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Type 1 DiabetesNCT04807374

Hybrid Closed Loop in High Risk Youth With Type 1 Diabetes

A study of Type 1 Diabetes, run by Children's National Research Institute at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The use of insulin pumps and continuous glucose monitors for Type 1 diabetes (T1D) has been shown to improve glycemic control while also decreasing the risk for acute and chronic complications. Read more about this study

Who is it for?
Ages 6 to 21 years
Conditions the study is for
Type 1 Diabetes
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
1 siteUnited States
Study dates
1 Jun 2021to 22 Jun 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 21 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Patients clinically diagnosed with T1D managed with insulin for at least 1 year
  • Black race
  • Public healthcare insurance
  • Male or female ages ≥ 6 and < 21 years
  • Not currently using insulin pump therapy
  • Poorly controlled T1D: one A1c value ≥ 10% in the preceding two years and a second A1c value ≥ 10% at enrollment
Show all 13Show fewer
  • Investigators and primary clinical endocrine clinician have confidence that the participant can successfully operate all study devices and is capable of adhering to the protocol
  • Living with one or more parent/legal guardian/ friend (for adults only) knowledgeable about emergency procedures for severe hypoglycemia and able to contact the participant in case of an emergency.
  • Total daily insulin dose of at least 10 units per day based on FDA approval for Control IQ
  • For females, not currently known to be pregnant If female and sexually active, must agree to use a form of contraception to prevent pregnancy while a participant in the study. A negative serum or urine pregnancy test will be required for all females of child-bearing potential at study entry and can be repeated as necessary in case of clinical concern. Participants who become pregnant will be discontinued from the study. Also, participants who during the study develop and express the intention to become pregnant within the timespan of the study will be discontinued.
  • Not currently using and willingness not to start any non-insulin glucose-lowering agent during the course of the trial
  • Fluent in English as the Control IQ technology is currently available only in English
  • Willing to adhere to the study regimen

Who cannot join

  • Concurrent use of any non-insulin diabetes medications
  • More than 3 episodes of DKA in the year prior to enrollment
  • Major illnesses other than T1D
  • Significant cognitive limitations and major psychiatric disorders
  • A condition, which in the opinion of the investigator or designee, would put the participant or study at risk
  • Participation in another pharmaceutical or device trial at the time of enrollment or during the study
  • Having immediate family members employed by Tandem Diabetes Care, Inc., TypeZero Technologies, LLC, Dexcom, Inc. or having a direct supervisor at place of employment who is also directly involved in conducting the clinical trial (as a study investigator, coordinator, etc.); or having a first-degree relative who is directly involved in conducting the clinical trial

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Children's National

    Washington D.C., District of Columbia, 20010

Other trials in United States

About this study

Official title: Use of a Hybrid Closed Loop Insulin Delivery System in a High Risk Type 1 Diabetes Population

The use of insulin pumps and continuous glucose monitors for Type 1 diabetes (T1D) has been shown to improve glycemic control while also decreasing the risk for acute and chronic complications. Unfortunately, there are vast disparities in access to this technology; non-Hispanic black youth with public healthcare insurance are the least likely to have access to these technologies. We propose to conduct a non-randomized interrupted time series study to assess the impact of hybrid closed loop (HCL) insulin delivery in underserved youths with poorly controlled T1D. Patients will complete standard diabetes education before beginning to use this technology and will be followed for 6-months after starting HCL to assess its impact on glycemic control and health-related quality of life.

Read the detailed description

T1D is among the most common chronic childhood illness, affecting an estimated 1 in 400 American children.2 The care of children and adolescents with type 1 diabetes aims to optimize glycemic control to prevent acute and chronic complications of both hypoglycemia and hyperglycemia.

CGMs are minimally invasive devices that use a subcutaneous sensor to report and record changes in interstitial glucose values every 5 minutes to 15 minutes.6 This technology can alert patients to hypoglycemia and hyperglycemia and also allows them to make diabetes treatment decisions without the need for a confirmatory fingerstick blood glucose level. Improvements in the accuracy and usability of CGM, better insurance coverage, and greater acceptance by both clinicians and patients have led to dramatic increases in the use of this technology over the past decade.1,7-15 In 2011, just 6% of all patients in the United States Type 1 Diabetes Exchange (T1DX) registry were using CGM as compared to 27% in the period from 2016-2018.1 The use of CGM therapy has been associated with decreased hypoglycemia and severe hypoglycemia,16,17 improvements in A1c,1 reduced fear of hypoglycemia,18 and improved diabetes treatment satisfaction.19 Insulin pump therapy provides a continuous subcutaneous infusion of rapid acting insulin that allows for more physiologic insulin delivery as compared to multiple daily injection therapy. The use of insulin pump therapy in children with T1D has been associated with improved glycemic control, decreased rates of DKA, lower risk for microvascular complications, as well as psychosocial benefits.

Recently, input from CGM has been used to guide automated insulin delivery through insulin pumps in what is referred to as HCL insulin delivery. The Control IQ algorithm developed by Tandem Diabetes Care, Inc. uses a Dexcom G6 to adjust insulin delivery according to predicted glucose levels in 30 minutes to maximize TIR. Control IQ was FDA approved for patients with T1D ≥ 14 years of age in December 2019 and for patients ≥ 6 years of age in June 2020. A 6-month randomized controlled study of the Control IQ algorithm showed improvements in mean glucose, TIR, time in hypoglycemia, and time in hyperglycemia.25 Although Control IQ was shown to have positive impacts on glycemic control, its impact on those in poor glycemic control remains largely unknown. Prior studies included only a selected population: 86% of participants were white, 86% of participants had at least a bachelor's degree, 62% had an annual household income >$100,000, and the average A1c on enrollment was 7.4 ± 1.0%.

The increasing use of insulin pumps and continuous glucose monitors (CGM) among people with Type 1 diabetes (T1D) has been associated with worsening already existing healthcare disparities among people of different races, ethnicities, and socioeconomic statuses. Studies have shown that CGM use is more likely among participants with higher household incomes, greater levels of parental education, and those with private healthcare insurance.8 The disparities in access to these technologies persist even after controlling for these factors, which raises concern for clinician bias in prescribing these technologies despite evidence from an RCT that CGM use is equally beneficial for children of different racial and ethnic groups.26 There has been an ongoing push to better understand the various factors contributing to these disparities in access to diabetes technologies.27 Evidence that technology use varies according to geographic location speaks to the role of provider preference as well as patient socioeconomic status.28 The association between black race and higher rates of DKA and mortality in patients with T1D <25 years of age may impact provider insulin pump prescribing practices.29 While ongoing work is necessary to better understand factors impacting prescribing practices, the addition of data supporting the effectiveness of HCL therapy without higher rates of DKA in underserved patients can only help to strengthen this argument.

We aim to explore the effect of HCL insulin therapy with the Control IQ system on glycemic control as measured by time in range (TIR) in underserved youths ≥ 6 to < 21 years of age with poorly controlled T1D. For the purposes of this study, because of the lowest rates of diabetes technology use in this group, underserved patients will be defined as: non-Hispanic black with public healthcare insurance being managed with insulin regimens using either NPH or sliding scales. Poorly controlled T1D will be defined as: at least two A1c values ≥10% in the preceding year. We have specifically chosen these inclusion criteria for the purposes of this pilot study because we wish to show the effectiveness of using these technologies in patients who are the least likely to have access to diabetes technologies.

Conditions
Type 1 Diabetes
Being tested
Control IQ
Keywords
hybrid closed loop insulin delivery, healthcare disparities, diabetes technology
Medical subject headings
Diabetes Mellitus, Type 1

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Control IQDevice

    We aim to conduct a non-randomized prospective interrupted time series pilot study to investigate the effect of HCL insulin delivery on glycemic control in underserved adolescents with poorly controlled T1D.

Study groups in NCT04807374
Study groupRoleWhat they receive
Single arm- HCL TherapyExperimentalSingle arm study with all participants being treated with HCL for 6 months given the non-randomized interrupted time series study design.
Receives: Device: Control IQ

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in CGM Time in Range (TIR)

    To explore the effect of HCL insulin therapy with the Control IQ system on glycemic control as measured by time in range (TIR) in underserved youth with poorly controlled T1D.

    Measured: 6 months

Secondary outcomes (20)
  1. Changes in mean CGM glucose

    Measured: 6 months

  2. Changes in glycemic management indicator (GMI)

    Measured: 6 months

  3. Changes in coefficient of variation of mean glucose

    Measured: 6 months

  4. Changes in CGM time in hypoglycemia (<70 mg/dL)

    Measured: 6 months

  5. Changes in CGM time in hyperglycemia (>180 mg/dL)

    Measured: 6 months

  6. Glycemic control as measured by hemoglobin A1c

    Measured: 6 months

  7. Incidence of diabetic ketoacidosis (DKA)

    Measured: 6 months

  8. Incidence of severe hypoglycemia

    Measured: 6 months

  9. Incidence of emergency department visits and hospital admissions

    Measured: 6 months

  10. Changes in youth perceptions of diabetes-specific quality of life

    As measured by Type 1 Diabetes and Life (T1DAL)

    Measured: 6 months

  11. Changes in youth perceptions of diabetes distress

    As measured by Problem Areas in Diabetes (PAID)

    Measured: 6 months

  12. Changes in youth perceptions of automated insulin delivery systems

    As measured by INsulin Dosing Systems: Perceptions, Ideas, Reflections, and Expectations (INSPIRE)

    Measured: 6 months

  13. Changes in youth perceptions diabetes self-management

    As measured by Diabetes Management Questionnaire (DMQ)

    Measured: 6 months

  14. Changes in youth attitudes about diabetes technologies

    As measured by Diabetes Technology Attitudes Survey (DTAS)

    Measured: 6 months

  15. Changes in parental perceptions of the youth's diabetes-specific quality of life

    As measured by Type 1 Diabetes and Life (T1DAL) for Parents of People with Type 1 Diabetes

    Measured: 6 months

  16. Changes in parental perceptions of the youth's diabetes distress

    As measured by Parent Problem Areas in Diabetes (PAID)

    Measured: 6 months

  17. Changes in parental perceptions of the youth's perceptions of automated insulin delivery systems

    As measured by INsulin Dosing Systems: Perceptions, Ideas, Reflections, and Expectations (INSPIRE)

    Measured: 6 months

  18. Changes in parental perceptions of the youth's diabetes management

    As measured by Diabetes Management Questionnaire (DMQ) for parents

    Measured: 6 months

  19. Changes in parental perceptions of the youth's attitudes about diabetes technologies

    As measured by Parent Diabetes Technology Attitudes Survey (DTAS)

    Measured: 6 months

  20. Semi-structured interviews with youth and parents exploring the overall experience and barriers to expanding access to hybrid closed loop technology

    Measured: Post-Intervention at 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Mar 2021
  2. Study start1 Jun 2021
  3. Primary completion22 Mar 2023
  4. Study completion22 Jun 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
non-randomized interrupted time series
Masking
None (open label)
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04807374
Sponsor's protocol ID
Pro00013963
Status last verified
Aug 2023
First submitted
11 Mar 2021
Last updated
29 Aug 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Publications

  • Marks BE, Grundman JB, Meighan S, Monaghan M, Streisand R, Perkins A. Hybrid Closed Loop Systems Improve Glycemic Control and Quality of Life in Historically Minoritized Youth with Diabetes. Diabetes Technol Ther. 2024 Mar;26(3):167-175. doi: 10.1089/dia.2023.0450.

    PubMed 38444316

Questions about this trial

What is this clinical trial studying?

A study of Type 1 Diabetes, run by Children's National Research Institute at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Aug 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in CGM Time in Range (TIR) (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04807374, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Aug 2023.

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