Development, Validation, and Clinical Application of an Innovative Proprioceptive Instrument for Upper Extremities: PropArm-PosiMoF (PropArm)
Development, Validation, and Clinical Application of an Innovative Proprioceptive Instrument for Upper Extremities: PropArm-PosiMoF (PropArm)
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.
Healthy Young Adults:
Inclusion Criteria:
Exclusion Criteria:
Healthy Adults:
Inclusion Criteria:
Exclusion Criteria:
Healthy Older Adults:
Inclusion Criteria:
Exclusion Criteria:
Stroke:
Inclusion Criteria:
Exclusion Criteria:
Shoulder Impingement Syndrome:
Inclusion Criteria:
Exclusion Criteria:
Diabetes (DM):
Inclusion Criteria:
(1) Age between 20 and 89 years,
(2) Diagnosis of diabetes mellitus by a specialist physician, based on one of the following:
Diagnosis of diabetes is confirmed if any two of items (a-c) are met, or if any one of them remains positive on repeat testing; fulfillment of item (d) alone is also sufficient for diagnosis.
Exclusion Criteria: