Background
There exists a need for an adjustable socket to accommodate residual limb volume and shape changes. Further, limb loss rates globally are rising and there is a large unmet need for affordable and accessible prosthetic systems.
Objective
To assess the utility of an immediate fit modular prosthetic system (iFIT Prosthetics, LLC).
Design
Prospective feasibility study involving a 2âweek singleâgroup preâpost intervention study.
Setting
Physical Medicine and Rehabilitation gait laboratory.
Participants
Participants were at least 6 months post amputation and walking with a conventional prosthesis. They were free of skin wounds, other neurological disorders, and severe pain conditions.
Methods
Participants were fit with an immediate fit prosthesis and instructed to wear it for a 2âweek evaluation period. They were given a progressive wearing schedule and they completed outcome measurements at the 2âweek followâup.
Main Outcome Measurements
Selfâreported satisfaction, gait biomechanics, and intrasocket peak pressures.
Results
Twentyâsix participants entered the study, with 22 completing the single group preâpost study. They averaged 50âyears (SD ±10.2) of age; four were female. Sixteen were dysvascular and 10 were traumatic in etiology. Significant differences (Pâ=â.03) in selfâreported satisfaction were found in favor of the iFIT device 29.33 (SDâ±â4.51) versus the conventional device 25.52 (SDâ±â6.8). No falls or limb ischemia were reported. Gait biomechanics revealed no differences across any temporal characteristics. Intrasocket peak pressures were significantly lower for the iFIT prostheses overall (Pâ=â.0014), at the anterior tibia (Pâ=â.0002), and the lateral side of the residual limb (Pâ=â.013).
Conclusions
The iFIT transtibial prosthetic system appears to be safe in this shortâterm singleâgroup preâpost study. This study provided preliminary evidence to support the feasibility of the iFIT system. It compared favorably to participants' conventional prostheses across all outcome measures. With its cost, adjustability, and accessibility advantages, this device may prove useful for persons with transtibial amputations. A larger multicenter study is needed to confirm these results.
Level of Evidence
III