Closed-loop Medtronic 780G System in Youth With Type 1 Diabetes
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Medtronic 780G® hybrid closed loop.
- Who it may be relevant to
- Registry conditions: Type 1 Diabetes, Child, Only. Basic parameters: 1 year — 21 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Israel
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Title: Closed-loop Medtronic 780G System in Youth With Type 1 Diabetes: AWeSoMe Study Group Prospective Trial
Overview
The goal of this observational study is to describe data on Israeli children and youth using the 780G system including data regarding glycemic control parameters, various questionnaires, sleep data, bioimpedance measures, and dietary parameters. The main questions it aims to answer are: • whether the 780G system will improve glycemic control • whether the psychosocial aspects will improve. Participants will be followed once connected to 780G, at baseline, one, three, six months, 1 year, and two years after the connection.
Detailed description
Patients and Methods:
The study population will include individuals with type 1 diabetes ages 7-18 years who are managed by the pediatric diabetes teams from the AWeSoMe Study Group (five pediatric diabetes multidisciplinary clinics in Israel; Dana-Dwek Children's Hospital, Edmond and Lily Safra Children's Hospital, Maccabi National Juvenile Diabetes Center, Shamir Medical Center and Wolfson Medical Center) and who chose to purchase 780G out-of-pocket as part of their diabetes care, or are eligible according to the updated Israeli basket to receive it. The decision to use 780G will be made prior to and independent of their entrance to the study, and will be based on preferences of the patients and their parents.
Study design:
A prospective multi-center study (AWeSoMe Study Group) of type 1 diabetes patients using the closed-loop Medtronic 780G system as compared to their previous treatment regimen.
Data will be collected at 6 timepoints: baseline (at initiation of 780G system), after 1 month, three months and 6 months, 1 year, and 2 years of the closed-loop Medtronic 780G system usage.
Data collection:
All the data collected are available for healthcare providers (doctors, nurses and dieticians) as part of the routine diabetes clinic visit. The information retrieved from the medical files will include sociodemographic characteristics (current age, sex, socioeconomic position by home address, parent's education level, marital status of parents), anthropometric parameters (height, weight and body mass index), pubertal status, physical activity levels and diabetes-related characteristics. Diabetes-related characteristics: age at diagnosis, autoimmune co-morbidities (thyroid disease and Celiac), glycated hemoglobin (HbA1c) and acute complications (severe hypoglycemic episodes and DKA). Insulin pump and CGM downloaded data retrieved during the 2 weeks prior to the clinic visit: mode of insulin therapy (previous and current), total daily insulin dose (Units/kg/day), total daily carbohydrates (grams/day) and CGM metrics. CGM metrics will include: percent time CGM active, mean glucose level, standard deviation (SD), coefficient of variability (CV), time in range (TIR), time above range (TAR), time below range (TBR) and glucose management indicator (GMI). Closed-loop Medtronic 780G system user evaluation: reason for switching from conventional treatment to closed-loop, automode system exits and patient's/parent's perception of closed-loop system.
In addition to the data mentioned above the following data will be collected:
1. Questionnaires for the:
1. Patients - the quality of life, anxiety, fear of hypoglycemia - child, diabetes management, and nutrition knowledge in diabetes. All of the questionnaires are validated and were translated into Hebrew using the globally-accepted linguistic validation procedure. 2. Parents - the quality of life, fear of hypoglycemia - parent, diabetes management, sleep quality, and nutrition knowledge in diabetes. All of the questionnaires are validated and were translated into Hebrew using the globally-accepted linguistic validation procedure. 2. Bioimpedance parameters 3. Diet - nutrition evaluation through 3-daily diet notes 4. Sleep - sleep evaluation through parents' 3-daily sleep diaries
Interventions
- Device Medtronic 780G® hybrid closed loop
Medtronic 780G® hybrid closed loop system uses the commercial "auto-mode" with an insulin pump and continuous glucose monitoring.
Primary outcome measures
- Time spent in range (70-180 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0,3 months]
- Time spent in range (70-180 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0,6 months]
- Time spent in range (70-180 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0,12 months]
- Time spent in range (70-180 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0,24 months]
Secondary outcome measures (12)
- HbA1c as assessed from point-of-care clinic visit [Time frame: 0, 3 months]
- HbA1c as assessed from point-of-care clinic visit [Time frame: 0, 6 months]
- Time spent below range (≤ 70 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 3 months]
- Time spent below range (≤ 70 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 6 months]
- Time spent below range (≤ 54 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 3 months]
- Time spent below range (≤ 54 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 6 months]
- Time spent above range (> 180 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 3 months]
- Time spent above range (> 180 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 6 months]
- Time spent above range (> 250 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 3 months]
- Time spent above range (> 250 mg/dL) as assessed from closed-loop Medtronic 780G system [Time frame: 0, 6 months]
- Quality of life - child as assessed by a questionnaire [Time frame: 0, 6 months]
- Quality of life - parent as assessed by a questionnaire [Time frame: 0, 6 months]
Eligibility criteria
Inclusion criteria
Diagnosis of type 1 diabetes Diabetes duration ≥ 6 months Routine attendance at clinic visits Initiation of 780G system usage
Exclusion criteria
Children under the age of 1 year Children without 780G system
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
Israel · 1 center
- Sheba Medical Center — Ramat Gan
Publications
- Mehta SN, Nansel TR, Volkening LK, Butler DA, Haynie DL, Laffel LM. Validation of a contemporary adherence measure for children with Type 1 diabetes: the Diabetes Management Questionnaire. Diabet Med. 2015 Sep;32(9):1232-8. doi: 10.1111/dme.12682. Epub 2015 Jan 30. PMID 26280463
- Skinner TC, Hoey H, McGee HM, Skovlund SE; Hvidore Study Group on Childhood Diabetes. A short form of the Diabetes Quality of Life for Youth questionnaire: exploratory and confirmatory analysis in a sample of 2,077 young people with type 1 diabetes mellitus. Diabetologia. 2006 Apr;49(4):621-8. doi: 10.1007/s00125-005-0124-0. Epub 2006 Jan 26. PMID 16525844
- Gaudry E, Vagg P, Spielberger CD. Validation of the State-Trait Distinction in Anxiety Research. Multivariate Behav Res. 1975 Jul 1;10(3):331-41. doi: 10.1207/s15327906mbr1003_6. PMID 26829634
- Gonder-Frederick L, Nyer M, Shepard JA, Vajda K, Clarke W. Assessing fear of hypoglycemia in children with Type 1 diabetes and their parents. Diabetes Manag (Lond). 2011;1(6):627-639. doi: 10.2217/DMT.11.60. PMID 22180760
- Rovner AJ, Nansel TR, Mehta SN, Higgins LA, Haynie DL, Laffel LM. Development and validation of the type 1 diabetes nutrition knowledge survey. Diabetes Care. 2012 Aug;35(8):1643-7. doi: 10.2337/dc11-2371. Epub 2012 Jun 4. PMID 22665217
- Buysse DJ, Reynolds CF 3rd, Monk TH, Berman SR, Kupfer DJ. The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research. Psychiatry Res. 1989 May;28(2):193-213. doi: 10.1016/0165-1781(89)90047-4. PMID 2748771
- Gruber N, Wittenberg A, Brener A, Abiri S, Mazor-Aronovitch K, Yackobovitch-Gavan M, Averbuch S, Ben Ari T, Levek N, Levran N, Landau Z, Rachmiel M, Pinhas-Hamiel O, Lebenthal Y. Real-Life Achievements of MiniMed 780G Advanced Closed-Loop System in Youth with Type 1 Diabetes: AWeSoMe Study Group Multicenter Prospective Trial. Diabetes Technol Ther. 2024 Nov;26(11):869-880. doi: 10.1089/dia.2024.01 PMID 38758194
Identifiers
NCT: NCT05908708 · SHEBA-22-9609-NG-CTIL