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临床试验/NCT07298629
NCT07298629招募中不适用

Product Information Analysis and Clinical Verification - Clinical Verification of New Smart Health Medical Shoes/Insoles

National Taiwan University Hospital2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年7月1日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
2
主要终点
Foot pressure

研究概览

简要总结

As part of foot orthotics, insoles play a crucial role in adjusting biomechanical malalignments of the foot and regulating foot pressure. They are commonly used as a clinical tool for correcting foot problems. Currently, most customized insole manufacturing processes mainly depend on traditional or subtractive methods, highly dependent on the manual technology of the manufacturer, and the production capacity is constrained by working hours and cannot be manufactured in large quantities. Consequently, people often need to wait for one to two months with poor timeliness. The 3D printing insole fabrication process offers significant advantages in customization with high design flexibility and freedom. Utilizing microstructural zoning designs can better combine different regional characteristic requirements, thus closely addressing individual requirements. The purpose of this project is to validate the medical process after the initial development of the novel intelligent health medical insole and subsequently introduce the new intelligent health medical insole into clinical applications within medical institutions.

The project plans to recruit 30 participants with foot pain. Participants will be required to provide basic information and evaluated their foot condition. the Tiger Scan 3D full-foot scanning equipment will be used to capture the participants' 3D foot models. Insoles will be customized based on the assessment results, incorporating features such as heel cups, arch supports, and medial wedges. Relevant parameters will be uploaded to a RESTful API correction information platform. Then, the clinical recommendations for adjustment parameters will be output to a 3D printer, producing customized insoles with selective laser sintering (SLS) technology. The outcome assessments encompass short-term and long-term evaluations. Short-term assessments include kinematics and dynamic analysis, foot pressure distribution, physical performance, and foot morphology. Long-term assessments include pain levels, activities of daily living, and changes in quality of life.

研究设计

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

入排标准

年龄范围
20 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Obvious medial arch collapse
  • Foot posture index (FPI) score of 6 or higher

排除标准

  • experience wearing custom-made insoles within the past 6 months;
  • experience of lower limb injury, surgery, acute infection, or other complications within the past 6 months
  • a body mass index (BMI) greater than 35;
  • rheumatoid arthritis;
  • cognitive impairment preventing obedience;
  • systemic diseases affecting the nervous, muscular, skeletal, or circulatory systems

结局指标

主要结局

Foot pressure

时间窗: Baseline, Week 1, Week 4

Foot functional Index

时间窗: Baseline, Week 1, Week 4

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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