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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01955031
Other study ID # 12 424 03
Secondary ID PREPS
Status Completed
Phase N/A
First received
Last updated
Start date November 2013
Est. completion date July 2019

Study information

Verified date August 2021
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Severity of diabetes is related to the development of disabling and costly complications (12.9 billion euros in 2007). The French High Health Authority recommends a therapeutic education on lifestyle and dietary rules in first-line treatment of Type 2 Diabetes Mellitus. Despite these recommendations, patients often have difficulties to implement dietary recommendations every day. The objective of EDUC@DOM is to help people with diabetes to improve lifestyle and equilibrium of glycaemia in order to avoid or delay chronic complications of diabetes. Our main goal is to assess effectiveness of our telemonitoring program in type 2 patients' care compared to a usual care of diabetes, on the glycaemia of the patients. It is expected that our program leads to a better monitoring of health status, a greater adherence to medical and non-medical prescriptions, an empowerment of the patient, and as a consequence, a more efficient health care consumption.


Recruitment information / eligibility

Status Completed
Enrollment 282
Est. completion date July 2019
Est. primary completion date May 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient with type 2 diabetes - Older than 18 years - With an insulin treatment or not - Having a glycemic impairment characterized by 6.5% <HbA1c =10 - Having an active internet connection at home. - Accepting the terms of training, loan and use of the device - Benefiting from social protection system - Having given his/her free and informed consent and signed the consent Exclusion Criteria: - Serious illness recently (<3 months) or decompensated may influence glycemic control of the patient permanently according to the judgment of the physician in charge of monitoring - Retinal state that does not allow optimization in equilibrium of glycaemia - Known severe renal impairment defined by creatinine clearance <30ml/min - Known hemoglobinopathy - Visual or intellectual resulting inability to use the remote monitoring tool according to the judgment of the physician in charge of monitoring - Inability to understand all or part of the software information according to the judgment of the physician in charge of monitoring - Subject to disabled - Person with severe behavioral disorders (anorexia, bulimia, ...) according to the judgment of the physician in charge of monitoring - Person who had, or in preparation for bariatric surgery (software nutrition education are not suitable for this type of care.) - Person with a medical device implanted electronic pacemakers and defibrillators with cardiac (possibility of interference with the impedance) - Another person involved in research including a period of ongoing exclusion to inclusion, - A person under legal protection - Subject living in institutions - Desire for pregnancy, pregnancy or breastfeeding

Study Design


Related Conditions & MeSH terms


Intervention

Other:
telemonitoring
A telemonitoring program with educational tools is given to people with type 2 diabetes at their home. It is composed of three softwares to improve eating habits available on touchpad, a self-monitoring blood glucose device, a balance to measure weight and fat mass, and a pedometer to evaluate physical activity. Data are securely sent and stored into a web service which delivers a synthesis to patients and health professionals.
Usual care
Patients are recruited during therapeutic educational sessions or appointments by general practitioners or diabetologists who take part into the Regional Health Network in Diabetes DIAMIP. If patients accept to participate to the study and sign up the protocol consent, they are given questionnaires about nutrition, physical activity and quality of life. A dietician analyses with each patient the results of a food inquiry. Patients are randomised into two groups: one arm is trained to the telemonitoring program before receiving it at home, and the other arm follows usual care. During 12 months, the telemonitoring group uses the device. The investigators (GP or diabetologists) can use the specific secured website to follow the measured parameters and to make appropriate decisions about health care of their patient. No consultation are scheduled in advance.

Locations

Country Name City State
France University Hospitals of Toulouse (Rangueil and Salies-Du-Salat) Toulouse Midi-Pyrénées

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

References & Publications (59)

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* Note: There are 59 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary To assess effectiveness of our telemonitoring program in Diabetes care, HbA1C assays will be compared between the two groups.The change of HbA1c between day 0, month 1,month 3, month 6, month 9 and month 12 HbA1c will be measured at Day 0, month 1, month 3, month 6, month 9 and month 12
Secondary Assessment efficacy of our program by the measure of HbA1C will At month 15, month 18, month 21 and month 24
Secondary Questionnaires will be given to patients to assess the improvement of nutritional knowledge At day 0 and month 24
Secondary Food inquiries will be given to patients to assess the improvement of eating habits At day 0 and month 24
Secondary Questionnaires will be given to patients to assess the physical activity practice At day 0 and month 24
Secondary Waist circumference will be measured to assess the body composition, BMI (Body Mass Index), At day 0 and month 24
Secondary The self-monitoring blood glucose books will be copied to assess mean of blood glycaemia At day 0, month 12 and month 24
Secondary A blood sample will be collected to assess lipid status At day 0 and month 24
Secondary Two questionnaires will be given to patients to assess quality of life of patients At day 0 and month 24
Secondary A cost-effectiveness ratio and a markov modelisation will be realized to assess the economic aspects At month 24
Secondary For the telemonitoring arm, assessment of food behavior through meals registered with the Nutri-Educ software Everytime patients use the software from Day 0 to month 24
Secondary For the telemonitoring arm, assessment of nutritional knowledge through rate of good choices playing games of Nutri-Kiosk software Everytime patients use the software from Day0 to month 24
Secondary For the telemonitoring arm, assessment of physical activity declared through Acti-Kiosk software and measures collected with the pedometer (number of steps, number of stairs climbed up) Every time patients use the software and the pedometer from day 0 to month 24
Secondary For the telemonitoring arm, measure of weight, fat rate and lean rate collected with the balance Everytime patients use the balance from day 0 to month 24
Secondary For the telemonitoring arm, means of glycaemia collected with the self-monitoring blood glucose device Everytime patients use the blood glucose device from day 0 to month 24
Secondary For the telemonitoring arm, acceptability and satisfaction of the telemonitoring system by the patients with the number and time of connections and a questionnaire At month 24
Secondary For the telemonitoring arm, acceptability and satisfaction of the telemonitoring system by the health professionals with the number and time of connections At month 24
Secondary For the telemonitoring arm, acceptability and satisfaction of the telemonitoring system by the health professionals with the number and time of connections leading to a medical decision (phone call or medical appointment) and a questionnaire At month 24
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