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Shear and Pressure Reducing Insoles for the Diabetic Foot (GlideSoft)

Primary Purpose

Diabetes, Ulceration, Amputation

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
pressure reducing insole
GlideSoft®
Sponsored by
Diabetica Solutions Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetes focused on measuring friction, pressure, insole, ulcer, prevention

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of diabetes by WHO criteria
  • Ability to provide informed consent
  • 18-80 years of age

Exclusion Criteria:

  • Patients with open ulcers or open amputation sites
  • Active Charcot arthropathy
  • Severe peripheral vascular disease
  • Active foot infection
  • Dementia
  • Impaired cognitive function
  • History of drug or alcohol abuse within one year of the study
  • Other conditions based on the PI's clinical judgment

Sites / Locations

  • Kevin R. Higgins, DPM

Outcomes

Primary Outcome Measures

Incident foot ulcers

Secondary Outcome Measures

Full Information

First Posted
July 10, 2007
Last Updated
July 10, 2007
Sponsor
Diabetica Solutions Inc.
Collaborators
National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00499356
Brief Title
Shear and Pressure Reducing Insoles for the Diabetic Foot
Acronym
GlideSoft
Official Title
Shear and Pressure Reducing Insoles for the Diabetic Foot
Study Type
Interventional

2. Study Status

Record Verification Date
July 2007
Overall Recruitment Status
Completed
Study Start Date
May 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Diabetica Solutions Inc.
Collaborators
National Institutes of Health (NIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
We evaluated the feasibility of the GlideSoft™ novel insole to reduce pressure and shear forces on the foot. No commercially available insoles are designed to reduce shear. Although insurance providers spend millions on diabetics' therapeutic insoles, there is no scientific data about shear or pressure reduction. We will evaluate the optimal bonded materials from Phase I compared to the Glidesoft™ design using the same combination of viscoelastic materials. We evaluate 2 patient groups of 150 patients per arm (300 total) in an 18 month trial. The control group patient arm wore a traditional bonded insole whereas another the second arm receive the GlideSoft™. At baseline, and at the end of the 18 month trial, in-shoe gait lab and in vitro biomechanical parameters measured pressure, shear, and material properties as these changed with wear. This Phase II eighteen (18) month clinical trial evaluated the effectiveness of ShearSole™ reducing the incidence of diabetic ulcers. The overall study hypothesis was that GlideSoft™ provides significant shear reduction as compared to traditional insoles without sacrificing pressure reduction characteristics or durability.
Detailed Description
To evaluate the efficacy of a shear reducing shoe insole (GlideSoft) in reducing the incidence of diabetic foot pathology among high-risk patients. We studied the effectiveness of a shear reducing shoe insole to prevent foot ulcers in high-risk diabetics with sensory neuropathy, a history of a foot ulcer or a history of a partial foot amputation. The study comprised two treatment arms. The first group received standard therapy involving standard therapeutic shoes and insoles, patient education and regular foot evaluations by a physician. The second group received the same standard therapy, but instead of the standard insoles patients used the GlideSoft - a novel shear reducing insole. As determined in the Phase I study, the GlideSoft dramatically reduced shear forces compared to standard insoles, while performing equally well in reducing compressive forces. Patients were followed for 18 months. The primary study outcome was for incident foot ulcers. Our hypothesis was that patients who use the GlideSoft will have fewer ulcers and that these ulcers will be less severe compared to patients evaluated in the Standard Insole Group. To evaluate changes in pressure and shear reducing capabilities of the two. To evaluate changes in pressure and shear reducing capabilities of the GlideSoft and standard insoles over the duration of use. We measured in-shoe pressures and in-vitro shear forces at the foot-insole interface at the beginning of the study and after patients wore the insole for four months or one "standard cycle of wear". We used the Novel Electronics, Inc. Pedar in-shoe pressure system to measure the interface between the foot and insole and the Shear Force Tester (see Phase I report) to evaluate shear forces. We expected that the GlideSoft would significantly reduce shear forces and provide equivalent reduction in vertical forces at both the day 0 evaluation and day 120 evaluations. To evaluate patient perceived benefits, satisfaction, and compliance with the 2. To evaluate changes in pressure and shear reducing capabilities of the GlideSoft and standard insoles over the duration of use. We measured in-shoe pressures and in-vitro shear forces at the foot-insole interface at the beginning of the study and after patients wore the insole for four months or one "standard cycle of wear". We used the Novel Electronics, Inc. Pedar in-shoe pressure system to measure the interface between the foot and insole and the Shear Force Tester (see Phase I report) to evaluate shear forces. We expected that the GlideSoft would significantly reduce shear forces and provide equivalent reduction in vertical forces at both the day 0 evaluation and day 120 evaluations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Ulceration, Amputation, Foot Deformity, Neuropathy
Keywords
friction, pressure, insole, ulcer, prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
299 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
pressure reducing insole
Intervention Type
Device
Intervention Name(s)
GlideSoft®
Primary Outcome Measure Information:
Title
Incident foot ulcers
Time Frame
15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of diabetes by WHO criteria Ability to provide informed consent 18-80 years of age Exclusion Criteria: Patients with open ulcers or open amputation sites Active Charcot arthropathy Severe peripheral vascular disease Active foot infection Dementia Impaired cognitive function History of drug or alcohol abuse within one year of the study Other conditions based on the PI's clinical judgment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kevin R Higgins, DPM
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kevin R. Higgins, DPM
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78217
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17192326
Citation
Lavery LA, Higgins KR, Lanctot DR, Constantinides GP, Zamorano RG, Athanasiou KA, Armstrong DG, Agrawal CM. Preventing diabetic foot ulcer recurrence in high-risk patients: use of temperature monitoring as a self-assessment tool. Diabetes Care. 2007 Jan;30(1):14-20. doi: 10.2337/dc06-1600.
Results Reference
result
PubMed Identifier
23080240
Citation
Lavery LA, LaFontaine J, Higgins KR, Lanctot DR, Constantinides G. Shear-reducing insoles to prevent foot ulceration in high-risk diabetic patients. Adv Skin Wound Care. 2012 Nov;25(11):519-24; quiz 525-6. doi: 10.1097/01.ASW.0000422625.17407.93.
Results Reference
derived

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Shear and Pressure Reducing Insoles for the Diabetic Foot

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