Phase
Condition
N/ATreatment
Non-invasive EMG band instrumentation
Clinical Study ID
Ages > 21 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Individuals 21 years in age and older
Individuals with amputation of one or both arms at transradial level (applies toamputees only)
Ability to follow study directions
Willingness and ability to sign Informed Consent
Exclusion
Exclusion Criteria:
Individuals with previously diagnosed muscle pathologies
Individuals with impaired muscle function and/or impaired ability to perform normalhand movements (normal participants) or ability to perform normal phantom handmovements (amputees)
Individuals with transhumeral or higher amputation of both arms (applies to amputeesonly)
Cognitively impaired to follow study instructions
Allergies to skin adhesive materials necessary for cutaneous electrode placement
Excessive hair growth on arms and inability to shave off the hair for electrodeplacement
Pregnant woman
Arms or residual limbs with insufficient diameter to accommodate the wearing of twocutaneous sensor arrays
Injuries, bruises, or open wounds on the arm that needs to be instrumented for thestudy
Study Design
Study Description
Connect with a study center
Phantom Neuro Inc. Operational Headquarters
Austin, Texas 78704
United StatesActive - Recruiting
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