The Effect of Customized Insoles on Biomechanics and Pain in Patients With Functional Flatfoot
Primary Purpose
Flexible Flatfoot
Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Insole
Sponsored by
About this trial
This is an interventional treatment trial for Flexible Flatfoot
Eligibility Criteria
Inclusion Criteria:
- Aged between 20 and 65 years old
- Appearance of decreased medial arch
- Foot posture index score between 6 to 12
Exclusion Criteria:
- History of injuries of the lower extremity within the past 6 months
- Experience of use of orthopedic insole within the past 6 months
- Acute disorders in the lower extremities and spine
- History of surgery on the lower extremities and lumbar spine within the past 6 months
Sites / Locations
- Physical therapy center, national Taiwan university hosipital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
customized insole group
Arm Description
Outcomes
Primary Outcome Measures
F-scan system
measure peak plantar pressure, contact area, peak force and center of pressure excursion index during walking and center of pressure velocity and center of pressure 95% ellipse area during one leg stance by F-scan system
Secondary Outcome Measures
Visual analogue scale
This scale is used to measure pain and wearing comfort during sitting, standing and walking. For pain measurement, the maximum value is 10, which means severe pain. The minimum value is 0, which means absence of pain. For comfort measurement, the maximum value is 10, which means most comfortable. The minimum value is 0, which means absence of comfort.
Foot function index
Foot function index is used to measure foot condition. It contains 23 items, which are divided into three subscales: activity limitation, disability, and pain.
The patient scores each question on a scale from 0 (no pain or difficulty) to 10 (worst pain imaginable or so difficult it requires help), that best describes their foot over the past week.
Higher scores indicates worse pain. Both total and subcategory scores are calculated.
Full Information
NCT ID
NCT04381039
First Posted
May 5, 2020
Last Updated
October 18, 2021
Sponsor
National Taiwan University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04381039
Brief Title
The Effect of Customized Insoles on Biomechanics and Pain in Patients With Functional Flatfoot
Official Title
The Effect of Customized Insoles on Biomechanics and Pain in Patients With Functional Flatfoot
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
August 1, 2020 (Actual)
Study Completion Date
August 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of present study is to compare the effects of 3D printing customized insoles using different thermoplastic materials on functional flatfoot patients' foot function and biomechanics
Detailed Description
Functional flatfoot is a common foot disease which induces pain and functional decline. Insoles can be used for intervention and correction, especially customized insoles which are made according to different foot types. There have been few studies using 3D printing for customized insoles for functional flatfoot. Besides, compared to traditional method and subtractive manufacturing, the effect of 3D printing customized insoles is still controversial and depends on technology, materials and design.The purpose of present study is to compare the effects of 3D printing customized insoles using different thermoplastic materials on functional flatfoot patients' foot function and biomechanics. Twelve patients with functional flatfoot (foot function index> 6) aged 20-65 years old will be recruited in this study. Participants plan to wear three kinds of customized insoles fabricated by 3D printing with Nylon and TPU or computer numerical control machine with EVA. F-Scan system and questionnaires will be used to record foot biomechanics and pain after wearing insoles immediately, and foot condition after three weeks. Statistical analysis will be adopted for repeated-measures analysis of variance (ANOVA) for all outcome measures and post-hoc test will be used to test the difference between groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Flexible Flatfoot
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
customized insole group
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Insole
Intervention Description
3D printing insole (Nylon), 3D printing insole (TPU), CNC machine insole (EVA), shoe only
Primary Outcome Measure Information:
Title
F-scan system
Description
measure peak plantar pressure, contact area, peak force and center of pressure excursion index during walking and center of pressure velocity and center of pressure 95% ellipse area during one leg stance by F-scan system
Time Frame
after wearing insole (immediate effect)
Secondary Outcome Measure Information:
Title
Visual analogue scale
Description
This scale is used to measure pain and wearing comfort during sitting, standing and walking. For pain measurement, the maximum value is 10, which means severe pain. The minimum value is 0, which means absence of pain. For comfort measurement, the maximum value is 10, which means most comfortable. The minimum value is 0, which means absence of comfort.
Time Frame
after wearing insole (immediate effect)
Title
Foot function index
Description
Foot function index is used to measure foot condition. It contains 23 items, which are divided into three subscales: activity limitation, disability, and pain.
The patient scores each question on a scale from 0 (no pain or difficulty) to 10 (worst pain imaginable or so difficult it requires help), that best describes their foot over the past week.
Higher scores indicates worse pain. Both total and subcategory scores are calculated.
Time Frame
after wearing each insole for a week (at least 6 hours per day)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged between 20 and 65 years old
Appearance of decreased medial arch
Foot posture index score between 6 to 12
Exclusion Criteria:
History of injuries of the lower extremity within the past 6 months
Experience of use of orthopedic insole within the past 6 months
Acute disorders in the lower extremities and spine
History of surgery on the lower extremities and lumbar spine within the past 6 months
Facility Information:
Facility Name
Physical therapy center, national Taiwan university hosipital
City
Taipei
Country
Taiwan
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The Effect of Customized Insoles on Biomechanics and Pain in Patients With Functional Flatfoot
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