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.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
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
Where Is This Study? (1 UK site)
Royal Free Hospital
London NW3 2QE, United Kingdom
How to Get in Touch
Richard Leigh, BSc
Sponsor contactCONTACT
Lise Pape, MSc
Sponsor contactCONTACT
