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NCT07779928

An Innovative Proprioceptive Instrument for Upper Extremities

Sponsor: National Cheng-Kung University Hospital

View on ClinicalTrials.gov

Summary

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.

Official title: Development, Validation, and Clinical Application of an Innovative Proprioceptive Instrument for Upper Extremities: PropArm-PosiMoF (PropArm)

Key Details

Gender

All

Age Range

20 Years - 89 Years

Study Type

OBSERVATIONAL

Enrollment

280

Start Date

2026-09-01

Completion Date

2027-12-31

Last Updated

2026-08-21

Healthy Volunteers

Yes