Clinical Trial

Comparison of Standard Myoelectric Hand and Bionic Hand Use in Individuals With Upper Limb Amputation

Completed
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Summary
This single-center, prospective, comparative study aims to compare hand function, quality of life, patient satisfaction, task completion time, fatigue, and compensatory elbow, shoulder, and cervical movements in individuals with transradial amputation or wrist disarticulation who use either standard myoelectric or bionic hand prostheses. The primary research questions are: 1. Are there differences in patient satisfaction, quality of life, and hand function between individuals using standard myoelectric and bionic hand prostheses? 2. Do individuals using standard myoelectric and bionic hand prostheses exhibit different kinematics in terms of compensatory shoulder, elbow, and neck movements? Could bionic hand prostheses with their diverse grasping capabilities lead to fewer compensatory movements compared to standard myoelectric hand prostheses? 3. Can fatigue induced by performing specific activities of daily living alter hand function and upper extremity-neck kinematics in individuals using either standard myoelectric or bionic hand prostheses? 4. Can cognitive and physical fatigue following activities of daily living lead to different levels of changes in hand function and upper extremity-neck kinematics in individuals using standard myoelectric and bionic hand prostheses?
Protocol Amendment History 2 changes
critical Trial completed 2026-07-21
minor Completion pushed: 2026-04-29 -> 2026-06-01 2026-07-21
Trial Details
NCT Number NCT06684730
Lead Sponsor Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Conditions Transradial Amputation, Wrist Disarticulation
Enrollment 22 participants
Start Date 2024-08-10
Primary Completion 2026-02-28 (estimated)
Study Completion 2026-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-20