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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03731507
Other study ID # IstanbulUC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 5, 2018
Est. completion date December 15, 2018

Study information

Verified date July 2020
Source Istanbul University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to investigate the validity and reliability of KinectROM application for objectively evaluating range of motion (ROM)


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.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date December 15, 2018
Est. primary completion date November 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility inclusion Criteria: -Healthy individuals with 18-40 years

Exclusion Criteria:

-Have any limited extremity between the ages of 18-40 years.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Assessment of Range of Motion with Kinect Controller
A ROM measurement method called as KinectROM by us has been developed with Kinect Controller

Locations

Country Name City State
Turkey Istanbul University-Cerrahpasa Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Saime Nilay Arman

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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
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