{ "data": { "asOf": "2026-10-30T22:25:17.505Z", "dedupMethod": "exact cross-registry identifier matching; probabilistic = review only", "byRegistry": { "clinicaltrials_gov": 1 }, "canonicalTrial": { "canonicalId": "NCT07612475", "title": "Universal Type 1 Diabetes Screening in Pediatrics", "scientificTitle": "Feasibility of Implementing Type One Diabetes Screening in Pediatric Clinics", "status": "recruiting", "studyType": "observational", "phase": [], "conditions": [ "Type 1 Diabetes (T1D)" ], "interventions": [ { "name": "Set of implementation strategies", "type": "BEHAVIORAL", "description": "This is an observational implementation study. The research team does not assign or deliver any clinical interventions. T1D screening orders and blood draws occur as part of routine care at clinician discretion, and the study observes EHR outcomes and collects surveys/interviews.\n\nThe research team will deliver a set of implementation strategies (clinician education, clinician ordering reminders, and facilitation) to all participating clinics to enable routine screening adoption. These are clinic-wide activities and are not research 'interventions' assigned to participants, and clinical decisions remain at clinician discretion. These strategies will not be randomly assigned." } ], "sponsor": { "name": "Northwestern University", "type": "OTHER" }, "locations": [ { "city": "Alexander City", "country": "United States", "facility": "Pediatric Associates of Alexander City" }, { "city": "Orlando", "country": "United States", "facility": "Pediatrics of Greater Orlando" }, { "city": "Birmingham", "country": "United States", "facility": "Bloom Pediatrics - Birmingham" }, { "city": "Bloomfield Township", "country": "United States", "facility": "Bloom Pediatrics - Bloomfield" }, { "city": "Detroit", "country": "United States", "facility": "Bloom Pediatrics - Detroit" }, { "city": "Southfield", "country": "United States", "facility": "Bloom Pediatrics - Southfield" }, { "city": "Bay Shore", "country": "United States", "facility": "RBK Pediatrics - Bay Shore" }, { "city": "Commack", "country": "United States", "facility": "RBK Pediatrics - Commack" } ], "outcomes": { "other": [], "primary": [ "Feasibility (Clinician Perspective)", "Acceptability (Parent Perspective)", "Acceptability (Clinician Perspective)", "Appropriateness (Parent Perspective)", "Appropriateness (Clinician Perspective)" ], "secondary": [ "Penetration of T1D Screening", "Reach of T1D Screening", "Clinical Documentation" ] }, "eligibility": { "sex": "ALL", "criteria": "Inclusion Criteria:\n\nChildren\n\n\\- Clinics will be encouraged to select screening ages or visits that align with international consensus statements for screening during early childhood, mid-childhood, and preadolescence and routine U.S. well-child visit schedules, and that minimize workflow disruption and maximize screening completion, such as visits that already include blood draws for other routine tests (e.g., lead screening at age 2). Children who have visits at their clinic's selected ages will be eligible to have their data extracted from the electronic health record (EHR)\n\nParents/Caregivers - All parents or legal guardians (hereafter, parents) who attended the well-child visit, who are eligible to have their child's EHR data extracted, and who are over age 18, will be eligible to complete the post-visit survey and interview.\n\nClinicians and Other Care Team Members\n\n* All pediatric primary care clinicians (i.e., physician \\[MD, DO\\], nurse practitioner, physician assistant) at participating clinics will be eligible to complete an interview.\n* All other care team members, including nurses, medical assistants, phlebotomists, and front desk staff at participating clinics will be eligible to complete an interview.\n\nExclusion Criteria:\n\n\\- Parents who have opted-out of survey recruitment at their clinic will not be eligible for the survey/interview.", "minimumAge": "1 Year", "healthyVolunteers": false }, "enrollment": { "type": "ESTIMATED", "count": 9500 }, "startDate": "2026-07-17", "completionDate": "2027-10-16", "lastUpdated": "2026-10-15T00:00:00.000Z", "firstPosted": "2026-05-28T00:00:00.000Z", "resultsAvailable": false, "sourceRegistries": [ "clinicaltrials_gov" ], "sourceUrls": [ "https://clinicaltrials.gov/study/NCT07612475" ] }, "identifiers": [ { "idType": "nct", "idValue": "NCT07612475", "declaredBy": "clinicaltrials_gov" } ], "sourceRecords": [ { "registry": "clinicaltrials_gov", "registryName": "ClinicalTrials.gov", "license": "public-domain", "sourceId": "NCT07612475", "sourceUrl": "https://clinicaltrials.gov/study/NCT07612475", "sourceStatus": "ENROLLING_BY_INVITATION", "retrievedAt": "2026-10-28T04:32:00.153Z", "payloadSha256": "da438dfab9e5e937559a6c38ed1f3ec0a13a0171aa9102c2f345d294b269b385", "piiRedacted": true } ], "citation": { "canonicalId": "NCT07612475", "sources": [ { "registry": "clinicaltrials_gov", "registryName": "ClinicalTrials.gov", "license": "public-domain", "sourceId": "NCT07612475", "verifyAt": "https://clinicaltrials.gov/study/NCT07612475", "retrievedAt": "2026-10-28T04:32:00.153Z", "payloadSha256": "da438dfab9e5e937559a6c38ed1f3ec0a13a0171aa9102c2f345d294b269b385", "text": "ClinicalTrials.gov, record NCT07612475 (https://clinicaltrials.gov/study/NCT07612475), retrieved 2026-10-28, licence: public-domain." } ], "crossRegistry": false, "dedupMethod": "exact cross-registry identifier matching; probabilistic = review only", "text": "Trial NCT07612475, registered in ClinicalTrials.gov, retrieved 2026-10-28. 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