The classic website will no longer be available as of June 25, 2024. Please use the modernized ClinicalTrials.gov.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

In-shoe Pressures Associated With Footwear Fit Guidelines

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT06025422
Recruitment Status : Recruiting
First Posted : September 6, 2023
Last Update Posted : May 1, 2024
Sponsor:
Collaborator:
University of Salford
Information provided by (Responsible Party):
University Hospitals, Leicester

Brief Summary:

One in five foot ulcers are caused by the footwear worn by people with diabetes, yet there is a lack of consensus around footwear fit. Recommended toe gaps (the gap between the longest toe and the inside of the shoe) vary depending on the footwear guidance referred to but no research to date has assessed the recommendations' effectiveness in minimising in-shoe pressures.

The investigators will carry out a pilot study in 60 people with diabetes and loss of foot sensation (neuropathy). In this study, the investigators will measure in-shoe pressures whilst participants walk at the same pace to the beat of a metronome. An insole placed inside participants' shoes will measure in-shoe pressures. Participants will wear the same (standardised) type of footwear. The study is designed to detect a difference in pressure within this made-to-measure footwear whose fit conforms to Standard 1 guidance compared with footwear whose fit conforms to Standard 2 guidance. Differences between Standards 1 and 2 with Standard 3 will be considered secondary analyses. Standards are simplified to three non-overlapping recommended toe gap ranges of 0.5-1.0cm; 1.5-2.0cm and 1.0-1.5cm.

The investigators will also analyse the heat images taken with a thermographic camera before and after walking in standardised footwear whose fit confirms to these standards (this is known as the plantar thermal stress response to walking). Footwear fit will be determined by measuring the dimensions of participants' feet and that of participants' footwear and comparing the two.

The investigators will also measure footwear fit and associated in-shoe pressure/plantar thermal stress response in participants' habitual footwear during walking at paced and self-selected speeds.


Condition or disease
Diabetic Foot Ulcer Diabetic Neuropathies

Show Show detailed description

Layout table for study information
Study Type : Observational
Estimated Enrollment : 60 participants
Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Evaluation of Footwear Fit Guidelines Under Pressure in At-Risk Feet
Actual Study Start Date : March 13, 2023
Estimated Primary Completion Date : November 29, 2024
Estimated Study Completion Date : November 29, 2024

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Foot Health




Primary Outcome Measures :
  1. During the procedure difference in mean in-shoe PPP associated with each toe gap standard within standardised footwear @ regulated pace [ Time Frame: During the procedure, peak plantar pressure in kilopascals (kPa) is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure Difference in the mean average in-shoe peak plantar pressure (PPP) associated with each toe gap standard (measured by Pedar-X pressure monitoring insoles) during walking within standardised footwear at a regulated pace

  2. During the procedure difference in the mean in-shoe PPP by ROI associated with each toe gap standard [ Time Frame: During the procedure, peak plantar pressure in kilopascals (kPa) is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure Mean in-shoe peak plantar pressure (PPP) for each region of interest (ROI) (comprising 10 regions: hallux, toes 2/3, toes 4/5, metatarsal 1, metatarsal 2/3, metatarsal 4/5, medial midfoot, lateral midfoot, medial heel, lateral heel) associated with each toe gap standard during walking within standardised footwear at a regulated pace


Secondary Outcome Measures :
  1. During the procedure Exploratory secondary analysis of toe gap Standard 3 in relation to toe gap Standards 1 and 2 [ Time Frame: During the procedure, peak plantar pressure in kilopascals (kPa) is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure Differences in mean average in-shoe peak plantar pressure associated with toe gap Standards 1 and 2 with Standard 3 will be considered secondary analyses.

  2. During the procedure Pressure time integral & contact area associated with toe gap standards in standardised footwear [ Time Frame: During the procedure, peak plantar pressure in kilopascals (kPa) is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure Pressure time integral and contact area associated with each toe gap standard during walking within standardised footwear at a regulated pace

  3. During the procedure Proportion of participants with in-shoe PPP > 200 kilopascals in standardised footwear [ Time Frame: During the procedure, peak plantar pressure in kilopascals (kPa) is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure The proportion of participants where the mean in-shoe peak plantar pressure (PPP) at the forefoot, toes or metatarsal regions exceeds 200 kPa or for the plantar region as a whole during walking in standardised footwear at a regulated pace

  4. During the procedure PTSR associated with each toe gap standard in standardised footwear [ Time Frame: Thermal image taken with FLIR T540-EST thermal camera of plantar surface of feet at rest and after 200 steps within standardised footwear ]
    During the procedure Plantar thermal stress response (PTSR) is defined as changes in 95th percentile temperature values in Celsius when comparing thermal images of the plantar surface of the feet at rest prior to walking and a thermal image of the feet after walking for each region of interest (forefoot, midfoot, rearfoot) associated with each toe gap standard whist walking in standardised footwear at regulated pace

  5. During the procedure Mean in-shoe PPP within habitual footwear at a self-selected and regulated pace [ Time Frame: During the procedure, peak plantar pressure in kilopascals (kPa) is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure Mean in-shoe peak plantar pressure overall and for each region of interest (comprising 10 regions: hallux, toes 2/3, toes 4/5, metatarsal 1, metatarsal 2/3, metatarsal 4/5, medial midfoot, lateral midfoot, medial heel, lateral heel) associated with each toe gap standard during walking within habitual footwear at a self-selected and regulated pace

  6. During the procedure Proportion of participants with in-shoe PPP > 200 kilopascals in habitual footwear [ Time Frame: During the procedure, peak plantar pressure in kilopascals (kPa) is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure The proportion of participants where the mean in-shoe peak plantar pressure at the forefoot, toes or metatarsal regions exceeds 200 kPa or for the plantar region as a whole during walking in habitual footwear at a regulated and self-selected pace

  7. During the procedure Pressure time integral & contact area associated with toe gap standards in habitual footwear [ Time Frame: During the procedure, pressure time integral and contact area is measured with Novel Pedar pressure measuring insoles and software whilst completing 4 x 12 midgait steps at a speed of 2 miles per hour +/- 5% ]
    During the procedure Pressure time integral and contact area associated with each toe gap standard during walking within habitual footwear at a regulated pace

  8. During the procedure Percentage of participants with incorrectly fitted / correctly fitted habitual footwear [ Time Frame: At presentation on visit 2 ]
    During the procedure The percentage of participants with incorrectly fitted / correctly fitted habitual footwear as defined by each standard and the mean, minimum, maximum and standard deviation of toe gaps found within their habitual footwear

  9. During the procedure PTSR associated with habitual footwear [ Time Frame: Thermal image taken with FLIR T540-EST thermal camera of plantar surface of feet at rest and after 200 steps within habitual footwear ]
    During the procedure Plantar thermal stress response (PTSR) is defined as changes in 95th percentile temperature values in Celsius when comparing thermal images of the plantar surface of the feet at rest prior to walking and a thermal image of the feet after walking for each region of interest (forefoot, midfoot, rearfoot) associated with each toe gap standard whist walking in habitual footwear



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Sixty people with diabetes type 1 or 2 and neuropathy aged between 18 and 80
Criteria

Inclusion Criteria:

  • Men and women aged 18-80 years
  • Confirmed diagnosis of diabetes mellitus type 1 or type 2
  • Confirmed diagnosis of neuropathy;
  • Able to walk unaided for a minimum of 200 steps with capacity to attend the research site
  • PAR-Q physical activity questionnaire does not indicate any possible heart problems, dizziness or other issue indicating unsuitability for mild physical exercise involved in walking
  • Willingness and capacity to participate in the study and to sign the informed consent form

Exclusion Criteria:

  • Unconfirmed diabetes mellitus diagnosis
  • Inability to ambulate independently without walking aids
  • Presence of rheumatoid arthritis
  • Active ulcer (i.e. having an active ulcer at the time of recruitment)
  • Recently healed ulcer (an ulcer which has had less than six months to fully heal)
  • History of Charcot in foot/joints
  • Previous minor or major amputation
  • Neurological disorders other than diabetes-related neuropathy potentially affecting gait, balance or posture
  • Evidence of significant peripheral vascular disease e.g. (i) attendance at a specialist vascular clinic; (ii) documentation of occlusive arterial disease or intervention; (iii) at least one pulse should be palpable on the affected foot with exclusion where neither pulse is palpable
  • Blood pressure >180/100 or <90/50
  • Unable to understand written and verbal English
  • PAR-Q physical activity questionnaire indicates possible heart problems, dizziness or other issue indicating unsuitability for mild physical exercise involved in walking

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06025422


Contacts
Layout table for location contacts
Contact: Petra J Jones 0116 258 4974 pj100@leicester.ac.uk

Locations
Layout table for location information
United Kingdom
Leicester Diabetes Centre Recruiting
Leicester, Leicestershire, United Kingdom, LE5 4PW
Contact: Rachel Berrington    0116 258 4898    Rachel.berrington@uhl-tr.nhs.uk   
Sponsors and Collaborators
University Hospitals, Leicester
University of Salford
Investigators
Layout table for investigator information
Principal Investigator: Petra J Jones University Hospitals, Leicester
Layout table for additonal information
Responsible Party: University Hospitals, Leicester
ClinicalTrials.gov Identifier: NCT06025422    
Other Study ID Numbers: edge136945
20/0006190 ( Other Grant/Funding Number: Diabetes UK )
273255 ( Other Identifier: Health Research Authority (IRAS no.) )
First Posted: September 6, 2023    Key Record Dates
Last Update Posted: May 1, 2024
Last Verified: September 2023

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University Hospitals, Leicester:
in-shoe peak plantar pressure
plantar thermal stress response
diabetes footwear fit
toe gap
Additional relevant MeSH terms:
Layout table for MeSH terms
Diabetic Neuropathies
Diabetic Foot
Foot Ulcer
Diabetic Angiopathies
Vascular Diseases
Cardiovascular Diseases
Leg Ulcer
Skin Ulcer
Skin Diseases
Diabetes Complications
Diabetes Mellitus
Endocrine System Diseases
Foot Diseases
Peripheral Nervous System Diseases
Neuromuscular Diseases
Nervous System Diseases