3D-Printed Prosthetic Socket Adapter for Clinical Simulation Use in Resource-Limited Environments

Abstract

Background Prosthetics and Orthotics (P&O) education in low-income nations faces significant challenges due to the prohibitive cost and limited availability of essential training materials, particularly prosthetic components like socket adapters. This scarcity directly impedes practical skill development, forcing a reliance on theoretical instruction.

Methodology A structured methodology integrating CAD modeling (Siemens NX12), Finite Element Analysis (FEA) using Siemens NX Nastran, and Fused Deposition Modeling (FDM) with PLA filament on a Creality Ender 3 printer was employed. FEA simulations guided design refinements.

Findings Physical prototype testing confirmed outstanding results. The adapter demonstrated dimensional accuracy with less than 0.1 mm deviation using a digital Vernier caliper, crucial for interoperability. Mechanical compression testing on an Instron 5944 UTM showed the prototype withstood a maximum load of 600 N before significant deformation, far exceeding simulation needs. Furthermore, fitting and compatibility tests confirmed a seamless and secure fit with standard transtibial prosthetic components. The final print quality was visually satisfactory with minimal post-processing.

Conclusion This work validates 3D printing as a highly effective, affordable, and reproducible solution for creating functional P&O training tools. Our findings offer a significant step towards democratizing access to practical prosthetic education globally, establishing a replicable framework for developing essential, locally manufactured training aids in various engineering and medical fields.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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