Insole Optimisation for Ulcer Prevention: a Feasibility Trial

NCT01948479 | Unknown

• 1 other identifier: PatonRCT02
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

Insoles are designed to reduce increased loads and re-ulceration risk in patients with diabetes. The investigators previous research findings suggest that an instant insole solution may benefit some, but effectiveness is difficult to predict. The investigators propose a feasibility study using in-shoe pressure analysis to optimise the protective effect of insoles and footwear with the aim of reducing re-ulceration rates. Early indications from exploratory case studies within the real world clinical setting suggest that by implementing the investigators previous published research findings the investigators can optimise effectiveness and reduce outcome variability of protective footwear and insoles provided to patients at risk of re-ulceration. However a further randomised control trial is necessary to evaluate the effectiveness of in-shoe pressure analysis in reducing re-ulceration rates within the NHS setting. The proposed feasibility study will recruit 20 participants from the multidisaplinary diabetic foot clinic Derriford Hospital and allocate them to either 1) Routine insoles and footwear provision or 2) Routine insole and footwear provision, and temporary insole provision with optimisation. The findings from the feasibility study will inform protocol development for a larger clinical trial. The results of the feasibility study will be used to strengthen a protocol for a grant application to conduct the main RCT. A secondary output from the pilot study will be the dissemination of findings in a peer reviewed journal and at conference.

Conditions

Diabetic; Neuropathic; Past Ulceration

Outcome Measures

Primary Outcomes (1)

• ulcer recurrence rates

  6 months

Secondary Outcomes (1)

• peak pressure reduction with the addition of the intervention

  Issue and 6 months

Study Arms (2)

Insole optimised with inshoe analysis

EXPERIMENTAL

Device: Optimised instant offloading insole

Routine insole provision

ACTIVE COMPARATOR

Device: Optimised instant offloading insole

Interventions

Optimised instant offloading insole DEVICE

Insole optimised with inshoe analysis; Routine insole provision

Eligibility Criteria

• Age: 30 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Participant is willing and able to give informed consent for participation in the study.
• Male or Female, aged 30 years or above
• Diagnosed with Diabetes Mellitus
• Recently healed/healing target ulcer on the weight-bearing surface of the foot
• Neuropathic (Mild to moderate DPN defined as insensitivity of a 10 g monofilament at 1-3 sites in the following locations: hallux, 1st, 3rd, and 5th metatarsal heads (Boulton AJ, Armstrong DG, Albert SF, Frykberg RG, Hellman R, Kirkman MS, Lavery LA, Lemaster JW, Mills JL Sr, Mueller MJ, Sheehan P, Wukich DK: Comprehensive foot examination and risk assessment: a report of the task force of the foot care interest group of the American Diabetes Association, with endorsement by the American Association of Clinical Endocrinologists. Diabetes Care 2008;31:1679-1685)
• Able (in the Investigators opinion) and willing to comply with all study requirements

You may not qualify if:

• The participant may not enter the study if ANY of the following apply: Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.
• None healing foot ulcer at another site that requires targeted off-loading.
• Unable to walk 5 metres with/without walking aid
• Peripheral vascular disease (non-re-constructible vascular disease as determined by arterial duplex and clinically assessed by a vascular consultant)
• Unwilling to wear therapeutic footwear
• Where amputation has been part of the current episode of care and includes ulceration site.

Sponsors & Collaborators

• University of Plymouth: lead
• University Hospital Plymouth NHS Trust: collaborator

Study Sites (1)

Derriford Hospital

Plymouth, Devon, PL6 8BH, United Kingdom

Location

Central Study Contacts

Joanne Paton, PhD

CONTACT

01752 588845; joanne.paton@plymouth.ac.uk

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: NIHR Clinical Research Fellow

Study Record Dates

• First Submitted: September 18, 2013
• First Posted: September 23, 2013
• Study Start: January 1, 2014
• Primary Completion: January 1, 2015
• Study Completion: January 1, 2015
• Last Updated: September 26, 2013

Record last verified: 2013-09

Locations

GB (1)