Overhead sport athletes, healthy volunteers Overhead sport athletes Overhead shoulder movement Shoulder ROM Validity of smartphone application Rotational movement Goniometer Dynamometer Inclinometer Visual estimation 3D motion analysis Opencap
Conditions
Interventions
Assessors are doctors who will stand in front of the participant. After participant perform shoulder movements, assessors will estimate the range of motion (ROM) of the motion as degrees.
,Assessors a
s cloud then it will process and calculate the detail of movement.,3D motion analysis is a method that captures and analyzes the movement of participant in three-dimensional space, using specialized s
Visual estimation,Standard goniometer,Dynamometer and inclinometer ,Mobile application (OpenCap),3 D motion analysis
Sponsors
Faculty of Medicine, Siriraj Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Professional or amateur athletes participating in overhead sports activities such as volleyball, badminton, tennis, baseball, or swimming, who have previously competed at district, provincial, or national levels 2. Age 18 - 40 years old 3. Absence of neurological disorders, musculoskeletal diseases, disability, or congenital abnormalities affecting the upper extremities, trunk, and spine 4. Ability to perform bilateral upper extremity and trunk movements 5. Ability to maintain stable standing position and lie supine flat on the ground 6. Ability to comprehend and follow procedural instructions 7. Availability to participate in the experimental study for a minimum duration of 2 hours
Exclusion criteria
Exclusion criteria: 1. Professional and amateur athletes currently experiencing shoulder injury with pain intensity exceeding 4 out of 10 on the numerical pain rating scale 2. Professional and amateur athletes with history of injury and/or disease affecting upper extremity and trunk function within 1 year 3. History of shoulder pathology on either side, including fractures, shoulder dislocation, neuromuscular abnormalities, non-traumatic pathological conditions, or previous surgical intervention in the shoulder region 4. Presence of chronic medical conditions or physical conditions precluding study participation 5. Experience of pain or numbness before initiation or during the conduct of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Accuracy of mobile application at the time assessed Results measured by mobile application compared with result measured by 3-D motion analysis | — |
Secondary
| Measure | Time frame |
|---|---|
| Differences of each devices at the time assessed Compare the differences of results measured by each devices | — |
Countries
Thailand
Contacts
Public ContactKrit Singthanuprasert
Faculty of Medicine, Siriraj Hospital, Mahidol University
Outcome results
None listed