- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03731507
KinectROM Application for Assessing Range of Motion in Upper and Lower Extremity: A Development and Validation Study (KinectROM)
July 27, 2020 updated by: Saime Nilay Arman
The aim of the study is to investigate the validity and reliability of KinectROM application for objectively evaluating range of motion (ROM)
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The application KinectROM called has been developed for assessing ROM with Kinect controller by our team.
So, shoulder, elbow, knee, hip and ankle ROM measurements will be made with universal goniometer and developed KinectROM application.
Study Type
Interventional
Enrollment (Actual)
45
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Istanbul, Turkey, 34740
- Istanbul University-Cerrahpasa
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-
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 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
inclusion Criteria: -Healthy individuals with 18-40 years
Exclusion Criteria:
-Have any limited extremity between the ages of 18-40 years.
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Range of motion in upper extremity
Assessment 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
|
A ROM measurement method called as KinectROM by us has been developed with Kinect Controller
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Range of Motion
Time Frame: baseline
|
ROM of shoulder, elbow, knee, hip and ankle will be made with universal goniometer and developed Kinect controller based measurement method.
|
baseline
|
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 (Actual)
November 5, 2018
Primary Completion (Actual)
November 30, 2018
Study Completion (Actual)
December 15, 2018
Study Registration Dates
First Submitted
November 3, 2018
First Submitted That Met QC Criteria
November 3, 2018
First Posted (Actual)
November 6, 2018
Study Record Updates
Last Update Posted (Actual)
July 29, 2020
Last Update Submitted That Met QC Criteria
July 27, 2020
Last Verified
July 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- IstanbulUC
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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