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

Launched by GAZILER PHYSICAL MEDICINE AND REHABILITATION EDUCATION AND RESEARCH HOSPITAL · Nov 9, 2024

Keywords

ClinConnect Summary

This clinical trial is studying how two types of hand prostheses—standard myoelectric hands and bionic hands—affect the daily lives of individuals with transradial amputation (below the elbow) or wrist disarticulation. Researchers want to find out if there are differences in how satisfied users feel, their quality of life, and how well they can use their hands. They will also look at how much energy is used when performing daily tasks and whether using bionic hands leads to less strain on the shoulders, elbows, and neck compared to standard myoelectric hands.

To participate in this study, you need to be between 18 and 65 years old and have had a transradial amputation or wrist disarticulation for at least six months. It’s important that you do not have any other conditions that could affect the results, such as neurological disorders or significant upper body issues. If you join the study, you will be asked to complete various tasks and provide feedback about your experiences with the prostheses. This research aims to help improve prosthetic design and user experience, making life easier for individuals with limb loss.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Having a transradial amputation or wrist disarticulation due to acquired or congenital causes,
• • Using a standard myoelectric or bionic hand prosthesis for at least 6 months,
• • Being between the ages of 18 and 65,
• • Having no neurological or cognitive disorders, rheumatic diseases, or other upper extremity dysfunction that could affect test results, and
• • Having signed an informed consent form indicating the patient's willingness to participate in the study.
• Exclusion Criteria:
• • Individuals younger than 18 or older than 65,
• • Those with additional musculoskeletal or neurological conditions preventing them from completing the tests and scales,
• • Those with psychiatric disorders or cognitive impairments preventing them from completing the questionnaire and assessment scales,
• • Those with stump or upper extremity conditions preventing them from using their prosthesis.