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临床试验/NCT07329738
NCT07329738进行中(未招募)不适用

A 3D-Printed Prosthesis Portable Station: The Vancouver Limbkit Project

University of British Columbia1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2023年7月17日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
8
试验地点
1
主要终点
Timed Up and Go Test (TUG)

研究概览

简要总结

The goal of this single-subject research design (clinical trial) is to assess the functionality of the 3D printed prostheses and to compare them to the existing prostheses in terms of mobility, balance, utility, and comfort. Participants who have a unilateral or bilateral transtibial amputation wear their existing prosthesis for roughly 3 weeks, followed by 3 weeks wearing a 3D printed prosthesis. The research assistants collect data throughout each period remotely, with the exception of one in-person visit to participants' homes to prepare the setting for the virtual evaluation sessions.

详细描述

Once a participant is recruited and consent is obtained, Phase (A) begins with the research assistants conducting one home visit with the participant. This visit sets up the performance-based outcome measures, provides instructions for performing the tests, explains how to complete the online surveys, and clarifies how to take the video recordings. The research assistants distribute the Sociodemographic and Clinical Characteristics questionnaire to the participant via the UBC Qualtrics platform.

During Phase (A), the participant wears their definitive prosthesis and is remotely evaluated up to three times per week for three weeks. At the end of Phase (A), the participant receives an online self-reported survey to measure the utility of using the definitive prosthesis.

The participant then attends their prosthetic clinic to have measurements and a scan of their residual limb taken for the 3D printed prosthesis. The prosthetists use the "Comb" mobile scanner application, and the scans of the participants are securely stored and de-identified to maintain the confidentiality of the participants' information through the HIPAA-compliant Comb portal. The research assistant prints the prosthesis, which includes implanting a thermal sensor into the prosthesis to monitor the wear time. The participant visits the prosthetic clinic a second time to have the 3D printed prosthesis fitted by the relevant prosthetist in the team. The prosthetist ensures the new prosthesis is properly fitted and appropriate for use before allowing the participant to go home with it.

In Phase (B), the participant uses the 3D-printed prosthesis for three weeks and conducts the same outcome measures. At the end of Phase (B), the participant receives an online self-reported survey to measure the utility of using the 3D printed prosthesis.

Participants drop off the 3D-printed prostheses at their prosthetic clinics at the end of the study. Then the RA collects all the 3D printed prostheses to keep them in a locked cabinet in the principal investigator's office at the University of British Columbia.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Device Feasibility
盲法
None

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • are adults 19+ years,
  • have a unilateral or bilateral transtibial amputation,
  • have an existing definitive prosthesis,
  • use their definitive prosthesis two or more consecutive hours per day,
  • have no wounds on the residual limb.

排除标准

  • are unable to adequately complete self-report measures or communicate well enough to participate in the end of project interview,
  • have bilateral upper extremity amputations,
  • have poorly controlled comorbidities (e.g., unstable diabetes, advanced heart problems)

研究组 & 干预措施

Single group (one arm only)

Other

Single-subject design (AB): therefore, each participant goes through two phases:

A= use regular prosthesis B= use 3D-printed prosthesis

干预措施: 3D printed prosthetic sockets (Device)

结局指标

主要结局

Timed Up and Go Test (TUG)

时间窗: Measurements are collected three times a week for three weeks (nine times) in phase A and three times a week for three weeks (nine times) in phase B.

Participants rise from a chair, walk three meters, turn around a cone, return to the chair, and sit; time is recorded from start (standing) to finish (sitting). The TUG score is the average of two timed trials.

次要结局

  • Four Square Step Test (FSST)(Measurements are collected three times a week for three weeks (nine times) in phase A and three times a week for three weeks (nine times) in phase B.)
  • Activities-Specific Balance Confidence Scale (ABC)(Measurements are collected three times a week for three weeks (nine times) in phase A and three times a week for three weeks (nine times) in phase B.)
  • Socket comfort was measured with the Socket Comfort Score (SCS)(Measurements are collected three times a week for three weeks (nine times) in phase A and three times a week for three weeks (nine times) in phase B.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

William C. Miller

Professor

University of British Columbia

研究点 (1)

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