{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Track+B&page=2", "query": { "intervention": "Track B", "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=Track+B&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-11T20:11:10.366Z", "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": "NCT04769986", "title": "Mobile Mindfulness for Alcohol Use and PTSD Among Veterans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alcohol Use Disorder", "Posttraumatic Stress Disorder" ], "interventions": [ { "name": "Mobile Mindfulness-Relapse Prevention (mMBRP)", "type": "BEHAVIORAL" }, { "name": "Exercise/healthy eating mobile app", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Southern California", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 201, "start_date": "2021-01-01", "completion_date": "2024-08-31", "has_results": false, "last_update_posted_date": "2024-11-15", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 3, "location_summary": "Los Angeles, California • Menlo Park, California • San Francisco, California", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Menlo Park", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04769986" }, { "nct_id": "NCT05783635", "title": "Alcohol Screening and Preoperative Intervention Research Study - 2", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alcohol Drinking" ], "interventions": [ { "name": "Enhanced Usual Care (pre-operative)", "type": "BEHAVIORAL" }, { "name": "Preoperative Virtual Health Coaching", "type": "BEHAVIORAL" }, { "name": "Usual surgical care (post-operative)", "type": "BEHAVIORAL" }, { "name": "Postoperative Virtual Health Coaching", "type": "BEHAVIORAL" }, { "name": "On-Track (Post-operative)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "21 Years to 75 Years" }, "enrollment_count": 440, "start_date": "2023-04-17", "completion_date": "2027-02-28", "has_results": false, "last_update_posted_date": "2026-08-10", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05783635" }, { "nct_id": "NCT07040280", "title": "Testing the Effect of Sulforaphane, a Compound Naturally Found in Cruciferous Vegetables, on Preventing Melanoma in Patients With a Prior History of Melanoma", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Melanoma" ], "interventions": [ { "name": "Sulforaphane (broccoli sprout extract)", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Derma-AI", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "Eastern Cooperative Oncology Group", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2025-10-31", "completion_date": "2029-08-01", "has_results": false, "last_update_posted_date": "2025-06-27", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07040280" }, { "nct_id": "NCT04562233", "title": "Breast Cancer and Resistance Exercise Program", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Resistance Training" ], "interventions": [ { "name": "Online-delivered physical activity intervention.", "type": "BEHAVIORAL" }, { "name": "Printed, individualized resistance-based physical activity program.", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rutgers, The State University of New Jersey", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 56, "start_date": "2020-12-01", "completion_date": "2023-08-24", "has_results": false, "last_update_posted_date": "2023-10-13", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "New Brunswick, New Jersey", "locations": [ { "city": "New Brunswick", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT04562233" }, { "nct_id": "NCT07374315", "title": "Weight Gain in Pediatric Leukemia Survivors", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Leukemia", "Pediatric Acute Lymphoblastic Leukemia", "Pediatric Acute Lymphoblastic Leukemia in Remission", "Pediatric Obesity" ], "interventions": [ { "name": "Modified Guided Self-Help Family Intervention", "type": "BEHAVIORAL" }, { "name": "NIH Educational Resources", "type": "BEHAVIORAL" }, { "name": "FitBit Ace", "type": "BEHAVIORAL" }, { "name": "WashU Extended Learning Canvas", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "6 Years", "maximum_age": null, "sex": "ALL", "summary": "6 Years and older" }, "enrollment_count": 80, "start_date": "2026-08-31", "completion_date": "2029-05-31", "has_results": false, "last_update_posted_date": "2026-07-24", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT07374315" }, { "nct_id": "NCT03689179", "title": "Virtual Coaching to Maximize Dementia Caregivers' Respite Time Use", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anxiety", "Burden, Dependency", "Caregiver" ], "interventions": [ { "name": "Time for Living and Caring (TLC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 166, "start_date": "2020-10-20", "completion_date": "2024-05-01", "has_results": true, "last_update_posted_date": "2024-10-15", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT03689179" }, { "nct_id": "NCT02148523", "title": "Social Forces to Improve Statin Adherence (Study B)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Medication Adherence", "High Blood Pressure", "Diabetes" ], "interventions": [ { "name": "Comparison to peers", "type": "BEHAVIORAL" }, { "name": "Adherence feedback", "type": "BEHAVIORAL" }, { "name": "Electronic pill bottle", "type": "DEVICE" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 201, "start_date": "2014-01", "completion_date": "2015-01", "has_results": true, "last_update_posted_date": "2017-07-13", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02148523" }, { "nct_id": "NCT06763549", "title": "COR-INSIGHT: Optimizing Cardiovascular and Cardiopulmonary Outcomes with AI-Driven Multiplexed Indications Using COR ECG Wearable", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cardiopulmonary Failure", "Myocardial Infarction (MI)", "Heart Decompensation", "Heart Failure", "HFrEF - Heart Failure with Reduced Ejection Fraction", "HFpEF - Heart Failure with Preserved Ejection Fraction", "Syncopation", "Syncope", "Ischemic Cardiovascular Disease", "STEMI", "STEMI (ST Elevation MI)", "Atrial Fibrillation (AF)", "Atrial Enlargement", "LVF", "Conduction Defect", "Conduction Abnormalities", "Heart Block", "Valvular Diseases", "Cardiac Output, Low", "Stroke Volume", "Stroke Volume Variation", "Hyperkalemia", "Hypercalcemia", "Hypocalcemia", "LV Dysfunction", "QT Prolongation", "Sudden Cardiac Death Due to Cardiac Arrhythmia", "Ventricular Arrhythmia", "Pacing", "Pacing Induced Dyssynchrony", "Silent Ischemia", "Pericarditis", "Sleep Related Breathing Disorder", "RSA", "Apnea, Obstructive", "Cardiac Output Measurement", "Respiratory Impedance", "CRT And/or ICD", "Infarction", "Cardiomyopathies, Primary", "Hypertrophy" ], "interventions": [ { "name": "SUBPROTOCOL A", "type": "DEVICE" }, { "name": "SUBPROTOCOL B", "type": "DEVICE" }, { "name": "SUBPROTOCOL C", "type": "DEVICE" }, { "name": "SUBPROTOCOL D", "type": "DEVICE" }, { "name": "SUBPROTOCOL E", "type": "DEVICE" }, { "name": "SUBPROTOCOL F", "type": "DEVICE" }, { "name": "SUBPROTOCOL G", "type": "DEVICE" }, { "name": "SUBPROTOCOL H", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Peerbridge Health, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15000, "start_date": "2024-11-16", "completion_date": "2026-04-15", "has_results": false, "last_update_posted_date": "2025-01-08", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "Melbourne, Florida", "locations": [ { "city": "Melbourne", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06763549" }, { "nct_id": "NCT03001024", "title": "WayToServe Español: Online Responsible Beverage Service Training for Spanish-Speaking Servers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alcoholic Intoxication" ], "interventions": [ { "name": "Implementation of WayToServe Español", "type": "BEHAVIORAL" }, { "name": "Usual and Customary RBS Training", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Klein Buendel, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 79, "start_date": "2016-12", "completion_date": "2021-10-31", "has_results": false, "last_update_posted_date": "2022-03-11", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 2, "location_summary": "Golden, Colorado • El Paso, Texas", "locations": [ { "city": "Golden", "state": "Colorado" }, { "city": "El Paso", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03001024" }, { "nct_id": "NCT04303676", "title": "Facilitating Alcohol Screening and Treatment (FAST)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alcohol Use Disorder" ], "interventions": [ { "name": "Virtual Practice Facilitation with e-Learning", "type": "OTHER" }, { "name": "Virtual Practice Facilitation without e-Learning", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 399, "start_date": "2020-05-26", "completion_date": "2023-04-13", "has_results": false, "last_update_posted_date": "2023-12-18", "last_synced_at": "2026-09-11T20:11:10.366Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04303676" } ] }