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Optimizing Prosthetic and Bicycle Fit for Veterans With Transtibial Amputations

Optimizing Prosthetic and Bicycle Fit for Veterans With Transtibial Amputations

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03828331
Acronym
BestBikeFit
Enrollment
12
Registered
2019-02-04
Start date
2019-04-01
Completion date
2023-08-31
Last updated
2024-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amputation

Keywords

Rehabilitation

Brief summary

Bicycling is a promising form of low-impact exercise that could prevent/treat Type 2 diabetes. However, Veterans with transtibial amputations (TTAs) may not effectively utilize bicycling for rehabilitation and exercise due to improper bike fit, socket discomfort, and/or the potential for injury. An optimized prosthetic/bicycle fit could improve comfort and reduce injury risk by decreasing asymmetries between legs, lowering metabolic costs, and improving efficiency for Veterans with TTAs during bicycling. Moreover, the use of objective prosthetic/bicycle fit guidelines would allow clinicians to facilitate shorter appointment times and fewer revisits for Veterans with TTAs. The investigators will determine the physiological and biomechanical effects of different prosthetic and bicycle configurations for Veterans with a TTA to develop optimal prosthetic/bicycle fit guidelines. The investigators hypothesize that a longer prosthetic pylon length and shorter bicycle crank arm length for the affected compared to the unaffected leg along with a pedal attachment position beneath the pylon compared to beneath the forefoot will optimize performance for Veterans with TTAs the investigators' research will integrate evidence-based guidelines to advance rehabilitation and enhance the lives of Veterans with an amputation, thus improving and restoring their function.

Detailed description

Over one million people in the United States have a leg amputation and this number continues to grow due to the prevalence of diabetes and recent military conflicts. Because of the functional impairment caused by an amputation, it is extremely important to advance rehabilitation that optimizes the use of prostheses so that Veterans with amputations can regain the greatest possible level of health, function, and physical activity. Low-impact exercise such as bicycling could facilitate return to work/duty after amputation by improving cardiovascular fitness, muscle strength, endurance, and quality of life for Veterans with transtibial amputations (TTAs). Bicycling as exercise could also prevent the deleterious effects of vascular disease and diabetes by improving cardiovascular function, controlling body weight, decreasing the rate of re-amputation, and improving quality of life for Veterans with TTAs. However, it is likely that discomfort and the increased potential for secondary musculoskeletal injury due to the lack of a proper prosthetic/bike fit discourages Veterans with TTAs from using bicycling for rehabilitation and exercise. Moreover, it is unclear how prosthetic and bicycle components, such as pylon length (PL), pedal attachment position (PAP) beneath the prosthetic forefoot versus the pylon, and crank arm length (CAL) affect the biomechanics, metabolic costs, and comfort/ satisfaction of Veterans with TTAs. Thus, the investigators' goal is to challenge the state-of-the-science by developing evidence-based prosthetic and bicycle fit guidelines that optimize the biomechanics, metabolic costs, efficiency (mechanical power/metabolic power) and comfort/satisfaction for Veterans with TTAs. The Department of Veterans Affairs (VA) and Department of Defense (DoD) Rehabilitation Directive has put forth an initiative that aims to dramatically improve and restore function in wounded Veterans and Service members so that they have the choice to return to active duty or productive civilian employment. The proposed research will establish optimal prosthetic/bicycle fit guidelines, which would enhance function by improving cardiovascular health, controlling body weight, decreasing re-amputation rates, and enhancing quality of life of Veterans with TTAs, thus helping to fulfill this initiative and having high potential impact. Specifically, the investigators aim to: 1) Study 15 Veterans with unilateral TTAs to determine the effects of systematically varying PL, PAP beneath the prosthetic forefoot versus the pylon, and CAL for the affected leg on bicycling biomechanics, metabolic costs, and comfort/satisfaction. 2) Synthesize and disseminate the investigators' findings into practical, evidence-based quantitative prosthetic/bicycle fit guidelines for Veterans with TTAs. The investigators hypothesize that a longer PL and shorter CAL for the affected compared to the unaffected leg along with a PAP beneath the pylon compared to beneath the forefoot will maximize mechanical power symmetry and reduce metabolic cost and muscle activity, and thus maximize efficiency and comfort/satisfaction during bicycling in Veterans with unilateral TTAs. The utilization of evidence-based prosthetic/bicycle fit guidelines that increase symmetry, improve comfort, reduce the risk of injury, decrease metabolic costs, and improve efficiency will directly benefit Veterans with TTAs by increasing their physical activity and function. Optimized prosthetic/bicycle fit guidelines will allow Veterans TTAs who were previously unable to comfortably ride a bicycle, as well as those currently riding a bicycle, to ride longer with less effort and discomfort, potentially leading to an improved quality of life. Moreover, the prosthetic/bicycle fit guidelines generated by this research will ensure that clinicians are able to fit Veterans with TTAs to bicycles more effectively, leading to shorter appointment times and fewer revisits due to enhanced function and reduced comorbidities.

Interventions

OTHERProsthetic/Bicycle Configuration

The investigators will measure the biomechanics (motion, forces, and muscle activity) and metabolic rates while subjects ride using an initial bike fit and three taller pylon lengths (PL) for the affected leg (AL) in increments of 6.8 mm using a pedal attachment position (PAP) beneath the prosthetic forefoot. Then, using the optimal (most efficient) PL, the investigators will measure the biomechanics and metabolic rates while subjects ride using three shorter crank arm lengths (CALs) for the AL in decrements of 6.8 mm using a PAP beneath the prosthetic forefoot. On Day 2, the investigators will repeat the protocol of Day 1, but have riders use a PAP beneath the pylon for their AL.

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* One amputation below the knee * At least 1 year of experience using a prosthesis * No current problems with the prosthesis or residual limb * At or above a K3 Medicare Functional Classification Level

Exclusion criteria

* Poor general health * Difficulty with mobility * Problems with balance or dizziness * Current serious musculoskeletal injury besides that associated with an amputation * Cardiovascular, pulmonary, or neurological disease or disorder

Design outcomes

Primary

MeasureTime frameDescription
Mechanical Crank Power OutputData were collected over 2 days per subjectThe investigators calculated crank power output (W/kg) from the product of pedal torque and velocity and normalized this to participant body mass while participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).
Net Metabolic PowerData were collected over 2 days per subjectThe investigators measured net metabolic power (W/kg) using an equation that considers rates of oxygen consumption and carbon dioxide production and normalized this to participant body mass while participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).
Perceived Comfort (Visual Analog Scale (VAS))Data were collected over 2 days per subjectThe investigators measured comfort with a questionnaire that has a range of 0-10 that indicates terrible to excellent, respectively, after participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).
Perceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))Data were collected over 2 days per subjectThe investigators measured satisfaction with a questionnaire that has a range of 0-10 that indicates extremely dissatisfied to extremely satisfied, respectively, after participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).

Countries

United States

Participant flow

Participants by arm

ArmCount
Participants With Transtibial Amputation
The investigators will recruit participants with unilateral transtibial amputations who are at or above a K3 Medicare functional classification level (MFCL), and 18-55 years old. A K3 MFCL means that a person has the ability or potential for ambulation with variable cadence. A person at K3 MFCL is a typical community ambulator who has the ability to traverse most environmental barriers and may have vocational, therapeutic or exercise activity that demands prosthetic use beyond simple locomotion. Prosthetic/Bicycle Configuration: The investigators will measure the biomechanics (motion, forces, and muscle activity) and metabolic rates while subjects ride using an initial bike fit and three taller pylon lengths (PL) for the affected leg (AL) in increments of 6.8 mm using a pedal attachment position (PAP) beneath the prosthetic forefoot. Then, using the optimal (most efficient) PL, the investigators will measure the biomechanics and metabolic rates while subjects ride using three shorter crank arm lengths (CALs) for the AL in decrements of 6.8 mm using a PAP beneath the prosthetic forefoot. On Day 2, the investigators will repeat the protocol of Day 1, but have riders use a PAP beneath the pylon for their AL.
12
Total12

Baseline characteristics

CharacteristicParticipants With Transtibial Amputation
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
12 Participants
Age, Continuous39.4 years
STANDARD_DEVIATION 8.7
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
12 Participants
Region of Enrollment
United States
12 Participants
Sex: Female, Male
Female
6 Participants
Sex: Female, Male
Male
6 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 12
other
Total, other adverse events
0 / 12
serious
Total, serious adverse events
0 / 12

Outcome results

Primary

Mechanical Crank Power Output

The investigators calculated crank power output (W/kg) from the product of pedal torque and velocity and normalized this to participant body mass while participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).

Time frame: Data were collected over 2 days per subject

ArmMeasureValue (MEAN)Dispersion
CSP, AL, 160mm CAL, 0 mm PLMechanical Crank Power Output0.59 W/kgStandard Deviation 0.04
CSP, UL, 160mm CAL, 0 mm PLMechanical Crank Power Output0.99 W/kgStandard Deviation 0.03
CSP, AL, 165mm CAL, 0 mm PLMechanical Crank Power Output0.60 W/kgStandard Deviation 0.04
CSP, UL, 165mm CAL, 0 mm PLMechanical Crank Power Output0.97 W/kgStandard Deviation 0.03
CSP, AL, 170mm CAL, 0 mm PLMechanical Crank Power Output0.59 W/kgStandard Deviation 0.04
CSP, UL, 170mm CAL, 0 mm PLMechanical Crank Power Output0.95 W/kgStandard Deviation 0.03
CSP, AL, 175mm CAL, 0 mm PLMechanical Crank Power Output0.60 W/kgStandard Deviation 0.05
CSP, UL, 175mm CAL, 0 mm PLMechanical Crank Power Output0.95 W/kgStandard Deviation 0.03
CSP, AL, 175mm CAL, 5 mm PLMechanical Crank Power Output0.58 W/kgStandard Deviation 0.04
CSP, UL, 175mm CAL, 5 mm PLMechanical Crank Power Output0.98 W/kgStandard Deviation 0.03
CSP, AL, 175mm CAL, 10 mm PLMechanical Crank Power Output0.58 W/kgStandard Deviation 0.04
CSP, UL, 175mm CAL, 10 mm PLMechanical Crank Power Output0.98 W/kgStandard Deviation 0.03
CSP, AL, 175mm CAL, 15 mm PLMechanical Crank Power Output0.57 W/kgStandard Deviation 0.04
CSP, UL, 175mm CAL, 15 mm PLMechanical Crank Power Output0.99 W/kgStandard Deviation 0.04
DU, AL, 160mm CAL, 0 mm PLMechanical Crank Power Output0.56 W/kgStandard Deviation 0.04
DU, UL, 160mm CAL, 0 mm PLMechanical Crank Power Output0.98 W/kgStandard Deviation 0.03
DU, AL, 165mm CAL, 0 mm PLMechanical Crank Power Output0.56 W/kgStandard Deviation 0.04
DU, UL, 165mm CAL, 0 mm PLMechanical Crank Power Output0.99 W/kgStandard Deviation 0.03
DU, AL, 170mm CAL, 0 mm PLMechanical Crank Power Output0.56 W/kgStandard Deviation 0.04
DU, UL, 170mm CAL, 0 mm PLMechanical Crank Power Output0.96 W/kgStandard Deviation 0.03
DU, AL, 175mm CAL, 0 mm PLMechanical Crank Power Output0.57 W/kgStandard Deviation 0.04
DU, UL, 175mm CAL, 0 mm PLMechanical Crank Power Output0.97 W/kgStandard Deviation 0.03
DU, AL, 175mm CAL, 5 mm PLMechanical Crank Power Output0.58 W/kgStandard Deviation 0.04
DU, UL, 175mm CAL, 5 mm PLMechanical Crank Power Output0.94 W/kgStandard Deviation 0.03
DU, AL, 175mm CAL, 10 mm PLMechanical Crank Power Output0.56 W/kgStandard Deviation 0.04
DU, UL, 175mm CAL, 10 mm PLMechanical Crank Power Output0.96 W/kgStandard Deviation 0.03
DU, AL, 175mm CAL, 15 mm PLMechanical Crank Power Output0.55 W/kgStandard Deviation 0.05
DU, UL, 175mm CAL, 15 mm PLMechanical Crank Power Output0.99 W/kgStandard Deviation 0.03
Primary

Net Metabolic Power

The investigators measured net metabolic power (W/kg) using an equation that considers rates of oxygen consumption and carbon dioxide production and normalized this to participant body mass while participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).

Time frame: Data were collected over 2 days per subject

ArmMeasureValue (MEAN)Dispersion
CSP, AL, 160mm CAL, 0 mm PLNet Metabolic Power7.06 W/kgStandard Deviation 0.29
CSP, UL, 160mm CAL, 0 mm PLNet Metabolic Power7.18 W/kgStandard Deviation 0.3
CSP, AL, 165mm CAL, 0 mm PLNet Metabolic Power7.09 W/kgStandard Deviation 0.28
CSP, UL, 165mm CAL, 0 mm PLNet Metabolic Power6.94 W/kgStandard Deviation 0.28
CSP, AL, 170mm CAL, 0 mm PLNet Metabolic Power7.13 W/kgStandard Deviation 0.3
CSP, UL, 170mm CAL, 0 mm PLNet Metabolic Power7.14 W/kgStandard Deviation 0.31
CSP, AL, 175mm CAL, 0 mm PLNet Metabolic Power7.16 W/kgStandard Deviation 0.27
CSP, UL, 175mm CAL, 0 mm PLNet Metabolic Power7.18 W/kgStandard Deviation 0.28
CSP, AL, 175mm CAL, 5 mm PLNet Metabolic Power7.19 W/kgStandard Deviation 0.25
CSP, UL, 175mm CAL, 5 mm PLNet Metabolic Power7.23 W/kgStandard Deviation 0.29
CSP, AL, 175mm CAL, 10 mm PLNet Metabolic Power7.20 W/kgStandard Deviation 0.27
CSP, UL, 175mm CAL, 10 mm PLNet Metabolic Power6.74 W/kgStandard Deviation 0.66
CSP, AL, 175mm CAL, 15 mm PLNet Metabolic Power7.30 W/kgStandard Deviation 0.26
CSP, UL, 175mm CAL, 15 mm PLNet Metabolic Power7.37 W/kgStandard Deviation 0.28
Primary

Perceived Comfort (Visual Analog Scale (VAS))

The investigators measured comfort with a questionnaire that has a range of 0-10 that indicates terrible to excellent, respectively, after participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).

Time frame: Data were collected over 2 days per subject

ArmMeasureValue (MEAN)Dispersion
CSP, AL, 160mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.25 score on a scale of 0-10Standard Deviation 1.42
CSP, UL, 160mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.08 score on a scale of 0-10Standard Deviation 1.56
CSP, AL, 165mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.08 score on a scale of 0-10Standard Deviation 1.62
CSP, UL, 165mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.17 score on a scale of 0-10Standard Deviation 1.53
CSP, AL, 170mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.17 score on a scale of 0-10Standard Deviation 1.47
CSP, UL, 170mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.17 score on a scale of 0-10Standard Deviation 1.47
CSP, AL, 175mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))7.64 score on a scale of 0-10Standard Deviation 1.57
CSP, UL, 175mm CAL, 0 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.42 score on a scale of 0-10Standard Deviation 1.56
CSP, AL, 175mm CAL, 5 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.08 score on a scale of 0-10Standard Deviation 1.78
CSP, UL, 175mm CAL, 5 mm PLPerceived Comfort (Visual Analog Scale (VAS))8.08 score on a scale of 0-10Standard Deviation 2.15
CSP, AL, 175mm CAL, 10 mm PLPerceived Comfort (Visual Analog Scale (VAS))7.67 score on a scale of 0-10Standard Deviation 2.81
CSP, UL, 175mm CAL, 10 mm PLPerceived Comfort (Visual Analog Scale (VAS))7.67 score on a scale of 0-10Standard Deviation 2.67
CSP, AL, 175mm CAL, 15 mm PLPerceived Comfort (Visual Analog Scale (VAS))7.50 score on a scale of 0-10Standard Deviation 1.73
CSP, UL, 175mm CAL, 15 mm PLPerceived Comfort (Visual Analog Scale (VAS))7.00 score on a scale of 0-10Standard Deviation 1.9
Primary

Perceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))

The investigators measured satisfaction with a questionnaire that has a range of 0-10 that indicates extremely dissatisfied to extremely satisfied, respectively, after participants rode at 1.5 W/kg using different prosthetic and bicycle configurations (pylon length, crank arm length, and pedal attachment position).

Time frame: Data were collected over 2 days per subject

ArmMeasureValue (MEAN)Dispersion
CSP, AL, 160mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.58 score on a scale of 0-10Standard Deviation 2.53
CSP, UL, 160mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.33 score on a scale of 0-10Standard Deviation 2.64
CSP, AL, 165mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.17 score on a scale of 0-10Standard Deviation 2.69
CSP, UL, 165mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.58 score on a scale of 0-10Standard Deviation 2.84
CSP, AL, 170mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.50 score on a scale of 0-10Standard Deviation 2.68
CSP, UL, 170mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.33 score on a scale of 0-10Standard Deviation 2.84
CSP, AL, 175mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))6.64 score on a scale of 0-10Standard Deviation 2.84
CSP, UL, 175mm CAL, 0 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.83 score on a scale of 0-10Standard Deviation 1.85
CSP, AL, 175mm CAL, 5 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.75 score on a scale of 0-10Standard Deviation 2.3
CSP, UL, 175mm CAL, 5 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.58 score on a scale of 0-10Standard Deviation 2.57
CSP, AL, 175mm CAL, 10 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.25 score on a scale of 0-10Standard Deviation 2.6
CSP, UL, 175mm CAL, 10 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.42 score on a scale of 0-10Standard Deviation 2.54
CSP, AL, 175mm CAL, 15 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))7.00 score on a scale of 0-10Standard Deviation 2.45
CSP, UL, 175mm CAL, 15 mm PLPerceived Satisfaction (Prosthesis Evaluation Questionnaire (PEQ))6.00 score on a scale of 0-10Standard Deviation 2.72

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026