Inclinometer Reliability in Seated Shoulder Position Sense Assessment
Inclinometer Assessment of Seated Shoulder Position Sense: Intra- and Inter-Rater Reliability and Validity
Study Overview
Status
Status
Conditions
Conditions
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Contacts and Locations
Study Locations
-
-
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Istanbul, Turkey, 34000
- Liv hospital Vadistanbul
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-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthy participants aged 18-60 with no current or past shoulder injury, trauma, or pain.
Exclusion Criteria:
- Pain in the upper extremity or neck
- Limited range of motion in the upper extremity joints
- Any history of upper extremity, cervical, or cranial injury
- Regular involvement in a sport or occupation that requires frequent overhead shoulder movements
- Performing strenuous exercise within 24 hours prior to the assessment
- Consumption of alcohol and/or illicit substances within 24 hours prior to the assessment
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Position Sense
Time Frame: 1 day
|
This study is an observational, cross-sectional investigation conducted to evaluate shoulder joint position sense (JPS) in healthy volunteers. It aims to assess the reliability of JPS measurements performed in a seated position using a digital inclinometer. Experimental Procedure: In this study, shoulder joint position sense (JPS) measurements will be conducted in a seated position using a digital inclinometer. Test Protocol: Participants will be asked to reproduce three different shoulder flexion and abduction angles: Low range: 55° ± 5° Middle range: 90° ± 5° High range: 125° ± 5° Participants will also be asked to reproduce a 20° ± 5° shoulder internal rotation (IR) and external rotation (ER) angle in the horizontal plane. After raising their arm to a randomly determined angle and holding it for a few seconds, they will be instructed to return to the starting position. They will then be asked to reproduce the angle they remember. |
1 day
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: pmr specialist, Liv hospital Vadistanbul
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- FSM PRH schoulder
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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