A Comparison of Insoles Used to Prevent Neuropathic Diabetic Foot Ulceration
Primary Purpose
Diabetes, Neuropathic Foot
Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Insole
Sponsored by
About this trial
This is an interventional prevention trial for Diabetes focused on measuring Insoles, Prevention of Ulceration, Diabetic Foot, Neuropathic
Eligibility Criteria
Inclusion Criteria:
- diagnosed as having Type 1 or 2 diabetes mellitus, (recorded within the case notes and confirmed by participant),
- diagnosed with diabetic peripheral neuropathy
- palpable or biphasic pulses
- intact from lower limb vascular or neuropathic ulceration, scoring Grade 0 on the Wagner classification for foot ulcer
- able to walk a minimum of 10 metres unaided
- willing to comply with the requirements of the study.
Exclusion Criteria:
- presented with current or recently healed ulceration less than 6 months prior to study enrolment,
- severe fixed mid-foot or rearfoot deformity e.g. charcot joint, unsuitable for prefabricated insoles and non- bespoke footwear,
- history of major bone or joint surgery of the lower limb including major amputation
- unable to comprehend simple instructions and comply with the study protocols and procedures.
Sites / Locations
- Liskeard Community Hospital
- Local Care Center Mount Gould
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Custom made insole
Prefabricated Insole
Arm Description
Custom made functional moulded insole
Prefabricated accommodative moulded insole
Outcomes
Primary Outcome Measures
Reduction in peak pressure
Secondary Outcome Measures
Comparison of cost
Full Information
NCT ID
NCT00999635
First Posted
October 21, 2009
Last Updated
October 23, 2009
Sponsor
University of Plymouth
Collaborators
Cornwall and Illes of Scilly Primary Care Trust, Plymouth Teaching Primary Care Trust, Diabetes UK
1. Study Identification
Unique Protocol Identification Number
NCT00999635
Brief Title
A Comparison of Insoles Used to Prevent Neuropathic Diabetic Foot Ulceration
Official Title
A Comparison of Functional and Prefabricated Insoles Used for the Preventative Management of Neuropathic Diabetic Foot Ulceration: a Single Blind Randomised Control Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2009
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
September 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University of Plymouth
Collaborators
Cornwall and Illes of Scilly Primary Care Trust, Plymouth Teaching Primary Care Trust, Diabetes UK
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Importance of the topic:
Lower extremity amputation is a costly complication of diabetes for both the NHS and the patient. Amputation may be avoided if the preceding foot ulceration can be prevented. One method of reducing the risk of ulceration in the neuropathic foot is through the provision of therapeutic insoles. The type of insole prescribed (prefabricated verses custom made) is currently based on anecdotal evidence. The idea held by many practitioners that the custom made insole is superior in its effect remains speculation, unsupported by the evidence. In the absence of economic analysis, the available data suggests that the custom insole is substantially more expensive to the NHS. This study, to determine which of two types of insole used in therapeutic shoes reduces peak pressure more in the at-risk diabetic foot, is therefore a very important topic and will provide both useful evidence for the NHS podiatry services. It is of course also very important for patients with diabetes as the personal suffering of those undergoing amputation is immense.
The study is a single blind randomised controlled trial comparing custom made with 'off the shelf' insoles.
Detailed Description
Aim The study compared custom-made functional insoles with prefabricated insoles for the preventative management of neuropathic diabetic feet, assessing effects on peak pressure, forefoot pressure time integral, total contact area, forefoot rate of loading, duration of load as a percentage of stance, quality of life, perceived foot health and cost.
Method Pilot work investigating the physical properties of materials used to fabricate insoles informed material selection. A single-blind randomised control trial recruited 119 neuropathic participants with diabetes from two Primary Care Trusts and randomly allocated them to either custom-made functional insoles or prefabricated insoles. Data was collected at issue and 6-month follow-up, using the F-scan in-shoe pressure measurement system. Patient perceptions were assessed with the Bristol Foot Score and Audit of Diabetes Dependant Quality of Life. Further analyses were carried out on two subgroups; 1) insole effect on peak pressure in 44 participants with pronated feet, over a 6-month follow-up period; 2) insole durability, investigated in a second subgroup of 60 participants for 12-months. Durability was evaluated in terms of change in insole thickness and reduction in peak pressure.
To increase the robustness of results, data analysis was calculated using three strategies; 1) pure intention-to-treat analysis, including all 119 participants randomised to an intervention; 2) intention-to-treat analysis, using all available data; 3) as-treated analysis, including those participants self-reporting full insole compliance, defined as 60% or more daytime wear.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Neuropathic Foot
Keywords
Insoles, Prevention of Ulceration, Diabetic Foot, Neuropathic
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
119 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Custom made insole
Arm Type
Experimental
Arm Description
Custom made functional moulded insole
Arm Title
Prefabricated Insole
Arm Type
Active Comparator
Arm Description
Prefabricated accommodative moulded insole
Intervention Type
Device
Intervention Name(s)
Insole
Intervention Description
Comparison of custom made and prefabricated insoles designed for the neuropathic diabetic foot, issued for day time wear and followed for a 6 month period
Primary Outcome Measure Information:
Title
Reduction in peak pressure
Time Frame
6-months
Secondary Outcome Measure Information:
Title
Comparison of cost
Time Frame
6-months
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diagnosed as having Type 1 or 2 diabetes mellitus, (recorded within the case notes and confirmed by participant),
diagnosed with diabetic peripheral neuropathy
palpable or biphasic pulses
intact from lower limb vascular or neuropathic ulceration, scoring Grade 0 on the Wagner classification for foot ulcer
able to walk a minimum of 10 metres unaided
willing to comply with the requirements of the study.
Exclusion Criteria:
presented with current or recently healed ulceration less than 6 months prior to study enrolment,
severe fixed mid-foot or rearfoot deformity e.g. charcot joint, unsuitable for prefabricated insoles and non- bespoke footwear,
history of major bone or joint surgery of the lower limb including major amputation
unable to comprehend simple instructions and comply with the study protocols and procedures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ray Jones, Professor
Organizational Affiliation
University of Plymouth
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Joanne Paton, PhD
Organizational Affiliation
University of Plymouth
Official's Role
Principal Investigator
Facility Information:
Facility Name
Liskeard Community Hospital
City
Liskeard
State/Province
Cornwall
Country
United Kingdom
Facility Name
Local Care Center Mount Gould
City
Plymouth
State/Province
Devon
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
23216959
Citation
Paton JS, Stenhouse EA, Bruce G, Zahra D, Jones RB. A comparison of customised and prefabricated insoles to reduce risk factors for neuropathic diabetic foot ulceration: a participant-blinded randomised controlled trial. J Foot Ankle Res. 2012 Dec 5;5(1):31. doi: 10.1186/1757-1146-5-31.
Results Reference
derived
Learn more about this trial
A Comparison of Insoles Used to Prevent Neuropathic Diabetic Foot Ulceration
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