Effect of Socket Wall Height With Vacuum Suspension for Above Knee Amputees

Stony Brook University

Status and phase: Completed; Phase 1

Conditions: Amputation

Treatments: Device: Vacuum assisted socket technology (Harmony System, Otto Bock Healthcare)

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01559909

197622

Details and patient eligibility

About

Individuals with transfemoral (TF) amputation (above the knee amputation) may benefit from a socket that uses vacuum assisted suspension (VAS) to hold the socket onto the amputated limb. VAS may improve stability, weight bearing, comfort, proprioception, limb health, and function. To date, there is no evidence to support whether VAS alters balance, kinematics, and kinetics when walking for TF amputees as compared to conventional socket suspension technology. Further, there is question regarding what the optimal height of the socket should be to maintain stability and function. So long as stability is not sacrificed, it may be advantageous to lower the height of the socket to allow full hip motion and improve sitting comfort. The purpose of this investigation is to assess if the socket height alters the motion of the leg and changes the way one walks when using VAS compared to conventional socket suspension technology. In this study, TF amputees will be fitted with a VAS socket that will be attached to their current prosthesis using similar alignment. Individuals will be assessed while walking on a level floor and during stair negotiation while wearing the prosthesis with the VAS socket at various socket heights as well as their current socket. Additionally, balance and socket standing and sitting comfort will be investigated.

Enrollment: 10 estimated patients

Sex: All

Ages: 21 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or female between the ages of 21 and 75 with a transfemoral amputation.
• Limited household ambulators (K1) to those considered unlimited community ambulators (K4).
• People who are comfortably fitted with a prosthesis for at least 6 months.

Exclusion criteria

• People with severe cardiac or pulmonary disease that limits ability to walk.
• People with too much discomfort and/or pain.
• People with active wounds on their residual limb or other foot.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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10 participants in 1 patient group

Socket wall height

Experimental group

Treatment:

Device: Vacuum assisted socket technology (Harmony System, Otto Bock Healthcare)