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Clinical Trials/NCT07298629
NCT07298629
Recruiting
Not Applicable

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

National Taiwan University Hospital1 site in 1 country30 target enrollmentStarted: July 1, 2024Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
30
Locations
1
Primary Endpoint
Foot pressure

Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Foot pressure

Time Frame: Baseline, Week 1, Week 4

Foot functional Index

Time Frame: Baseline, Week 1, Week 4

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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