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

NHS Foundation Trust

Status: Enrolling

Conditions: Diabetic Foot

Treatments: Device: Path Active; Other: Control Group

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06084052

326601

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 120 estimated patients

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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120 participants in 2 patient groups

Path Active

Other group

Description:

Participants randomised to use the device

Treatment:

Device: Path Active

Control Group

Other group

Description:

Participants randomised to care as usual

Treatment:

Other: Control Group