KinectROM Application for Assessing Range of Motion in Upper and Lower Extremity: A Development and Validation Study
KinectROM
1 other identifier
interventional
45
1 country
1
Brief Summary
The aim of the study is to investigate the validity and reliability of KinectROM application for objectively evaluating range of motion (ROM)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2018
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 3, 2018
CompletedStudy Start
First participant enrolled
November 5, 2018
CompletedFirst Posted
Study publicly available on registry
November 6, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 30, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 15, 2018
CompletedJuly 29, 2020
July 1, 2020
25 days
November 3, 2018
July 27, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Range of Motion
ROM of shoulder, elbow, knee, hip and ankle will be made with universal goniometer and developed Kinect controller based measurement method.
baseline
Study Arms (1)
Range of motion in upper extremity
EXPERIMENTALAssessment of shoulder: flexion/extension, abduction/adduction, internal/external rotation, elbow flexion/extension, hip: flexion/extension, abduction/adduction, internal/external rotation, knee: flexion/extension, ankle: dorsal flexion/plantar flexion
Interventions
A ROM measurement method called as KinectROM by us has been developed with Kinect Controller
Eligibility Criteria
You may not qualify if:
- Have any limited extremity between the ages of 18-40 years.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul University-Cerrahpasa
Istanbul, 34740, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assist.Prof.
Study Record Dates
First Submitted
November 3, 2018
First Posted
November 6, 2018
Study Start
November 5, 2018
Primary Completion
November 30, 2018
Study Completion
December 15, 2018
Last Updated
July 29, 2020
Record last verified: 2020-07