{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=After+Initial+Treatment+Decision&page=3", "query": { "intervention": "After Initial Treatment Decision", "page": 3 }, "page_size": 10 }, "pagination": { "page": 3, "page_size": 10, "total_count": 298, "total_pages": 30, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=After+Initial+Treatment+Decision&page=4&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=After+Initial+Treatment+Decision&page=2&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-05T03:36:11.156Z", "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": "NCT06105957", "title": "Optimal Digital Weight Loss Treatment for Rural Individuals", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Overweight and Obesity" ], "interventions": [ { "name": "Core", "type": "BEHAVIORAL" }, { "name": "Facilitated Weekly Group Sessions", "type": "BEHAVIORAL" }, { "name": "Counselor Crafted Feedback", "type": "BEHAVIORAL" }, { "name": "Individual Coaching Calls", "type": "BEHAVIORAL" }, { "name": "Pre-Scripted Feedback", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 616, "start_date": "2024-01-03", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2025-12-23", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 1, "location_summary": "Columbia, South Carolina", "locations": [ { "city": "Columbia", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06105957" }, { "nct_id": "NCT07446777", "title": "FAST-M: Prolonged Overnight Fasting and Mediterranean Dietary Intervention for Patients With Multiple Myeloma or Its Precursor Disease", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Multiple Myeloma", "Monoclonal Gammopathy of Undetermined Significance", "Smoldering Multiple Myeloma" ], "interventions": [ { "name": "Health Coaching", "type": "BEHAVIORAL" }, { "name": "Prolonged Overnight Fasting (POF)", "type": "BEHAVIORAL" }, { "name": "Mediterranean Diet", "type": "BEHAVIORAL" }, { "name": "Supportive Materials", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2026-04-07", "completion_date": "2029-04-30", "has_results": false, "last_update_posted_date": "2026-05-01", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07446777" }, { "nct_id": "NCT02780739", "title": "INSIGHT, A Comprehensive, Multidisciplinary Brain Training System", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cognitive Ability, General" ], "interventions": [ { "name": "Cognitive Training - 48 sessions", "type": "BEHAVIORAL" }, { "name": "Fitness", "type": "BEHAVIORAL" }, { "name": "Active Control", "type": "BEHAVIORAL" }, { "name": "active tDCS", "type": "DEVICE" }, { "name": "sham tDCS", "type": "DEVICE" }, { "name": "Cognitive Training - 20 sessions", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE" ], "sponsor": "University of Illinois at Urbana-Champaign", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "44 Years", "sex": "ALL", "summary": "18 Years to 44 Years" }, "enrollment_count": 521, "start_date": "2014-03", "completion_date": "2014-11", "has_results": false, "last_update_posted_date": "2016-05-23", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 1, "location_summary": "Urbana, Illinois", "locations": [ { "city": "Urbana", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02780739" }, { "nct_id": "NCT06075797", "title": "The PediQUEST Response to Pain Of Children With Neurologic Disability Pilot Randomized Controlled Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cerebral Palsy Infantile", "Disabilities Multiple", "Pain" ], "interventions": [ { "name": "PediQUEST ResPOND", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": null, "sex": "ALL", "summary": "1 Year and older" }, "enrollment_count": 54, "start_date": "2024-05-08", "completion_date": "2025-07-31", "has_results": false, "last_update_posted_date": "2026-01-21", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 3, "location_summary": "Birmingham, Alabama • Boston, Massachusetts", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06075797" }, { "nct_id": "NCT06458660", "title": "LinkPositively+ A Mobile Health App Delivered Intervention to Improve HIV Care Outcomes Among Black Women Affected by Mental Health and Violence", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV/AIDS", "Mental Health Issue" ], "interventions": [ { "name": "LPP+: Mindfulness Meditation Delivered", "type": "BEHAVIORAL" }, { "name": "LP", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Guiding Right, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2024-04-12", "completion_date": "2025-01-15", "has_results": false, "last_update_posted_date": "2024-06-13", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 3, "location_summary": "Oklahoma City, Oklahoma • Tulsa, Oklahoma", "locations": [ { "city": "Oklahoma City", "state": "Oklahoma" }, { "city": "Oklahoma City", "state": "Oklahoma" }, { "city": "Tulsa", "state": "Oklahoma" } ], "official_url": "https://clinicaltrials.gov/study/NCT06458660" }, { "nct_id": "NCT02954536", "title": "Phase II Trial of Pembrolizumab With Trastuzumab and Chemotherapy in Advanced HER2 Positive Esophagogastric (EG) Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Esophageal Cancer", "Gastric Cancer" ], "interventions": [ { "name": "pembrolizumab", "type": "DRUG" }, { "name": "trastuzumab", "type": "DRUG" }, { "name": "capecitabine", "type": "DRUG" }, { "name": "cisplatin", "type": "DRUG" }, { "name": "Oxaliplatin", "type": "DRUG" }, { "name": "5-Fluorouracil", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 37, "start_date": "2016-11-03", "completion_date": "2023-03-14", "has_results": true, "last_update_posted_date": "2023-03-16", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 8, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Montvale, New Jersey + 5 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/NCT02954536" }, { "nct_id": "NCT05509998", "title": "Reducing the Duration of Untreated Psychosis in the United States: The Impact of Screening and Systematic Communication", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "First Episode Psychosis (FEP)", "Clinical High Risk for Psychosis (CHR)" ], "interventions": [ { "name": "Screening Method (SM)", "type": "BEHAVIORAL" }, { "name": "Screening and Communication Method (SCM)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Icahn School of Medicine at Mount Sinai", "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": 912, "start_date": "2023-05-01", "completion_date": "2027-04-30", "has_results": false, "last_update_posted_date": "2026-09-18", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05509998" }, { "nct_id": "NCT06041581", "title": "SHADES Mechanistic Trial", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Insomnia", "Insomnia Chronic", "Insomnia, Primary", "Sleep Disturbance", "Sleep Disorder", "Cardiovascular Diseases", "Heart Diseases", "Coronary Artery Disease", "Stroke", "Autonomic Dysfunction", "Systemic Inflammatory Response", "Metabolic Disease" ], "interventions": [ { "name": "Sleep Healthy Using The Internet (SHUTi)", "type": "BEHAVIORAL" }, { "name": "Telephonic CBT-I", "type": "BEHAVIORAL" }, { "name": "Face-to-Face CBT-I", "type": "BEHAVIORAL" }, { "name": "Active Control: Sleep Education/Hygiene, Symptom Monitoring, and Usual Primary Care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 200, "start_date": "2024-04-25", "completion_date": "2027-07-31", "has_results": false, "last_update_posted_date": "2026-08-06", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT06041581" }, { "nct_id": "NCT05473936", "title": "A CHW Intervention to Identify and Decrease Barriers to COVID 19 Testing & Vaccination", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vaccine Hesitancy", "COVID-19 Testing", "Community Health Workers" ], "interventions": [ { "name": "Community Health Worker led curriculum", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Charles Drew University of Medicine and Science", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "16 Years", "maximum_age": null, "sex": "ALL", "summary": "16 Years and older" }, "enrollment_count": 66, "start_date": "2022-10-11", "completion_date": "2023-05", "has_results": false, "last_update_posted_date": "2023-03-02", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 2, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05473936" }, { "nct_id": "NCT02735577", "title": "Neural Mechanisms of Disulfiram Effects", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Alcohol Use Disorder" ], "interventions": [ { "name": "Disulfiram", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "New York State Psychiatric Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "21 Years to 60 Years" }, "enrollment_count": 7, "start_date": "2016-03", "completion_date": "2020-10-16", "has_results": true, "last_update_posted_date": "2020-11-23", "last_synced_at": "2026-10-05T03:36:11.156Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02735577" } ] }