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Path Active Multicentre Randomised Controlled Trial (Previous Pilot: Path Active; Safety and Tolerability Study)

Sponsor: Royal Free Hospital NHS Foundation Trust

NCT ID: NCT06084052

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Path Active (device), Control Group (other)
How long the study runs
Study runs about 23 months (dates as stated)
About the drug or intervention
Path Active — device: Participant use of Path Active insoles, mobile phone app and clinician's dashboard (where pressure and temperature changes can be reviewed by a clinician). · Control Group — other: Control Group will receive care as usual.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years to 100 Years
Who
All
Number of participants
120
Started
2024-04-02
Last checked
2025-04

Plain English Summary

What is this study?

  • • Testing a new treatment for diabetic foot
  • • NA - 120 participants
  • • Path Active™ comprises a pair of monitoring insoles which measure parameters associated with foot ulceration in diabetes: temperature and pressure

Who can take part?

  • • Ages 18 Years to 100 Years
  • • Diagnosed with diabetic foot

Where?

  • • London - Royal Free Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Path Active™ comprises a pair of monitoring insoles which measure parameters associated with foot ulceration in diabetes: temperature and pressure. The insoles are linked via an app to the wearer's mobile phone and also to a clinical dashboard so that both wearer and clinician are alerted to early signs of skin damage on the foot so that immediate preventive action can be taken. The study is a multisite randomised controlled trial which will evaluate the effectiveness of Path Active™ in 60 people with diabetes who are at 'high risk' of foot ulceration, compared with 60 people who receive their usual podiatry foot checks over a period of 12 weeks.

More detail

Foot complications in people with diabetes are the most common cause of non-traumatic leg amputation in the UK with over 176 leg, toe or foot amputations every week in England. One in seven people with diabetes will develop a foot ulcer at some stage in their lives. Not only does this impair their daily activities and reduce their quality of life, it also increases their risk of amputation by up to 24-fold. Five year mortality for minor and major amputations in diabetes have been reported as 46.2% and 56.6%, respectively. Circulatory problems, nerve impairment and infection contribute to foot complications in diabetes. Prior to a foot ulceration, changes in temperature and/or pressure occur. These early warning signs can be measured by Path Active™ and alert the wearer via a mobile phone app and the clinician via a clinical dashboard so that preventive action can be taken. Currently people with diabetes who have been assessed as 'high risk' for foot ulceration are allocated appointments with podiatrists in 'foot protection teams' who review on a weekly to monthly basis. Path Active™ has the potential to reduce appointments by alerting podiatry teams to potential problems as they occur rather than regular routine reviews. Path Active™ may be able to reduce hospital and clinic visits and thereby reduce healthcare carbon footprint. The primary objective of this clinical investigation is to evaluate the effectiveness of Path Active™ in people with diabetes who are at 'high risk' of foot ulceration. The study is a multisite randomised controlled trial which will evaluate the effectiveness of Path Active™ in 60 people with diabetes who are at 'high risk' of foot ulceration, compared with 60 people who receive their usual podiatry foot checks over a period of 12 weeks. Recruitment to the study will be in 4 clinical sites across England and Scotland. The protocol for this study was amended from the pilot study and accepted as a 'major amendment' by the regional Ethics Committee of Essex. Therefore the IRAS number (Unique Protocol ID: 326601) has remained the same.

Diabetic Foot

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years - 100 Years
  • Who can join: All genders

What the study is looking for

  • ✓• Participant able to give agreement to take part.
  • ✓Age \>18 at the time of consent.
  • ✓Diagnosis of Type 1 or Type 2 Diabetes.
  • ✓Both Feet Intact (no ulceration).
  • ✓Participant understands and is willing to participate and can comply with the follow-up regime.

Who cannot take part

  • ✗Either foot has less than 2 arterial vessel run-off on Doppler.
  • ✗Poor visual acuity ie registered blind, unless supported by carer.
  • ✗Current participation in another clinical investigation of a medical device or a drug; or participation in such a...
  • ✗Body Mass Index (BMI) \>40.
  • ✗Participant has bespoke contact insoles and footwear.
See the full criteria
Inclusion Criteria: * • Participant able to give informed consent. * Age \>18 at the time of consent. * Diagnosis of Type 1 or Type 2 Diabetes. * Both Feet Intact (no ulceration). * Participant understands and is willing to participate and can comply with the follow-up regime. * Participant diabetes foot Risk Stratification as 'High Risk' as in Frame (2021) Scotland/England https://www.diabetesframe.org/ * Ability to walk independently for \> 100 metres i.e without use of wheelchair, walking stick or personal assistance. * Participant able and willing to wear suitable footwear. * Must own a mobile phone and be willing to upload WWP app. Exclusion Criteria: * Either foot has less than 2 arterial vessel run-off on Doppler. * Poor visual acuity ie registered blind, unless supported by carer. * Current participation in another clinical investigation of a medical device or a drug; or participation in such a study within 30 days prior to study enrolment. * Body Mass Index (BMI) \>40. * Participant has bespoke contact insoles and footwear. * Participant is unable to use 'medium' or 'large' insoles due to foot size eg. small or extra large feet. * Participant has a pacemaker. * Participant is pregnant.

Where Is This Study? (1 UK site)

Royal Free Hospital

London NW3 2QE, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Richard Leigh, BSc

Sponsor contact

CONTACT

+44208302749 richardleigh1@nhs.net

Lise Pape, MSc

Sponsor contact

CONTACT

lise@walkwithpath.com
Data sourced from ClinicalTrials.gov · Last verified: 2025-04