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Enrolling by invitation No phase listed Observational

Universal Type 1 Diabetes Screening in Pediatrics

ClinicalTrials.gov ID: NCT07612475

Public ClinicalTrials.gov record NCT07612475. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 16, 2026, 1:17 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Feasibility of Implementing Type One Diabetes Screening in Pediatric Clinics

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study examines how population-based screening for type 1 diabetes (T1D) using islet autoantibodies (i.e., immune system proteins) can be incorporated into pediatric primary care during routine well-child visits. The project evaluates whether this screening approach, supported by the study's implementation approach, is feasible, acceptable, and appropriate for clinicians, parents, and other key constituent groups. The study also explores how often clinicians order the test, how often patients complete it, and how often clinicians document stages of early-stage T1D in the patients' electronic health records. Insights from parents, clinicians, other care team members, pediatric endocrinologists, and national and regional experts will inform future scale-up efforts and practical strategies to improve early detection of T1D in pediatric practices across the United States.

Study identification

NCT ID
NCT07612475
Recruitment status
Enrolling by invitation
Study type
Observational
Phase
Not listed
Lead sponsor
Northwestern University
Other
Enrollment
9,500 participants

Conditions and interventions

Interventions

Behavioral

Eligibility (public fields only)

Age range
1 Year and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 17, 2026 (Actual)
Primary completion
Oct 16, 2027 (Estimated)
Completion
Oct 16, 2027 (Estimated)
Last update posted
Oct 15, 2026

2026 – 2027

United States locations

U.S. sites
8
U.S. states
4
U.S. cities
8
Facility City State ZIP Site status
Pediatric Associates of Alexander City Alexander City Alabama 35010 —
Pediatrics of Greater Orlando Orlando Florida 32835 —
Bloom Pediatrics - Birmingham Birmingham Michigan 48009 —
Bloom Pediatrics - Bloomfield Bloomfield Township Michigan 48302 —
Bloom Pediatrics - Detroit Detroit Michigan 48201 —
Bloom Pediatrics - Southfield Southfield Michigan 48034 —
RBK Pediatrics - Bay Shore Bay Shore New York 11706 —
RBK Pediatrics - Commack Commack New York 11725 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07612475, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 15, 2026 · Synced Oct 16, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07612475 live on ClinicalTrials.gov.

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