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Study of Medial-Lateral Center of Pressure Displacement in Unilateral Transfemoral Amputees

Investigation of Medial Lateral Displacement of Center of Pressure and Center of Mass During Double Support in Men With Unilateral Transfemoral Amputations.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02299674
Enrollment
3
Registered
2014-11-24
Start date
2014-11-30
Completion date
2017-05-31
Last updated
2017-05-03

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

Conditions

Unilateral Transfemoral Amputation

Brief summary

The purpose of this study is to examine the path and velocity of the center of mass (CoM) and center of pressure (CoP) during double support of persons walking with a unilateral above-the-knee prosthesis and determine the effects of prosthetic foot stiffness and effective length on CoM and CoP.Persons with a lower limb amputation walk with compensatory movements that affect the smooth trajectory of the center of mass (CoM) during weight transfer. The lack of control in the foot/ankle complex reduces fine motor movements, influencing the progression of the CoM and transfer of ground reaction forces represented by the center of pressure (CoP). Without control of the ankle joint, prosthetic users fall off of their trailing prosthetic limb during weight transfer, resulting in much more abrupt CoM and CoP transfers from trailing to leading limb. These abrupt movements during transfer not only increase stress on the sound limb, but also decrease the subject's energy efficiency during ambulation. The current study will further examine the CoP path and velocity in relation to the CoM path and velocity during double support of men with a transfemoral prosthesis, as well as explore how prosthetic foot ankle stiffness and effective length affects the CoP path and velocity.

Interventions

OTHERLevel overground ambulation

Sponsors

Southern California Institute for Research and Education
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Participants must have a transfermoral amputation and use an above-the-knee prosthesis with an articulating knee joint on a daily basis. * Participants must be male. * Age greater than or equal to 18 years, but less than 65 years. * Participants must have no known pathology or comorbidites that would affect their ambulatory ability * Ability to tolerate walking for a minimum of 100 yards over the course of a two and a half hour time period. * Ability to walk one block without needing to rest.

Exclusion criteria

* Use of ambulatory aids such as canes or crutches. * Any medical or psychosocial condition that, in the opinion of the investigator, could jeopardize the subject's participation, and compliance with the study criteria. * Bilateral amputations.

Design outcomes

Primary

MeasureTime frameDescription
Center of Pressure VelocityDouble Support Phase of Gait Cycle (2.5 hour)The Center of Pressure velocity in the X and Y direction \[cm/sec\] will be collected using a motion capture system and forceplates during a single session. This data will be collected during a single 2.5 hour data collection session. The time frame is specifically the Double Support phase of the gait cycle.

Countries

United States

Outcome results

None listed

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