Lower Extremity Amputation Clinical Trial
Official title:
Pivot-Flex Foot: Torsionally Adaptive Prosthesis for Individuals With Lower Limb Amputation
When prescribing a prosthetic foot, clinicians face a dizzying array of choices as more than 200 different prosthetic feet are available. While these conventional prosthetic feet primarily function in the sagittal plane, the intact foot and ankle comprise a complex set of joints that allow rotation in multiple planes of motion. Some of these motions are coupled, meaning rotation in one plane induces motion in another. One such coupling is between the sagittal and transverse planes. For every step, plantar- and dorsi-flexion motion in the sagittal plane is coupled with external and internal rotation of the shank relative to the foot in the transverse plane. There is no prosthetic foot available for prescription that mimics this natural coupling. To investigate the need for this coupling, the investigators have built a torsionally adaptive prosthesis where the coupling ratio between the transverse- and sagittal-planes can be independently controlled with a motor. This research has one specific aim: to identify the optimal coupling ratio between transverse- and sagittal-plane motions using a novel, torsionally adaptive prosthesis for individuals with lower limb amputation. The investigators will conduct a human subject experiment wearing the motor-driven and computer controlled torsionally adaptive prosthesis. Individuals with lower limb amputation will be asked to walk in a straight line and in both directions around a circle while the coupling ratio between transverse- and sagittal-plane motions is varied between trials. Participants will be blinded to the coupling ratio. The investigators hypothesize that: (1) a coupling ratio exists that minimizes undesirable transverse-plane socket torque and (2) there will be a coupling ratio that individuals with lower limb amputation prefer.
Status | Recruiting |
Enrollment | 15 |
Est. completion date | March 31, 2025 |
Est. primary completion date | October 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Unilateral transtibial amputation - Been fit with a prosthesis and used it for at least six months - Wear the prosthesis for four or more hours on an average day - Prescribed prosthesis can accommodate fitment of the study prosthetic components to be tested (determined at initial visit) Exclusion Criteria: - Improper fit and suspension with current prosthesis and one cannot be achieved with clinical resources (determined at initial visit) - Current skin irritation or injury on residual limb - Osteoarthritis, injury, or pain that interferes with walking ability - Currently incarcerated - Pregnant (determined via self-report) - Inadequate cognitive function or language proficiency to consent to participate |
Country | Name | City | State |
---|---|---|---|
United States | VA Puget Sound Health Care System Seattle Division, Seattle, WA | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Peak transverse-plane prosthetic socket torque | Peak transverse-plane prosthetic socket torque measured while walking | During walking trials for each coupling ratio | |
Secondary | Satisfaction with the prosthesis | An 11-point Likert scale will be used to record the subject's perception of satisfaction with the prosthesis after completing the trials for each coupling ratio. Participants will be asked to rate their satisfaction with the prosthesis on a 0 - 10 scale where 0 and 10 represent the least amount satisfaction and most amount of satisfaction imaginable, respectively. | Immediately following walking trials for each coupling ratio |
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