- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06504212
Validity and Reliability of a New Mobile Application
July 10, 2024 updated by: Gülfem Ezgi ÖZALTIN, Inonu University
Reliability and Validity Of A Mobile Applicatıon in the Evaluation of Elbow Joint Position Sense
In this study, we aimed to study the validity and reliability of the Angle Meter, a Smartphone application for elbow joint position sense.
Study Overview
Detailed Description
The validity and reliability of the elbow joint position sense with the mobile application will be evaluated with the angle meter.
This application works on phones with the IOS operating system.
The validity and reliability of the Angle Meter will be evaluated by comparing it with a small universal goniometer for measuring elbow range of motion.
The elbows of healthy subjects will be photographed at 3 different angles in the open and kinetic chain position.
The elbow photo of healthy individuals measured with the Angle meter will be evaluated simultaneously but independently with the Angle meter by 2 different evaluators.
The measurements will be repeated after 3 days.
It will be noted that each picture is sufficient, i.e. there is no obvious perspective error.
Study Type
Observational
Enrollment (Estimated)
4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: gulfem ezgi phd ozaltin, phd
- Phone Number: 05530285628
- Email: gulfemezgi.ozaltin@inonu.edu.tr
Study Contact Backup
- Name: dilan demirtas karaoba, Phd
- Phone Number: 05541127796
- Email: dilandemirtas92@gmail.com
Study Locations
-
-
Inonu University
-
Malatya, Inonu University, Turkey, 11000
- Recruiting
- Gulfem Ezgi
-
Contact:
- gulfem ezgi ozaltin, phd
- Phone Number: 05530285628
- Email: mailto:gulfemezgi.ozaltin@inonu.edu.tr
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
healthy individuals
Description
Inclusion Criteria:
- Being between the ages of 18-25
- Being healthy
- Agreeing to participate in the study
Exclusion Criteria:
- Those who have had upper extremity surgery within the last year
- Those with neurological, orthopedic, rheumatic or cardiovascular problems affecting the neck, shoulder, elbow, hand and wrist
- Those with central and peripheral nervous system involvement Having pain anywhere in the body
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
universal goniometer
Time Frame: [Time Frame: 3 days]
|
Joint position sense measurement with universal goniometer .
|
[Time Frame: 3 days]
|
|
mobile application
Time Frame: [Time Frame: 3 days]
|
The elbows will be photographed in 3 different angles, in open and kinetic chain position.
The elbow photograph of healthy individuals measured with the Angle meter will be evaluated simultaneously but independently with the Angle meter by 2 different evaluators.
|
[Time Frame: 3 days]
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: havva adli, Inonu University
- Study Chair: burcu talu, Inonu University
- Study Chair: dilan demirtas karaoba, Inonu University
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 (Estimated)
July 12, 2024
Primary Completion (Estimated)
October 12, 2024
Study Completion (Estimated)
November 12, 2024
Study Registration Dates
First Submitted
July 10, 2024
First Submitted That Met QC Criteria
July 10, 2024
First Posted (Actual)
July 16, 2024
Study Record Updates
Last Update Posted (Actual)
July 16, 2024
Last Update Submitted That Met QC Criteria
July 10, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2024/5554(2)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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