{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=No+screening+testing+strategy", "query": { "intervention": "No screening testing strategy" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 16, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=No+screening+testing+strategy&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-04T00:11:23.935Z", "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": "NCT01377857", "title": "HIV Screening Take-up: Evaluating Incentives and Opt-out Strategies", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV" ], "interventions": [ { "name": "Monetary Incentive", "type": "BEHAVIORAL" }, { "name": "Questionnaire Timing", "type": "BEHAVIORAL" }, { "name": "HIV Test Offering", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "13 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "13 Years to 64 Years" }, "enrollment_count": 8572, "start_date": "2011-05", "completion_date": "2013-12", "has_results": false, "last_update_posted_date": "2015-05-14", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01377857" }, { "nct_id": "NCT06441955", "title": "Covid-19 Long Haul Preventative and Health Promotion Care Clinical Trial Acceleration Program.", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "COVID-19, Long Haul" ], "interventions": [ { "name": "Ritonavir-Boosted Nirmatrelvir (Paxlovid)", "type": "DRUG" }, { "name": "Physiological Evaluation", "type": "DIAGNOSTIC_TEST" }, { "name": "Moderna COVID-19 Vaccine", "type": "BIOLOGICAL" }, { "name": "Biopsychological", "type": "BEHAVIORAL" }, { "name": "Behavioral (e.g., Psychotherapy, Lifestyle Counseling)", "type": "BEHAVIORAL" }, { "name": "Genetic (including gene transfer, stem cell and recombinant DNA)", "type": "GENETIC" }, { "name": "Multidisciplinary approach", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "DRUG", "DIAGNOSTIC_TEST", "BIOLOGICAL", "BEHAVIORAL", "GENETIC", "COMBINATION_PRODUCT" ], "sponsor": "Well- Konnect Healthcare Services and Research Firm", "sponsor_class": "NETWORK", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 100, "start_date": "2024-03-01", "completion_date": "2030-09-30", "has_results": false, "last_update_posted_date": "2024-11-27", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT06441955" }, { "nct_id": "NCT04875520", "title": "Assessing Testing Strategies for Safe Return to K-12 Schools in an Underserved Population", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Covid19" ], "interventions": [ { "name": "Screening testing strategy", "type": "OTHER" }, { "name": "No screening testing strategy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "0 Years", "maximum_age": null, "sex": "ALL", "summary": "0 Years and older" }, "enrollment_count": 1390, "start_date": "2021-05-07", "completion_date": "2023-12-31", "has_results": true, "last_update_posted_date": "2026-06-29", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 5, "location_summary": "Hazelwood, Missouri • Jennings, Missouri • Saint Ann, Missouri + 2 more", "locations": [ { "city": "Hazelwood", "state": "Missouri" }, { "city": "Jennings", "state": "Missouri" }, { "city": "Saint Ann", "state": "Missouri" }, { "city": "St Louis", "state": "Missouri" }, { "city": "University City", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04875520" }, { "nct_id": "NCT02121548", "title": "Using CHWs and HPV Home Tests to Increase Cervical Cancer Screening in Minority Populations", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cervical Cancer" ], "interventions": [ { "name": "CHW Outreach and HPV Self-sampling", "type": "BEHAVIORAL" }, { "name": "CHW Outreach", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "30 Years to 65 Years · Female only" }, "enrollment_count": 601, "start_date": "2011-10-10", "completion_date": "2015-02-17", "has_results": false, "last_update_posted_date": "2018-10-17", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02121548" }, { "nct_id": "NCT03930524", "title": "Adaptive Preventive Intervention for College Alcohol Use", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "College Student Drinking" ], "interventions": [ { "name": "Personalized Normative Feedback (PNF)", "type": "BEHAVIORAL" }, { "name": "Self-Monitoring (SM)", "type": "BEHAVIORAL" }, { "name": "Web-BASICS", "type": "BEHAVIORAL" }, { "name": "Health Promotion Consultation", "type": "BEHAVIORAL" }, { "name": "M-Bridge Online Health Coach", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "18 Years to 21 Years" }, "enrollment_count": 891, "start_date": "2019-07-31", "completion_date": "2022-08-01", "has_results": true, "last_update_posted_date": "2023-04-12", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03930524" }, { "nct_id": "NCT02353117", "title": "Preventing Congenital Syphilis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Congenital Syphilis" ], "interventions": [ { "name": "Congenital Syphilis Intervention Group", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Tulane University School of Public Health and Tropical Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "13 Years", "maximum_age": null, "sex": "FEMALE", "summary": "13 Years and older · Female only" }, "enrollment_count": 60386, "start_date": "2016-01-11", "completion_date": "2018-02-28", "has_results": false, "last_update_posted_date": "2018-04-26", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 1, "location_summary": "New Orleans, Louisiana", "locations": [ { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT02353117" }, { "nct_id": "NCT01710215", "title": "Comparative Effectiveness of FIT, Colonoscopy, & Usual Care Screening Strategies", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colorectal Cancer" ], "interventions": [ { "name": "FIT Screening Strategy", "type": "OTHER" }, { "name": "Colon Screening Strategy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Texas Southwestern Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "50 Years to 64 Years" }, "enrollment_count": 5999, "start_date": "2013-04", "completion_date": "2016-07", "has_results": false, "last_update_posted_date": "2018-04-26", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01710215" }, { "nct_id": "NCT02765672", "title": "Effectiveness of a Driving Intervention on Safe Community Mobility for Returning Combat Veterans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Traumatic Brain Injury (TBI)", "Post Traumatic Stress Disorder (PTSD)" ], "interventions": [ { "name": "Driving Behavior Interview", "type": "BEHAVIORAL" }, { "name": "Clinical Driving Assessment", "type": "OTHER" }, { "name": "Propensity for Angry Driving Scale", "type": "BEHAVIORAL" }, { "name": "Community Integration Questionnaire", "type": "BEHAVIORAL" }, { "name": "Satisfaction with Life", "type": "BEHAVIORAL" }, { "name": "Fitness-to-Drive Screening Measure (FTDS)", "type": "BEHAVIORAL" }, { "name": "Simulated Driving Evaluation", "type": "PROCEDURE" }, { "name": "Driving Safety Education", "type": "PROCEDURE" }, { "name": "Occupational Therapy Driving Intervention (OT-DI)", "type": "PROCEDURE" }, { "name": "On-road driving test", "type": "PROCEDURE" }, { "name": "Driving triggers evaluation", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "PROCEDURE" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 58, "start_date": "2016-12", "completion_date": "2023-12-20", "has_results": false, "last_update_posted_date": "2024-01-19", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 2, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02765672" }, { "nct_id": "NCT05836090", "title": "Family Spirit Strengths", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depressive Symptoms", "Anxiety Disorders and Symptoms", "Substance Use", "Mental Health Issue" ], "interventions": [ { "name": "Family Spirit Strengths (FSS)", "type": "BEHAVIORAL" }, { "name": "Family Spirit Nurture", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Johns Hopkins Bloomberg School of Public Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": null, "sex": "FEMALE", "summary": "14 Years and older · Female only" }, "enrollment_count": 188, "start_date": "2023-04-20", "completion_date": "2028-06-30", "has_results": false, "last_update_posted_date": "2026-04-13", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 3, "location_summary": "Chinle, Arizona • Pokagon, Michigan • Shiprock, New Mexico", "locations": [ { "city": "Chinle", "state": "Arizona" }, { "city": "Pokagon", "state": "Michigan" }, { "city": "Shiprock", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT05836090" }, { "nct_id": "NCT04397744", "title": "Unidas Por Vida y Salud: Increasing Breast and Cervical Cancer Screening in El Paso", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Cervical Cancer" ], "interventions": [ { "name": "Unidas por Vida y Salud prevention program", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "64 Years", "sex": "FEMALE", "summary": "21 Years to 64 Years · Female only" }, "enrollment_count": 660, "start_date": "2015-01-16", "completion_date": "2017-10-17", "has_results": false, "last_update_posted_date": "2020-05-21", "last_synced_at": "2026-09-04T00:11:23.935Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04397744" } ] }