Closed-loop Medtronic 780G System in Youth With Type 1 Diabetes

Sponsor
Sheba Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT05908708
Collaborator
Tel-Aviv Sourasky Medical Center (Other), Assaf-Harofeh Medical Center (Other), Maccabi Healthcare Services, Israel (Other), Wolfson Medical Center (Other)
120
1
12
10

Study Details

Study Description

Brief Summary

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, and six months after the connection.

Condition or Disease Intervention/Treatment Phase
  • Device: Medtronic 780G® hybrid closed loop

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 4 timepoints: baseline (at initiation of 780G system), after 1 month, three months and 6 months 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:

  2. 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.

  3. 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.

  4. Bioimpedance parameters

  5. Diet - nutrition evaluation through 3-daily diet notes

  6. Sleep - sleep evaluation through parents' 3-daily sleep diaries

Study Design

Study Type:
Observational
Anticipated Enrollment :
120 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Title: Closed-loop Medtronic 780G System in Youth With Type 1 Diabetes: AWeSoMe Study Group Prospective Trial
Actual Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Outcome Measures

Primary Outcome Measures

  1. Time spent in range (70-180 mg/dL) as assessed from closed-loop Medtronic 780G system [0,3 months]

    Change in time spent in range (70-180 mg/dL) from baseline to three months of closed-loop Medtronic 780G system

  2. Time spent in range (70-180 mg/dL) as assessed from closed-loop Medtronic 780G system [0,6 months]

    Change in time spent in range (70-180 mg/dL) from baseline to six months of closed-loop Medtronic 780G system

Secondary Outcome Measures

  1. HbA1c as assessed from point-of-care clinic visit [0, 3 months]

    Change in HbA1c from baseline to three months of closed-loop Medtronic 780G system

  2. HbA1c as assessed from point-of-care clinic visit [0, 6 months]

    Change in HbA1c from baseline to six months of closed-loop Medtronic 780G system

  3. Time spent below range (≤ 70 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 3 months]

    Change in time spent below range (≤ 70 mg/dL) baseline to three months of closed-loop Medtronic 780G system

  4. Time spent below range (≤ 70 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 6 months]

    Change in time spent below range (≤ 70 mg/dL and ≤ 54 mg/dL) baseline to six months of closed-loop Medtronic 780G system

  5. Time spent below range (≤ 54 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 3 months]

    Change in time spent below range (≤ 54 mg/dL) baseline to three months of closed-loop Medtronic 780G system

  6. Time spent below range (≤ 54 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 6 months]

    Change in time spent below range (≤ 54 mg/dL) baseline to six months of closed-loop Medtronic 780G system

  7. Time spent above range (> 180 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 3 months]

    Change in time spent above range (> 180 mg/dL) baseline to three months of closed-loop Medtronic 780G system

  8. Time spent above range (> 180 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 6 months]

    Change in time spent above range (> 180 mg/dL) baseline to six months of closed-loop Medtronic 780G system

  9. Time spent above range (> 250 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 3 months]

    Change in time spent above range (> 250 mg/dL) baseline to three months of closed-loop Medtronic 780G system

  10. Time spent above range (> 250 mg/dL) as assessed from closed-loop Medtronic 780G system [0, 6 months]

    Delta time spent above range (> 250 mg/dL) baseline to six months of closed-loop Medtronic 780G system

  11. Quality of life - child as assessed by a questionnaire [0, 6 months]

    Change in quality of life - baseline to 6 months. A validated questionnaire, as cited in the Reference section. Min score 5, max score 100; the higher the score, the better quality of life.

  12. Quality of life - parent as assessed by a questionnaire [0, 6 months]

    Change in quality of life - baseline to 6 months. A validated questionnaire, as cited in the Reference section. Min score 37, max score 185; the higher the score, the better quality of life.

  13. Trait anxiety - child as assessed by a questionnaire [0, 6 months]

    Change in trait anxiety - baseline to 6 months. A validated questionnaire, as cited in the Reference section. Min score 20, max score 80; the higher the score, the higher the anxiety.

  14. Fear of hypoglycemia - child as assessed by a questionnaire [0, 6 months]

    Change in fear of hypoglycemia - baseline to 6 months. A validated questionnaire, as cited in the Reference section. Min score 25, max score 100; the higher the score, the higher the fear of hypoglycemia.

  15. Fear of hypoglycemia - parent as assessed by a questionnaire [0, 6 months]

    Change in fear of hypoglycemia - baseline to 6 months. A validated questionnaire, as cited in the Reference section. Min score 25, max score 100; the higher the score, the higher the fear of hypoglycemia.

  16. Diabetes management - child as assessed by a questionnaire [0, 6 months]

    Change in diabetes management - baseline to 6 months. A validated questionnaire, as cited in the Reference section. Min score 20, max score 100; the higher the score, the better the management of diabetes.

  17. Diabetes management - parent as assessed by a questionnaire [0, 6 months]

    Change in diabetes management - baseline to 6 months. A validated questionnaire, as cited in the Reference section. Min score 20, max score 100; the higher the score, the better the management of diabetes.

  18. Nutrition diaries as assessed by a dietician [0, 6 months]

    Change in carbohydrates grams - baseline to 6 months. Assessment of carbohydrates in grams by a certified pediatric nutritionist.

  19. Bioimpedance as measured in a bioimpedance measurement tool [0, 6 months]

    Change in bioimpedance measurements - baseline to 6 months

  20. Sleep quality as assessed by a questionnaire [0, 6 months]

    Change in sleep quality - baseline to 6 months, as assessed by a validated questionnaire, as cited in the Reference section.

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year to 21 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sheba Medical Center Ramat Gan Please Select Israel 5265601

Sponsors and Collaborators

  • Sheba Medical Center
  • Tel-Aviv Sourasky Medical Center
  • Assaf-Harofeh Medical Center
  • Maccabi Healthcare Services, Israel
  • Wolfson Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Noah Gruber, Pediatric endocrinologist, Sheba Medical Center
ClinicalTrials.gov Identifier:
NCT05908708
Other Study ID Numbers:
  • SHEBA-22-9609-NG-CTIL
First Posted:
Jun 18, 2023
Last Update Posted:
Jun 18, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Dr. Noah Gruber, Pediatric endocrinologist, Sheba Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 18, 2023