Evaluating a wireless control system for upper limb prostheses
Wireless Non-Invasive Advanced Control of Microprocessor Prostheses and Orthoses II
This study is testing a new wireless control system for arm prosthetics to see if it makes users happier and gives them better control compared to regular prosthetic setups.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 5 (estimated) |
| Ages | 18 Years to 89 Years |
| Sex | All |
| Sponsor | Liberating Technologies, Inc. Industry-sponsored |
| Locations | 1 site (Holliston, Massachusetts) |
| Trial ID | NCT06821412 on ClinicalTrials.gov |
What this trial studies
This project aims to assess the effectiveness of the ASTERISK wireless electrode system for users of transradial prostheses. The study will compare user satisfaction with the ASTERISK system against standard prosthetic configurations using a randomized 2x2 crossover design. Participants will wear the ASTERISK system, which allows for wireless transmission of myoelectric signals, under a prosthetic liner, enhancing comfort and control. The findings will inform the development of this technology into a commercial product and contribute to future prosthetic designs.
Who should consider this trial
Good fit: Ideal candidates are individuals who currently use trans-radial myoelectric prostheses or orthoses and have done so for at least six months.
Not a fit: Patients with neurological or physical conditions that hinder their ability to perform experimental tasks may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve user satisfaction and control for individuals with upper limb amputations.
How similar studies have performed: While the approach of using wireless electrodes is innovative, similar studies have shown promise in enhancing prosthetic control and user satisfaction.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * current wearers of trans-radial myoelectric prostheses or orthoses * have used their prostheses/orthoses for at least six months * understand spoken and written English (for the purpose of consenting) Exclusion Criteria: * have any neurological or physical conditions which would prevent them from performing the experimental tasks * are pregnant
Where this trial is running
Holliston, Massachusetts
- Liberating Technologies, Inc. — Holliston, Massachusetts, United States (Recruiting)
Study contacts
- Principal investigator: Benjamin McDonald — Liberating Technologies, Inc.
- Study coordinator: Benjamin McDonald
- Email: benjamin.mcdonald@liberatingtech.com
- Phone: 508-893-6363
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.