Improving diabetes Outcomes among youth with type 1 diabetes in Ahmedabad, India: Adoption of the 4T (Teamwork, Targets, Technology, and Tight Control) Program from Stanford, United States
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 53
- Locations
- 1
Study Overview
Brief Summary
Impact of the 4T (teamwork, target, technology, tight control) intervention on glycaemic outcomes among children and youth with type 1 diabetes in Ahmedabad, India
Abstract
Background: India has the highest estimated number of prevalent and incident cases of Type 1 Diabetes (T1D) in children and youth globally. Despite the benefits of intensive glucose control, translation into clinical practice remains limited.Objective: To assess HbA1c outcomes during the first year of diagnosis in children and youth with T1D by adopting the Stanford 4T model.
Hypothesis: Early use of Continuous Glucose Monitoring (CGM) within one year of diagnosis will significantly improve HbA1c levels and Increase Time-in-Range (TIR) compared to traditional monitoring.
Primary & Secondary Outcomes
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Primary Outcome: Optimal reduction of HbA1c (<7.5% from baseline) within 6 months of the study.
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Secondary Outcomes: * Reduction in hospitalizations due to Diabetic Ketoacidosis (DKA).
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Increased Time-in-Range (TIR) and reduced glycemic variability.
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Lowered frequency of moderate and severe hypoglycemia.
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Improved psychological measures (reduced diabetes-related distress) and high CGM satisfaction.
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4. Study Design & Methodology
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Type of Study: Randomized Controlled Trial (RCT).
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Allocation: 1:1 ratio using a computer-generated randomization sequence.
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Participants: Children and youth <18 years old diagnosed with T1D within one year of their clinical visit.
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Sample Size: 106 participants total (53 in the intervention arm, 53 in the control arm).
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Intervention: Use of the LinX CGM system (Bluetooth-enabled) paired with a phased education model involving virtual and face-to-face consultations.
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Control: Regular patient consultations and education every 3 months without virtual consultations or CGM.
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5. Recruitment & SettingThe study will be conducted at tertiary diabetes centers in Ahmedabad, India. Referral partnerships with public and private hospitals will be established to ensure rapid identification of new-onset cases.
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6. Ethical Considerations****Consent: Written informed consent will be obtained from parents (for those <13 years) and assent/consent from adolescents (14–18 years).
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Sponsors: International Society for Pediatric and Adolescent Diabetes (ISPAD) and Breakthrough T1D.
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- None
Eligibility Criteria
- Ages
- 5.00 Year(s) to 18.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Age 5 to 18 years Sex Both genders Diagnosed with within 1 year of clinical visit based on either antibody testing or C-peptide level.
Exclusion Criteria
- •Exclusion criteria are: 1.) Living with existing comorbidities or any complications.
- •2.) Not choosing CGM.
Investigators
Mahira Saiyed
Diacare
