Comparing standard myoelectric and bionic hands for upper limb amputees
Comparison of Standard Myoelectric Hand and Bionic Hand Use in Individuals With Upper Limb Amputation
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital · NCT06684730
This study is testing whether standard myoelectric hands or bionic hands work better for people with arm amputations in terms of daily activities and overall satisfaction.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 22 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Gaziler Physical Medicine and Rehabilitation Education and Research Hospital (other) |
| Locations | 1 site (Ankara, ÇANKAYA) |
| Trial ID | NCT06684730 on ClinicalTrials.gov |
What this trial studies
This observational study compares the effectiveness of standard myoelectric hands and bionic hands in individuals with transradial amputation or wrist disarticulation. It evaluates hand function, quality of life, patient satisfaction, task completion time, fatigue, and compensatory movements in the upper body. Participants will be assessed using various scales and kinematic analysis to determine differences in performance and satisfaction between the two types of prostheses. The study aims to provide insights into how different prosthetic designs impact daily living activities and overall well-being.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18 to 65 with transradial amputation or wrist disarticulation who have been using either a standard myoelectric or bionic hand prosthesis for at least six months.
Not a fit: Patients with additional musculoskeletal or neurological conditions, cognitive impairments, or those outside the age range of 18 to 65 may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved prosthetic options that enhance the quality of life and functional capabilities for upper limb amputees.
How similar studies have performed: While there have been studies comparing different types of prostheses, this specific comparative approach between standard myoelectric and bionic hands is relatively novel.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
Ankara, ÇANKAYA
- Gaziler Physical Therapy and Rehabilitation Training and Research Hospital — Ankara, ÇANKAYA, Turkey (Türkiye) (RECRUITING)
Study contacts
- Study coordinator: Nurdan KORKMAZ, MD
- Email: nurizkorkmaz@hotmail.com
- Phone: +903122912410
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Transradial Amputation, Wrist Disarticulation, Standard Myoelectric Hand, Bionic Hand, Wrist disarticulation, Amputation of upper limb