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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03532100
Other study ID # A2456-R
Secondary ID RX002456 Part 1I
Status Recruiting
Phase N/A
First received
Last updated
Start date April 18, 2018
Est. completion date March 31, 2025

Study information

Verified date January 2024
Source VA Office of Research and Development
Contact Glenn K Klute, PhD
Phone (206) 764-2991
Email Glenn.Klute@va.gov
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

The human ankle is a complex mechanism that does not behave like a simple hinge. Instead, rotations in all three axes are allowed and some are coupled together. In particular, the axis of rotation of the talo-crural joint during ankle flexion is inclined downwards and laterally relative to horizontal, and the rotation ranges from 10 to 26 degrees among individuals. This rotation couples plantar- and dorsi-flexion motion with external and internal rotation of the shank relative to the foot, respectively. This feature of the natural limb has not been replicated in prosthetic feet and ankles. Lower limb amputees take thousands of steps on their prosthesis each day and none feature coupled motion between the transverse- and sagittal-planes. The absence of this natural coupling may be related to the high incidence of residual limb soft tissue injuries, the need for compensatory gait, and overall dissatisfaction with their prostheses. Transverse rotation adapters, consisting of simple torsional springs, are available for prescription. These devices can increase transverse-plane rotations and decrease transverse-plane torques, but their use is not widespread and if excessively compliant, may reduce gait stability. Cost, weight, prosthesis build height, and the inability for the user to adjust the stiffness may all play a role in their lack of adoption, but it may also be that the transverse-plane rotation is not coupled with the sagittal-plane. With these devices, motion only occurs in the transverse-plane when a transverse-plane torque is applied. 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 fit a sample population of unilateral transtibial amputees with the motor-driven and computer controlled torsionally adaptive prosthesis. Participants will walk in a straight line and in both directions around a circle with the torsionally adaptive prosthesis set at different coupling ratios (blinded and random order). The general hypotheses for this study are: (H1) a coupling ratio exists between 0 (no coupling) to 1:2 (one degree of transverse-plane motion for every two degrees of sagittal-plane motion) that minimizes transverse-plane socket torque and (H2) an amputee preferred coupling ratio will exist within this range. This research will discover how best to couple transverse- and sagittal-plane motion in the prostheses of lower limb amputees.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Torsionally adaptive prosthesis with 0:1 coupling ratio
The torsionally adaptive prosthesis can be programmed to couple the motion between the transverse- and sagittal-planes. A coupling ratio (transverse:sagittal) of 0:1 means there will be no coupling between the transverse- and sagittal-plane motion. That is, regardless of any motion in the sagittal plane, there will be zero motion in the transverse plane.
Torsionally adaptive prosthesis with 1:6 coupling ratio
The torsionally adaptive prosthesis can be programmed to couple the motion between the transverse- and sagittal-planes. A coupling ratio (transverse:sagittal) of 1:6 means there will be one degree of motion in the transverse plane for every six degrees of motion in the sagittal plane.
Torsionally adaptive prosthesis with 1:4 coupling ratio
The torsionally adaptive prosthesis can be programmed to couple the motion between the transverse- and sagittal-planes. A coupling ratio (transverse:sagittal) of 1:4 means there will be one degree of motion in the transverse plane for every four degrees of motion in the sagittal plane.
Torsionally adaptive prosthesis with 1:3 coupling ratio
The torsionally adaptive prosthesis can be programmed to couple the motion between the transverse- and sagittal-planes. A coupling ratio (transverse:sagittal) of 1:3 means there will be one degree of motion in the transverse plane for every three degrees of motion in the sagittal plane.
Torsionally adaptive prosthesis with 1:2 coupling ratio
The torsionally adaptive prosthesis can be programmed to couple the motion between the transverse- and sagittal-planes. A coupling ratio (transverse:sagittal) of 1:2 means there will be one degree of motion in the transverse plane for every two degrees of motion in the sagittal plane.

Locations

Country Name City State
United States VA Puget Sound Health Care System Seattle Division, Seattle, WA Seattle Washington

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

Outcome

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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