Strategies to Enhance New CGM Use in Early Childhood (SENCE)

Completed · Not applicable

Conditions studied: Type 1 Diabetes Mellitus

In brief

The primary objective of this study is to compare the efficacy and safety of CGM alone and CGM combined with a family behavioral intervention with a control group using home blood glucose monitoring (BGM) alone.

Key facts

Study ID

NCT02912728

Run by

Jaeb Center for Health Research

People needed

143

Starts

2017-01-30

Expected to finish

2019-06-30

Last updated by the study team

2020-10-05

Who can join

Age: 2 and older, up to 7. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Clinical diagnosis of insulin dependent presumed autoimmune type 1 diabetes by the investigator
• Age 2-<8 years at consent
• Diabetes duration ≥ 6 months
• Total daily insulin ≥ 0.3 units per kg per day
• HbA1c 7.0% to <10.0% (Point of care device or local lab measured within 30 days of screening visit used to assess eligibility)
• No use of unblinded personal CGM, outside of a research study, as part of real-time diabetes management in the last 30 days
• Insulin regimen involves either use of a consistent insulin regimen with an insulin pump in the last 3 months or at least 3 multiple daily injections of basal and bolus (meal time) analogue insulin in the last 3 months (e.g. no change from injections to pump or vice versa in the last 3 months), with no plans to switch the modality of insulin administration during the next 6 months (e.g., injection user switching to a pump, pump user switching to injections).
• Perform at least 3 blood glucose meter checks per day from self-report at screening and meter download during blinded CGM run in
• Not currently using and no plans to begin non-insulin medication for blood glucose lowering during the course of the study
• Parent or guardian comprehend written and spoken English (This requirement is due to the fact that the questionnaires to be used as outcome measures do not have validated versions in other languages, and interventions will be delivered in English only for the RCT to ensure standardization/fidelity checks across sites).
• Parent understands the study protocol and agrees to it
• No expectation that participant/parent will be moving out of the area of the clinical center during the next 12 months, unless the move will be to an area served by another study center.

You may not qualify if…

• Use of unblinded personal CGM, outside of a research study, as part of real-time diabetes management in the last 30 days
• Unable to use CGM device for minimum number of hours during blinded run-in period or skin reaction from adhesive that would preclude participation in the randomized trial
• The presence of a significant medical disorder or use of a medication such as oral/inhaled glucocorticoids that in the judgment of the investigator will affect the wearing of the sensors or the completion of any aspect of the protocol.
• More than 1 episode of SH or DKA in the past 6 months (not including DKA at time of dx).
• The presence of any of the following diseases:
• Asthma if treated with systemic or daily inhaled corticosteroids in the last 6 months (Intermittent treatment with inhaled corticosteroids does not exclude subjects from enrollment)
• Cystic fibrosis (Adequately treated thyroid disease and celiac disease do not exclude subjects from enrollment)
• Inpatient psychiatric treatment in the past 6 months for either child participant or the primary care giver
• Need for use of acetaminophen or acetaminophen-containing products on a regular basis during the 6 months of the trial
• Participation of parent or child in a diabetes related intervention study in past 6 weeks.
• Any medical, psychological or social situation where per investigator discretion it may be difficult for family or child to participate fully in the intervention
• Another member of the same household is participating in this study.

Where it is running

• Indiana — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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