a smartphone camera.
The recorded gait cycle using the camera will be analyzed in an image recognition application, which will generate angular values of the lower limb joints (degree).
|
45 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Paulina W Ewertowska, PhD, Gdansk University of Physical Education and Sport
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 1, 2024
Primary Completion (Estimated)
July 1, 2024
Study Completion (Estimated)
August 1, 2024
Study Registration Dates
First Submitted
February 19, 2024
First Submitted That Met QC Criteria
February 28, 2024
First Posted (Actual)
March 1, 2024
Study Record Updates
Last Update Posted (Estimated)
March 4, 2024
Last Update Submitted That Met QC Criteria
March 1, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- AWFiS/2023_5_PE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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