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Effects of Pin and Vacuum Assisted Suspension Systems

A Comparison of the Effects of Pin and Vacuum Assisted Suspension Systems in Transtibial Amputees

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04155762
Enrollment
9
Registered
2019-11-07
Start date
2015-02-01
Completion date
2019-02-01
Last updated
2019-11-12

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

Conditions

Amputees, Artificial Limbs, Prosthesis User

Keywords

Amputees, Artificial Limbs, Prosthetic designs, Rehabilitation of prostheses users, Prosthetic suspension systems

Brief summary

This study was performed to determine the presence of any difference between Pin Suspension (PS) and Active Vacuum Suspension (AVS) on walking capacity, functional mobility, weight bearing in the prosthetic side, prosthetic satisfaction and body image were evaluated. Nine patients who don't have an obstacle to both socket applications in terms of stump height, type and edema were evaluated in this study. Both suspension systems were administered to the patients included in the study. First, amputees have used PS for 3 months following alignment of the prosthesis and training period. Then again they used AVS for 3 months following alignment of the prosthesis and training period. For each system, after adapting prosthesis 'LASAR posture' was used to evaluate weight bearing on the prosthetic side, '6 Minute Walk Test' for walking capacity, 'Time Up and Go' test for functional mobility, 'Prosthetic Satisfaction Index' for prosthetic satisfaction and 'Amputee Body Image Scale' for body. There were statistically significant difference between PS and AVS in terms of prosthetic side weight bearing percentage, walking capacity, functional mobility and prosthetic satisfaction (p\<0.05), in favor of AVS. There were not statistically significant difference between the body image scores (p\>0.05). From the view of function and prosthetic satisfaction, AVS was found to be more effective in transtibial amputees. It is believed that our study will be a guide to the future studies including higher number of amputees, different amputation levels and different suspension systems.

Interventions

OTHERPin Suspension System (a prosthetic suspension system)

Participants used the PSS for three months following fabrication and adjustment of the prosthesis, and a prosthetic training period.

OTHERVacuum-Assisted Suspension System (a prosthetic suspension system)

After PSS, participants employed the VASS for three months after a similar training period.

Sponsors

Hacettepe University
CollaboratorOTHER
Baskent University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Being able to walk without the use of any assistive device, * Having normal range of motion in the hip and knee at the amputated side.

Exclusion criteria

* Having any disadvantage about prosthetic device usage in terms of stump length, shape and edema, * Having movement limitation, * Having any discomfort or health problem (cardiopulmonary, neurological or orthopedic problems) that may affect gait other than amputation, * Having multiple extremity loss.

Design outcomes

Primary

MeasureTime frameDescription
Weight-bearing on the prosthetic side3 minutesThe percentage of total body weight borne on the amputated limb will be recorded.
Walking capacity6 minutesSix Minutes Walk Test will be used to assess walking capacity. Participants will walk for 6 minutes between two points which are 24 meters apart. The total meters walked during those 6 minutes will be recorded.
Functional mobility1 minuteThe Timed Up and Go Test will be used to assess functional mobility. The test starts from the seated position on the chair. With the onset of time, the participant leaves the chair, walks for 3 meters, turns 180 degrees, returns to the starting point, and sits in the chair back. The test is finished when the participant is returned to the initial position and the total time is recorded in seconds.
Prosthetic satisfaction5 minutesSatisfaction with Prosthesis Questionnaire (SAT-PRO) is a self-administered questionnaire for determining the participants' satisfaction with the use of the prosthesis. It consists of 15 items. For each item, participants mark the number that best describes their satisfaction with current prosthesis (3: totally agree, 2: rather agree, 1: rather disagree, 0: totally disagree). The items 6, 12 and 14 are scored in reverse. In total, lower scores indicate higher satisfaction; the maximum score that can be taken in the questionnaire is 45 points which means 100% satisfaction and 0 points means 0% satisfaction. The Turkish version of the SAT-PRO is a valid and reliable test that can be used to evaluate the prosthetic satisfaction of people with lower extremity amputation.
Body image perception5 minutesThe Amputee Body Image Scale (ABIS) is a self-administered questionnaire for determining how an amputee perceives and feels about his/her body experience. It consists of 20 items. The items 3, 12 and 16 are scored in reverse. The total score varies from 20 to 100; lower scores indicate better body image. The Turkish version of the ABIS was found to be valid and reliable.

Countries

Turkey (Türkiye)

Outcome results

None listed

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