{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Provider+Questionnaire&page=2", "query": { "intervention": "Provider Questionnaire", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Provider+Questionnaire&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-16T16:42:35.958Z", "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": "NCT04654117", "title": "Examining the Active Ingredients of Consultation of a Parent-mediated Intervention for Autism", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Autism Spectrum Disorder" ], "interventions": [ { "name": "Consultee-centered administrative consultation", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Michigan State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 41, "start_date": "2021-10-01", "completion_date": "2023-03-30", "has_results": true, "last_update_posted_date": "2025-04-03", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 1, "location_summary": "East Lansing, Michigan", "locations": [ { "city": "East Lansing", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04654117" }, { "nct_id": "NCT05734989", "title": "Improving Screening and Therapy for Hispanic/Latinx at Risk for CKD", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Type 2 Diabetes", "Chronic Kidney Diseases" ], "interventions": [ { "name": "BP", "type": "DIAGNOSTIC_TEST" }, { "name": "HbA1c", "type": "DIAGNOSTIC_TEST" }, { "name": "PCP Guidelines for Screening and Monitoring Hispanic/Latinx patients for CKD", "type": "BEHAVIORAL" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "BEHAVIORAL" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 248, "start_date": "2023-05-18", "completion_date": "2025-04-04", "has_results": true, "last_update_posted_date": "2026-04-24", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05734989" }, { "nct_id": "NCT06737380", "title": "UC-MSC Cell Therapy Study for Systemic Lupus Erythematosus (SLE) Patients", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "SLE", "Lupus", "Systemic Lupus Erthematosus", "Systemic Lupus Erythematosus", "Systemic Lupus Erythematosus (SLE)" ], "interventions": [ { "name": "Physical examination", "type": "DIAGNOSTIC_TEST" }, { "name": "Electrocardiogram", "type": "DIAGNOSTIC_TEST" }, { "name": "SF-36 questionnaire", "type": "OTHER" }, { "name": "Clinical laboratory evaluations - Serology", "type": "DIAGNOSTIC_TEST" }, { "name": "Clinical laboratory evaluations - Biochemistry", "type": "DIAGNOSTIC_TEST" }, { "name": "Clinical laboratory evaluations - Hematology", "type": "DIAGNOSTIC_TEST" }, { "name": "Pregnancy Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Urinalysis", "type": "DIAGNOSTIC_TEST" }, { "name": "SLE activity evaluation", "type": "DIAGNOSTIC_TEST" }, { "name": "SLE biomarker profiling", "type": "DIAGNOSTIC_TEST" }, { "name": "Cytokines and chemokine profiling", "type": "DIAGNOSTIC_TEST" }, { "name": "single dose of UC-MSCs", "type": "BIOLOGICAL" }, { "name": "PROMIS instruments", "type": "OTHER" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER", "BIOLOGICAL" ], "sponsor": "LiveKidney.Bio", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 10, "start_date": "2025-01-07", "completion_date": "2026-07", "has_results": false, "last_update_posted_date": "2025-09-11", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06737380" }, { "nct_id": "NCT05341726", "title": "BREATHE: An Efficacy-implementation Trial Among Black Adults With Uncontrolled Asthma", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Asthma" ], "interventions": [ { "name": "BREATHE Intervention", "type": "BEHAVIORAL" }, { "name": "Control Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 400, "start_date": "2023-01-19", "completion_date": "2026-07", "has_results": false, "last_update_posted_date": "2026-01-30", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 2, "location_summary": "Beacon, New York • Brooklyn, New York", "locations": [ { "city": "Beacon", "state": "New York" }, { "city": "Brooklyn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05341726" }, { "nct_id": "NCT05368389", "title": "Observational Study of Wearable Health Monitoring Device", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Weight Loss" ], "interventions": [ { "name": "Healthdot attachment", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "22 Years to 60 Years" }, "enrollment_count": 33, "start_date": "2022-11-03", "completion_date": "2023-06-21", "has_results": false, "last_update_posted_date": "2024-03-28", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05368389" }, { "nct_id": "NCT03018912", "title": "Validating the Use of a Subjectively Reported Sleep Vital Sign", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obstructive Sleep Apnea (OSA)", "Insomnia", "Restless Leg Syndrome (RLS)", "Hypersomnia Type; Sleep Disorder", "Shift Work Sleep Disorders" ], "interventions": [ { "name": "Sleep VS", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Kaiser Permanente", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1260, "start_date": "2018-10-22", "completion_date": "2019-06-01", "has_results": false, "last_update_posted_date": "2026-07-21", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 1, "location_summary": "Fontana, California", "locations": [ { "city": "Fontana", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03018912" }, { "nct_id": "NCT02797054", "title": "Educational Intervention to Improve HPV Vaccination Decision Quality", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HPV Vaccination Decision Quality" ], "interventions": [ { "name": "Tailored educational materials", "type": "BEHAVIORAL" }, { "name": "Untailored educational materials", "type": "BEHAVIORAL" }, { "name": "Usual care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 1205, "start_date": "2014-06", "completion_date": "2016-06", "has_results": true, "last_update_posted_date": "2018-09-21", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT02797054" }, { "nct_id": "NCT07270666", "title": "ctDNA Testing to Inform Standard-of-Care Treatment Decisions in People With Endometrial Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Endometrial Cancer" ], "interventions": [ { "name": "ctDNA Testing", "type": "GENETIC" }, { "name": "Blood draw", "type": "OTHER" }, { "name": "Surveys", "type": "OTHER" }, { "name": "Semi-structured interviews", "type": "OTHER" } ], "intervention_types": [ "GENETIC", "OTHER" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 30, "start_date": "2025-11-25", "completion_date": "2027-11", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 7, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Montvale, New Jersey + 4 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07270666" }, { "nct_id": "NCT07723495", "title": "Symptom Management to Improve Completion of Patient-reported Outcome Measures", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Malignant Solid Neoplasm", "Malignant Head and Neck Neoplasm", "Malignant Lung Neoplasm" ], "interventions": [ { "name": "Monitoring of PROMIS symptoms and physical function", "type": "BEHAVIORAL" }, { "name": "Monitoring of additional symptoms and symptom self-management", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Henry Ford Health System", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 78, "start_date": "2027-10-01", "completion_date": "2031-09-01", "has_results": false, "last_update_posted_date": "2026-07-29", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT07723495" }, { "nct_id": "NCT05594693", "title": "Integrative Health Interventions in Symptom Management of Pediatric Patients", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cancer", "Pediatric Cancer" ], "interventions": [ { "name": "Questionnaire", "type": "OTHER" }, { "name": "Physical Exam", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Days", "maximum_age": "30 Years", "sex": "ALL", "summary": "30 Days to 30 Years" }, "enrollment_count": 100, "start_date": "2022-06-16", "completion_date": "2024-02-26", "has_results": false, "last_update_posted_date": "2026-01-16", "last_synced_at": "2026-09-16T16:42:35.958Z", "location_count": 3, "location_summary": "Aurora, Colorado • Portland, Oregon", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Aurora", "state": "Colorado" }, { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT05594693" } ] }