- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05308563
Fall Risk Assessment Using Hybrid Machine Learning and Deep Learning Approaches and a Novel Posturography
Study Overview
Status
Conditions
Detailed Description
The purpose of this project is to combine a novel posturogrpahy based on HTC VIVE trackers and hybrid machine learning and deep learning algorithms to establish a set of simple, convenient and valid fall risk assessment tool. This observational and follow up study will community elderly aged over 60 years old. The investigators will collect demographic data, questionnaire surveys, traditional balance tests (Berg Balance scale, Timed-up-and-go, 30s-sit-to-stand, four-stage balance tests) and a tracker-based posturography to obtain the trunk stability parameters in different standing task. The fall risk will be classified according to self-reported falls in the past one year and verified in a 6-month follow up.
The investigators will evaluate the performance of different hybrid machine learning and deep learning algorithm to extract the important features of multiple posturographic parameters and select an optimal model. The investigators will use the receiver operating characteristic curve analysis to compute the sensitivity, specificity and accuracy of different algorithms for risk classification and also compare the performance with traditional balance assessment tools. The investigators will evaluate the correlation of these posturographic features and data obtained by other methods. Risk factors of previous falls and future falls will also analyzed.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Huey-Wen Liang
- Phone Number: 66697 +886-02-23123456
- Email: lianghw@ntu.edu.tw
Study Contact Backup
- Name: Jin-Sing Jen
- Phone Number: 67752 +886-02-23123456
- Email: ntuhpmr.4124@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- can walk in the household without device independently
Exclusion Criteria:
- with terminal disease
- with cognitive impairment to follow verbal instruction
- with neurological conditions that are associated with leg weakness
- with significant visual impairment that interferes with daily living and walking
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of fall events
Time Frame: 6 months
|
self-reported fall events according to a followup questionnaire and defined as the sudden, involuntary transfer of body to the ground and at a lower level than the previous one
|
6 months
|
Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 202112114RINA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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