Viewing Study NCT06361966



Ignite Creation Date: 2024-05-06 @ 8:24 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06361966
Status: COMPLETED
Last Update Posted: 2024-04-12
First Post: 2024-04-08

Brief Title: Evaluating User Satisfaction and Feasibility of a Remote Model for 3d Scanned and Printed Transtibial Prosthetic Sockets
Sponsor: Tan Tock Seng Hospital
Organization: Tan Tock Seng Hospital

Study Overview

Official Title: Evaluating User Satisfaction and Feasibility of a Remote-digital Model for 3d Scanning and Printing of Prosthetic Sockets for Patients With Transtibial Amputation A Preliminary Clinical Trial
Status: COMPLETED
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to investigate the repeatability of application of a fully remote method of manufacturing 3D printing of prosthetic sockets for transtibial amputees and determine user satisfaction of sockets produced through these methods The study also aims to evaluate the time and cost effectiveness of this production model

The main questions it aims to answer are

1 To determine the repeatability and user satisfaction with transtibial sockets produced using a remote-digital method as compared to conventional manufacturing methods
2 To determine if transtibial prosthetic users have greater prosthetic satisfaction scores across the 4 Prosthesis Evaluation Questionnaire PEQ subscales of Utility UT Appearance AP Sounds SO and Residual Limb Health RL with the 3D printed socket fabricated through the remote-digital method compared to the laminate socket made using the conventional method
3 To determine if transtibial prosthetic users experience greater socket comfort with the 3D printed socket compared to the laminate socket

Participants will receive a 3D printed socket trial intervention and a laminate socket control intervention and will use each socket for a period of 4 weeksThe order of socket use will be randomised At the end of each 4 week period participants will rate their comfort and satisfaction with the socket At the end of the trial participants will indicate their preferred socket which will be fitted to their prosthesis

Participants will attend 6 visits across a total duration of 11 weeks during the course of the study
Detailed Description: The visit schedule for the study is as follows

Visit 1 Week 0 Attain consent and initiate casting and scanning process for 1 laminate and 1 3D printed transtibial socket
Visit 2 Week 3 Fitting and adjustment of first prosthetic socket either 3D printed or laminate socket Subjects to rate comfort of first socket
Visit 3 Week 5 Follow-up on any required device adjustments troubleshooting to first socket
Visit 4 Week 7 Evaluation of user satisfaction with first socket Subjects to fill up survey on first socket Fitting of other socket design second socket Subjects to rate comfort of second socket
Visit 5 Week 9 Follow-up on any required device adjustments troubleshooting to second socket
Visit 6 Week 11 Evaluation of user satisfaction with second socket Subjects to fill up survey on second socket and select their preferred socket Fitting of patients preferred socket to prosthesis

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None