Validity and Reliability of Dr. Goniometer in Elbow Flexion
ConditionElbow Joint Injuries
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorUniversity of Beykent
About this trial
This study aims to evaluate the validity and reliability of the Dr. Goniometer application for measuring elbow flexion by comparing it with a manual goniometer. Conducted at Beykent University, the study will include 60 participants without upper extremity issues. Measurements will be taken on the dominant arm using both a manual goniometer and Dr. Goniometer, each repeated twice. Dr. Goniometer measurements will be performed twice by two different evaluators. Validity will be assessed using the Pearson correlation coefficient, while reliability will be evaluated with ICC and SEM. Measurement differences will be analyzed using a paired t-test. The results will contribute to determining the clinical applicability of the Dr. Goniometer application.
Eligibility criteria
Qualifiers
Aged between 18 and 65 years
No history of musculoskeletal, neurological, or orthopedic conditions
Voluntary participation
Disqualifiers
History of musculoskeletal, neurological, or orthopedic disorders affecting the upper extremity.
Previous upper extremity trauma, surgery, or chronic pain limiting range of motion.
Inability to provide informed consent or follow verbal instructions.
Trial design
Treatments tested in this trial
- Dr. Goniometer Application
Treatment groups
60 Participants
are divided into 1 treatment groupLocations
Sponsors and collaborators
Source ClinicalTrials.gov