- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06785792
Artificial Intelligence-Assisted Posture Applicatıon
Validity and Reliability of Artificial Intelligence-Assisted Posture Applicatıon in Young Adults
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Özlem Çinar Özdemir, Prof.Dr
- Phone Number: +905326062346
- Email: ozlemcinarozdemir@gmail.com
Study Locations
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Karabağlar/İzmir
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İzmir, Karabağlar/İzmir, Turkey, 35140
- Recruiting
- Izmir Democracy University
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Contact:
- Özlem Çinar Özdemir, Prof.Dr
- Phone Number: +905326062346
- Email: ozlemcinarozdemir@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
The population of the research consists of young adult individuals in the general Turkish population, and the research sample consists of young adult individuals in the Turkish population who volunteered to participate in the research. There is only one research group consisting of volunteer individuals. There is only one research group within the scope of the study.
Data will be collected from individuals face to face. Individuals who meet the inclusion criteria and volunteer will be evaluated simultaneously by 3 expert physiotherapists on consecutive days (3 days) at the same time, with 3 repetitions using observational posture analysis, New York posture scale and artificial intelligence-supported posture application.
Description
Inclusion Criteria:
- Young adult individuals between the ages of 18-39
- Individuals who volunteer to participate in the study
- Individuals who are Turkish citizens, reside in Turkey and have been in Turkey for at least 1 month before and during the study period
- Individuals who can communicate in written and verbal Turkish
Exclusion Criteria:
- Individuals with any physical or mental disability and/or cognitive impairment
- Pregnant women
- Individuals with orthopedic, neurological, vestibular diseases that may affect walking and balance functions
- Individuals with neuromuscular system diseases or diseases that will prevent postural control measurements (vertigo, neuropathy, etc.) or those using medication
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Study Group
The population of the research consists of young adult individuals in the general Turkish population, and the research sample consists of young adult individuals in the Turkish population who volunteered to participate in the research.
There is only one research group consisting of volunteer individuals.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Posture Evaluation System (Fizyosoft™ Becure Posture System)
Time Frame: Individuals who meet theinclusion criteria and volunteer will be evaluated simultaneously by 3 expert physiotherapists on consecutive days (3 days) at the same time, with 3 repetitions using Posture Evaluation System (Fizyosoft™ Becure Posture System).
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Becure Posture is an artificial intelligence-supported technological solution that allows individuals to perform posture analysis, can be used via mobile devices or computer applications.
The purpose of the application is to perform posture analysis by adding photographs of clients or patients, to provide analysis by physically taking their photographs, to automatically determine joint points with artificial intelligence support and to enable users to manually edit these points when needed.
It also allows users to receive reports.
The application is licensed and can be accessed from AppleStore or PlayStore after obtaining the license.
After logging in to the account, a total of 4 photos must be uploaded to the page that opens, including the name and surname, in order to evaluate the posture: anterior, posterior, right lateral and left lateral.
After the photo is uploaded, a report is printed out in which the detailed posture analysis of the upper and lower extremities is performed.
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Individuals who meet theinclusion criteria and volunteer will be evaluated simultaneously by 3 expert physiotherapists on consecutive days (3 days) at the same time, with 3 repetitions using Posture Evaluation System (Fizyosoft™ Becure Posture System).
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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New York Posture Assessment
Time Frame: Individuals who meet theinclusion criteria and volunteer will be evaluated simultaneously by 3 expert physiotherapists on consecutive days (3 days) at the same time, with 3 repetitions using New York Posture Assessment.
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NYPD evaluates the correct and incorrect alignment of various body parts of a person in an anatomical position using a quantitative approach.
A scoring system is used in the assessment.
In the posture scoring, 5 points are given if it is correct, 3 points if there is a moderate disorder and 1 point if there is a high degree of disorder.
The total score obtained as a result of the scoring is a maximum of 65 and a minimum of 13.
In the developed standard evaluation criteria, if the total score is ≥45, it is defined as very good, 40-44 as good, 30-39 as medium, 20-29 as weak, and ≤19 as bad.
A high score indicates that the posture is correct.
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Individuals who meet theinclusion criteria and volunteer will be evaluated simultaneously by 3 expert physiotherapists on consecutive days (3 days) at the same time, with 3 repetitions using New York Posture Assessment.
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Posture Analysis with Static Observation (Lateral, Anterior, Posterior)
Time Frame: Individuals who meet the inclusion criteria and volunteer will be evaluated simultaneously by 3 expert physiotherapists on consecutive days (3 days) at the same time, with 3 repetitions using observational posture analysis
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Posture analysis performed with static observation is performed in 3 aspects: lateral posture analysis, anterior posture analysis and posterior posture analysis.
Observed disorders will be recorded by scoring between 0-3.
In the scoring system, 0 indicates no, 1 indicates mild, 2 indicates moderate and 3 indicates severe disorders.
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Individuals who meet the inclusion criteria and volunteer will be evaluated simultaneously by 3 expert physiotherapists on consecutive days (3 days) at the same time, with 3 repetitions using observational posture analysis
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Demographic Information Form
Time Frame: baseline
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With this form, information about the age, gender, height, weight, pregnancy status, educational status, occupation, smoking and alcohol use status, bag carrying style that may affect posture, frequency of computer use, study time, sports of interest and the duration of performing the sports of interest will be questioned.
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baseline
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Özlem Çinar Özdemir, Prof.Dr, Izmir Democracy University
Publications and helpful links
General Publications
- Fortin C, Feldman DE, Cheriet F, Labelle H. Clinical methods for quantifying body segment posture: a literature review. Disabil Rehabil. 2011;33(5):367-83. doi: 10.3109/09638288.2010.492066. Epub 2010 Jun 23.
- Czakwari A, Czernicki K, Durmala J. Faulty posture and style of life in young adults. Stud Health Technol Inform. 2008;140:107-10.
- Szucs KA, Brown EVD. Rater reliability and construct validity of a mobile application for posture analysis. J Phys Ther Sci. 2018 Jan;30(1):31-36. doi: 10.1589/jpts.30.31. Epub 2018 Jan 27.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- Izmir Democracy
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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