Evaluating User Satisfaction and Feasibility of a Remote Model for 3d Scanned and Printed Transtibial Prosthetic Sockets

NCT ID: NCT06361966

Last Updated: 2024-04-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-01-11
• Study Completion Date: 2023-01-09

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 question[s] 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 weeks.The 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 patient's preferred socket to prosthesis.

Conditions

Amputation; Prosthesis User

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Laminate socket

control intervention as standard treatment for transtibial amputees requiring a lower limb prosthesis

Group Type: ACTIVE_COMPARATOR

3d printed prosthetic socket

Intervention Type: DEVICE

3d printed prosthetic socket produced through multi-jet fusion (MJF)

3d printed socket

trial intervention for transtibial amputees requiring a lower limb prosthesis

Group Type: EXPERIMENTAL

3d printed prosthetic socket

Intervention Type: DEVICE

3d printed prosthetic socket produced through multi-jet fusion (MJF)

Interventions

3d printed prosthetic socket

3d printed prosthetic socket produced through multi-jet fusion (MJF)

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Unilateral transtibial amputation, current transtibial prosthetic users minimally capable of community ambulation (mobility grades K2 - K4) who have completed gait training, current users of a roll on elastomeric or silicone liner system, and aged 21 years old and above to be able to provide informed consent.

Exclusion Criteria

1. Functional status: patients with severe aphasia or neglect (inability to obey 1 step commands), communication disorders precluding understanding of instructions, cognitive impairment, dementia, untreated depression or psychiatric disorder.

2. Mobility status: patients who are non-community ambulators (mobility grade K1) or who have not completed gait training

3. Active limb conditions: uncontrolled lower limb volume fluctuations, severe stump varus or valgus deformities and/or lower limb contractures of over 10 degrees, or with local limb conditions which could be exacerbated by research interventions such as open wounds, ulcers, stump pain or stump wounds/ulcers, neuromas, active arthritis or joint or limb pain.

4. Reproductive age females should not be pregnant during the study.

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 99 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Prosfit Technologies JSC

UNKNOWN

Sponsor Role: collaborator

Centre for Allied Health and Pharmacy Excellence (CAPE)

UNKNOWN

Sponsor Role: collaborator

Tan Tock Seng Hospital

OTHER

Sponsor Role: lead

Responsible Party

Tabitha Quake

Principal Prosthetist/Orthotist

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Tabitha Quake

Role: PRINCIPAL_INVESTIGATOR

Tan Tock Seng Hospital

Locations

Tan Tock Seng Hospital

Singapore, , Singapore

Countries

Singapore

Other Identifiers

2021/00638

Identifier Type: -

Identifier Source: org_study_id