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NCT07779928 · ClinicalTrials.gov record · last posted 2026-08-21

An Innovative Proprioceptive Instrument for Upper Extremities

StatusNot Yet Recruiting
PhaseNot specified
Started2026-09-01
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from the ClinicalTrials.gov record
This study aimed to develop and validate an innovative proprioceptive assessment instrument for the upper extremities, the PropArm-PosiMoF (PropArm). This observational study was conducted in three stages. The first stage focused on the development and validation of PropArm, including test-retest reliability, concurrent validity, and convergent validity. The second stage established age norms and cut-off points in healthy adults. In the final stage, PropArm was applied to patients with proprioceptive impairments (stroke, shoulder impingement syndrome, and diabetes mellitus patients) to examine its diagnostic accuracy and clinical applicability.
Trial Details
NCT Number NCT07779928
Lead Sponsor National Cheng-Kung University Hospital
Conditions Stroke, Shoulder Impingement Syndrome, Diabetes (DM), Healthy Young Adults, Healthy Adults, Healthy Older Adults
Enrollment 280 participants
Start Date 2026-09-01
Primary Completion 2027-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-08-21