Tele-homecare Service for Diabetic Foot Patients (Risk 0, Risk 1 and Risk 2 Level): Testing and Validation of Dedicated APPs and Artificial Intelligence Solutions (MYFOOT-D)

April 13, 2023 updated by: Faculty Hospital AGEL Skalica

MY FOOT project aims at filling the gap in mobile applications by providing evidence to both involved stakeholders, that is the remote assistance from the hospital and the patient, who is directly involved in their own care strategy.

In particular, the application has to motivate patients and engage them in their self-care. Interaction with the mobile phone application is in the following terms:

APP elaborates data input from the patient in terms of own feeling of health status, symptoms revealed along the day, events eventually occurred, photos of the foot, including ulcer zoom (if any), APP reports back about increase / decrease in the Risk Level graph through time, maps the ulcer evolution or healing based on photos elaboration, using adequate graphs reporting time in the main axis, whilst reminds personal goals to enact care on a regular basis on the basis of the current conditions, eventually alerts the patient to contact clinicians for a visual inspection at a hospital.

Study Overview

Detailed Description

Without effective self-care, people with diabetic foot ulcers (DFUs) are at risk of prolonged healing times, hospitalization, amputation, and reduced quality of life. Despite these consequences, adherence to DFU self-care remains low.

As already pointed out in the preceding paragraphs, patient education in the prevention of diabetic foot ulcers found has been recognised as providing positive short-term effects on knowledge about care of the foot, delaying foot ulceration and amputation, especially in high-risk patients. New strategies are needed to engage people in the self-care of their DFUs.

Modern information technology may assist in attracting patients' interest if any direct benefit is promptly perceived by the patient who uses it . It is also of utmost importance that health professionals, especially those who work with diabetic patients on a daily basis, are aware of such practices and then be able to convince patients they merit the best care possible to avoid any further degradation of the pathology.

Mobile health apps hold great promise for people with diabetes, but few apps seek to engage people in their DFU self-care , , .

Schäfer et al. examined the risk factors of developing diabetic foot ulcers and amputation among patients with diabetes. They concluded that prediction and on-time treatment of diabetic foot ulcers (DFU) are of great importance for improving and maintaining patients' quality of life and avoiding the consequent socio-economic burden of amputation.

Machine learning is a part of the field of artificial intelligence, which can automatically learn models from data and better inform clinical decision-making. Xie et al. developed an accurate and explainable prediction model to estimate the risk of in-hospital amputation in 618 hospitalized patients with DFU. They concluded that machine learning model provided accurate estimates of the amputation rate in patients with DFU during hospitalisation. Besides, the model could inform individualised analyses of the patients' risk factors.

The severe complications associated with diabetes include diabetic ketoacidosis, nonketotic hypersmolar coma, cardiovascular disease, stroke, chronic renal failure, retinal damage and foot ulcers. There is a huge increase in the number of patients with diabetes globally and it is considered a major health problem worldwide. Early diagnosis of diabetes is helpful for treatment and reduces the chance of severe complications associated with it. Machine learning algorithms (such as ANN, SVM, Naive Bayes, PLS-DA and deep learning) and data mining techniques are used for detecting interesting patterns for diagnosing and treatment of disease. Current computational methods for diabetes diagnosis have some limitations and are not tested on different datasets or people from different countries which limits the practical use of prediction methods .

A system deploying artificial intelligence and machine learning, developed by a startup based in Vrnjacka banja (Serbia), can help predict the development of complications in the feet of diabetic patients.

MY FOOT project aims at filling the gap in mobile applications by providing evidence to both involved stakeholders, that is the remote assistance from the hospital and the patient, who is directly involved in their own care strategy.

In particular, the application has to motivate patients and engage them in their self-care. Interaction with the mobile phone application is in the following terms:

APP elaborates data input from the patient in terms of own feeling of health status, symptoms revealed along the day, events eventually occurred, photos of the foot, including ulcer zoom (if any), APP reports back about increase / decrease in the Risk Level graph through time, maps the ulcer evolution or healing based on photos elaboration, using adequate graphs reporting time in the main axis, whilst reminds personal goals to enact care on a regular basis on the basis of the current conditions, eventually alerts the patient to contact clinicians for a visual inspection at a hospital.

Study Type

Observational

Enrollment (Anticipated)

100

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Recruitment will be performed from the ranks of guests of the Special Hospital Merkur, who come to the program from all over the Republic of Serbia. That is why Merkur is in contact with colleagues from all health centers throughout Serbia, which have diabetes counseling centers.

From 5 to 8 patients with diabetes will be invited weekly to recruit the required number of participants in the pilot.

AGEL: Diabetic foot patients are distributed in different health centres of the Serbian cluster. Four diabetic outpatient units will refer patients by their responsible physicians according to inclusion and exclusion criteria. There are already more than 800 patients follow up in home environment.

Description

Inclusion Criteria:

  • The sample will include all the people accommodated in Special hospital Merkur, who sign the informed consent. Patients aged between 18 and 80 years. Patients diagnosed with Diabetes Mellitus (more than 5 years from diagnosis). Participant has adequate circulation to the affected extremity(ies), as demonstrated by at least ONE of the following within 60 days prior to enrolment/randomization: a) Dorsum transcutaneous oxygen test (TcPO2) of study leg(s) with results ≥40mmHg, OR, b) Ankle-Brachial Index (ABI) of study leg(s) with results of ≥ 0.7 and ≤ 1.3, OR; C) Toe-Brachial Index (TBI) of study extremity(ies) with results of ≥ 0.5.

Exclusion Criteria:

  • People who do not give their consent to participate in the study, who do not have a mobile phone, or live in an area not covered by a mobile signal and the Internet. Participant who is pregnant, breast feeding or planning to become pregnant. Participant having multiple foot ulcers, an amputation of the forefoot or an amputation at a more proximal location of the foot. Participant having a cancer disease or life expectancy less than six months as assessed by the investigator or undergoing cancer treatment; Participant having a severe foot infection; Active infection, undrained abscess, or critical colonization of the wound(s) with bacteria in the judgment of the investigator; Participant with Hgb A1c > 12 percent within 3 months prior to randomization; Participant with a known history of poor compliance with medical treatments.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Detection of vascular disorders
Time Frame: 12 months
The diabetes care is implemented by highly qualified health care professionals and continuously supervised by the leading experts from the university hospitals in Serbia. Moreover, the professors of endocrinology, neurology, vascular surgeon and diabetology from the medical universities of Belgrade and Kragujevac and AGEL supervise all those activities
12 months
Detection of neurological disorders
Time Frame: 12 months
The diabetes care is implemented by highly qualified health care professionals and continuously supervised by the leading experts from the university hospitals in Serbia. Moreover, the professors of endocrinology, neurology, vascular surgeon and diabetology from the medical universities of Belgrade and Kragujevac and AGEL supervise all those activities
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Analysing of potential risk factors contributed into Risk 0 and 1
Time Frame: 12 months
o fill the gap of mobile applications in providing evidence to both involved stakeholders, that is the remote assistance from the hospital and the patient, who is directly involved in own care strategy
12 months
Analysing of potential precipitating factors for DFU
Time Frame: 12 months
o fill the gap of mobile applications in providing evidence to both involved stakeholders, that is the remote assistance from the hospital and the patient, who is directly involved in own care strategy
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

September 1, 2023

Primary Completion (Anticipated)

September 1, 2025

Study Completion (Anticipated)

September 1, 2026

Study Registration Dates

First Submitted

April 13, 2023

First Submitted That Met QC Criteria

April 13, 2023

First Posted (Actual)

April 26, 2023

Study Record Updates

Last Update Posted (Actual)

April 26, 2023

Last Update Submitted That Met QC Criteria

April 13, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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