{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Electronic+Screen+%2B+Education+%28Phase+1%29", "query": { "intervention": "Electronic Screen + Education (Phase 1)" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 5, "total_pages": 1, "next_page_url": null, "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-26T23:55:21.816Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT02841956", "title": "Reducing Duration of Untreated Psychosis Through Rapid Identification and Engagement", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Psychotic Disorders" ], "interventions": [ { "name": "Electronic Screen + Education (Phase 1)", "type": "OTHER" }, { "name": "Targeted Provider Education (Phase 1)", "type": "OTHER" }, { "name": "Community Mobile Engagement (Phase 2)", "type": "OTHER" }, { "name": "Clinic based Engagement (Phase 2)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, Davis", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "12 Years to 30 Years" }, "enrollment_count": 427, "start_date": "2014-09", "completion_date": "2020-03-13", "has_results": false, "last_update_posted_date": "2021-06-25", "last_synced_at": "2026-09-26T23:55:21.816Z", "location_count": 1, "location_summary": "Sacramento, California", "locations": [ { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02841956" }, { "nct_id": "NCT04996316", "title": "MammoScreen Breast Cancer Risk Assessment and Decision Aid for Breast Cancer Screening and Referrals", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Carcinoma" ], "interventions": [ { "name": "Electronic Health Record Review", "type": "OTHER" }, { "name": "Interview", "type": "OTHER" }, { "name": "Media Intervention", "type": "OTHER" }, { "name": "Survey Administration", "type": "OTHER" }, { "name": "Training and Education", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "OHSU Knight Cancer Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": "74 Years", "sex": "FEMALE", "summary": "40 Years to 74 Years · Female only" }, "enrollment_count": 1141, "start_date": "2022-09-07", "completion_date": "2026-08-31", "has_results": false, "last_update_posted_date": "2026-02-13", "last_synced_at": "2026-09-26T23:55:21.816Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT04996316" }, { "nct_id": "NCT05534412", "title": "A Practice-Based Intervention To Improve Care for a Diverse Population Of Women With Urinary Incontinence", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Urinary Incontinence" ], "interventions": [ { "name": "Academic Detailing", "type": "OTHER" }, { "name": "Electronic Clinical Decision Support", "type": "OTHER" }, { "name": "APP Co-management", "type": "OTHER" }, { "name": "Electronic Referral", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1600, "start_date": "2022-09-07", "completion_date": "2027-02-01", "has_results": false, "last_update_posted_date": "2026-03-13", "last_synced_at": "2026-09-26T23:55:21.816Z", "location_count": 4, "location_summary": "La Jolla, California • Los Angeles, California • Torrance, California", "locations": [ { "city": "La Jolla", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Torrance", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05534412" }, { "nct_id": "NCT05979714", "title": "The Cheeky Study: A Novel Delivery System for CAB-RPV LA", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infections" ], "interventions": [ { "name": "Patient-centered injection site", "type": "OTHER" }, { "name": "Patient-centered adherence support", "type": "BEHAVIORAL" }, { "name": "Provider education", "type": "OTHER" }, { "name": "Improved clinic communication strategies", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Public Health Foundation Enterprises, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 50, "start_date": "2023-05-31", "completion_date": "2024-12", "has_results": false, "last_update_posted_date": "2024-08-05", "last_synced_at": "2026-09-26T23:55:21.816Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05979714" }, { "nct_id": "NCT02963948", "title": "A Phased-Implementation Feasibility and Proof-of-Concept Study to Assess Incorporating the NIDA CTN Common Data Elements (CDEs) Into the Electronic Health Record (EHR) in Large Primary Care Settings (\"CDE-EHR-PC\" Study), Phase 3", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Substance Abuse" ], "interventions": [ { "name": "Meetings with implementation leader(s)", "type": "BEHAVIORAL" }, { "name": "the SAAS survey", "type": "BEHAVIORAL" }, { "name": "Patient surveys", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 113123, "start_date": "2018-02-28", "completion_date": "2019-09-09", "has_results": false, "last_update_posted_date": "2022-08-29", "last_synced_at": "2026-09-26T23:55:21.816Z", "location_count": 2, "location_summary": "Boston, Massachusetts • New York, New York", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02963948" } ] }