Home › NCT07075042
Comparing the Attentional Demands and Functional Outcomes in People With Transradial Amputation
Comparing the Attentional Demands and Functional Outcomes of Pattern Recognition and Direct Myoelectric Control in People With Transradial Amputation
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * 18 years of age or older * Unilateral transradial limb loss * At least 6 months since loss * Previous or current use of a myoelectric device for 3 months or longer * Use of a prosthesis at least 4 days each week * Ability to read, write, and understand English * Willingness to use each control strategy as primary device for 3 months each (6 months commitment total) Exclusion Criteria: * Any health condition that would prevent safely completing trial activities * Discontinued use of a myoelectric prosthesis due to non-financial reasons
About the study
Different ways of controlling an upper-limb prosthesis can affect how easy it is to use and how helpful it is in everyday activities. One common method, called direct control, uses signals from two muscles and can make switching between movements difficult. Another clinically available option, called pattern recognition control, uses signals from several muscles to better understand the user's intended movement and may feel more natural to use. This study compares these two control methods to see how they affect function for adults with below-the-elbow limb loss.
What is being tested
- Training with PRC (device)
- Training with DC (device)
- PRC Device use in community and home (device)
- DC Device use in community and home (device)
Sponsor: Virginia Commonwealth University · Participants: 32 · Started: Jul 2, 2026
Contact the study team
- Shane R. Wurdeman, PhD · Phone: 281-829-4746
- Bretta L. Fylstra, PhD · Phone: 512-994-6685
Official record on ClinicalTrials.gov — NCT07075042
Locations in the U.S.
| Texas | Hanger Inc., Austin |
| Virginia | Virginia Commonwealth University, Richmond |
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.