- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05443893
Artificial Intelligence in Kinematics Analysis
July 1, 2022 updated by: Zhou Mouwang, Peking University Third Hospital
Application Research of Key Points Detection Technology of Artificial Intelligence in Kinematics Analysis
- Establish data sets. The private data set includes relevant parameters including video of the subject's gait and standard methods for kinematic analysis;
- Develop new models. Based on public and private data sets, the kinematic analysis model of human key point detection is further developed.
- Test the new model. By comparing the parameters with the standard method, the accuracy of the model was verified, and the kinematics analysis model of artificial intelligence with accuracy above 98% was obtained
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Artificial intelligence human key point detection model mainly has traditional algorithm, "top-down" algorithm and "bottom-up" algorithm three methods, three methods have advantages.
This project will comprehensively use the above three methods to conduct algorithm and parameter debugging in the public data set and test in the private data set, so as to obtain the most suitable human key point recognition method for gait analysis
Study Type
Observational
Enrollment (Anticipated)
30
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: Mouwang Zhou
- Phone Number: 13910092892
- Email: zhoumouwang@outlook.com
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
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Normal gait subjects and abnormal gait subjects
Description
Inclusion Criteria:
- 1. Abnormal gait.
- Can walk 6m or more independently.
- Older than 18.
Exclusion Criteria:
- Fracture may be aggravated by walking in the acute stage or early postoperative stage. Have heart, lung, liver and kidney And other serious diseases, heart function grading greater than GRADE I (NYHA), respiratory failure and other symptoms and signs or Check the results.
- The mental and psychological state cannot cooperate with the completion of the experiment.
- High risk of falls (Berg score ≤20)
- Gait kinematics analysis equipment cannot be used together.
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
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Normal subjects
Gait analysis with artificial intelligence and traditional methods
|
Artificial intelligence human key point detection model mainly has traditional algorithm, "top-down" algorithm and "bottom-up" algorithm three methods, three methods have advantages.
This project will comprehensively use the above three methods to conduct algorithm and parameter debugging in the public data set and test in the private data set, so as to obtain the most suitable human key point recognition method for gait analysis
|
|
Subjects with abnormal gait
Gait analysis with artificial intelligence and traditional methods
|
Artificial intelligence human key point detection model mainly has traditional algorithm, "top-down" algorithm and "bottom-up" algorithm three methods, three methods have advantages.
This project will comprehensively use the above three methods to conduct algorithm and parameter debugging in the public data set and test in the private data set, so as to obtain the most suitable human key point recognition method for gait analysis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gait related parameters
Time Frame: 30mins
|
Step frequency/pace/gait cycle/step length
|
30mins
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Anticipated)
July 10, 2022
Primary Completion (Anticipated)
July 29, 2022
Study Completion (Anticipated)
August 30, 2022
Study Registration Dates
First Submitted
June 3, 2022
First Submitted That Met QC Criteria
July 1, 2022
First Posted (Actual)
July 5, 2022
Study Record Updates
Last Update Posted (Actual)
July 5, 2022
Last Update Submitted That Met QC Criteria
July 1, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- M2021231
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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