Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
240 participants
OBSERVATIONAL
2021-09-01
2024-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
This study aims to investigate the correlation and agreement of using Kinect in estimating skeletal length and body composition in human.A total of 240 participants including children and adults will be recruited for measurements in a 3-year period.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Children and adult
Participants aged 6-65 years old are recruited for the measurements of depth camera, bioelectrical impedance analysis and dual energy X-ray absorptiometry.
Microsoft Azure Kinect Developer Kit
3D images and 3D joint coordinates are obtained.
Bioelectrical impedance analyzer
Fat mass, fat-free mass and percentage body fat in total body and body segments are estimated.
Dual Energy X-ray Absorptiometry
Skeletal length and body composition are estimated.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Microsoft Azure Kinect Developer Kit
3D images and 3D joint coordinates are obtained.
Bioelectrical impedance analyzer
Fat mass, fat-free mass and percentage body fat in total body and body segments are estimated.
Dual Energy X-ray Absorptiometry
Skeletal length and body composition are estimated.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Age 6-65 years
Exclusion Criteria
* Pregnant
* Metal implant(s) or splint(s)
* Pacemaker implantation
* Limb defect(s) or injury
6 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ministry of Science and Technology, Taiwan
OTHER_GOV
Chang Gung Memorial Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Li-Wen Lee
Consultant Radiologist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Li-Wen Lee, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Chang Gung Memorial Hospital, Chiayi, Taiwan
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chang Gung Memorial Hospital
Chiayi City, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Li-Wen Lee, MD, PhD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
202002212A3
Identifier Type: -
Identifier Source: org_study_id