{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Supportive+therapy&page=48", "query": { "intervention": "Supportive therapy", "page": 48 }, "page_size": 10 }, "pagination": { "page": 48, "page_size": 10, "total_count": 5081, "total_pages": 509, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Supportive+therapy&page=49&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Supportive+therapy&page=47&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-25T16:12:50.485Z", "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": "NCT01049568", "title": "Cell Phone Reminders Intervention", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HAART Non-Adherence", "HIV", "HIV Infections" ], "interventions": [ { "name": "Cell Phone Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "15 Years", "maximum_age": "24 Years", "sex": "ALL", "summary": "15 Years to 24 Years" }, "enrollment_count": 43, "start_date": "2009-10", "completion_date": "2010-11", "has_results": false, "last_update_posted_date": "2017-02-28", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 5, "location_summary": "Los Angeles, California • San Francisco, California • Washington D.C., District of Columbia + 2 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Fort Lauderdale", "state": "Florida" }, { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT01049568" }, { "nct_id": "NCT06548074", "title": "H-PACE Program for the Improvement of Lifestyle Behaviors Among Children", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pediatric Obesity" ], "interventions": [ { "name": "H-PACE Behavioral Intervention", "type": "BEHAVIORAL" }, { "name": "Accelerometer", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Supportive Care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Fred Hutchinson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "8 Years", "maximum_age": null, "sex": "ALL", "summary": "8 Years and older" }, "enrollment_count": 122, "start_date": "2024-01-22", "completion_date": "2025-05-30", "has_results": true, "last_update_posted_date": "2026-07-14", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 2, "location_summary": "Las Cruces, New Mexico • Seattle, Washington", "locations": [ { "city": "Las Cruces", "state": "New Mexico" }, { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06548074" }, { "nct_id": "NCT02420990", "title": "Integrated Treatment for Adolescents With ADHD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "ADHD", "Substance Use Disorders" ], "interventions": [ { "name": "Medication Integration Protocol (MIP)", "type": "BEHAVIORAL" }, { "name": "Changing Academic Support in the Home for Adolescents with ADHD (CASH-AA)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "The National Center on Addiction and Substance Abuse at Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "12 Years to 18 Years" }, "enrollment_count": 145, "start_date": "2015-03-01", "completion_date": "2018-08-31", "has_results": true, "last_update_posted_date": "2022-10-14", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02420990" }, { "nct_id": "NCT06099197", "title": "I-CARE 2: Mobile Telehealth to Reduce Alzheimer'S-related Symptoms in Hispanic Individuals", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Caregiver Burden", "Alzheimer Disease" ], "interventions": [ { "name": "Brain CareNotes", "type": "BEHAVIORAL" }, { "name": "Dementia Guide Expert", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 16, "start_date": "2023-09-26", "completion_date": "2026-11", "has_results": false, "last_update_posted_date": "2026-08-17", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 1, "location_summary": "Bloomington, Indiana", "locations": [ { "city": "Bloomington", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT06099197" }, { "nct_id": "NCT02858310", "title": "E7 TCR T Cells for Human Papillomavirus-Associated Cancers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Papillomavirus Infections", "Cervical Intraepithelial Neoplasia", "Carcinoma In Situ", "Vulvar Neoplasms", "Vulvar Diseases" ], "interventions": [ { "name": "E7 TCR cells", "type": "BIOLOGICAL" }, { "name": "Aldesleukin", "type": "DRUG" }, { "name": "Fludarabine", "type": "DRUG" }, { "name": "Cyclophosphamide", "type": "DRUG" }, { "name": "EKG", "type": "DIAGNOSTIC_TEST" }, { "name": "Biopsy", "type": "PROCEDURE" }, { "name": "Chest CT and MRI or PET", "type": "DIAGNOSTIC_TEST" }, { "name": "PFT", "type": "DIAGNOSTIC_TEST" }, { "name": "Granisetron", "type": "DRUG" }, { "name": "Ondansetron", "type": "DRUG" }, { "name": "Droperidol", "type": "DRUG" }, { "name": "Prochlorperazine", "type": "DRUG" }, { "name": "Diphenoxylate HCL", "type": "DRUG" }, { "name": "Atropine sulfate", "type": "DRUG" }, { "name": "Codeine sulfate", "type": "DRUG" }, { "name": "Loperamide", "type": "DRUG" }, { "name": "Indomethacin", "type": "DRUG" }, { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Diphenhydramine HCL", "type": "DRUG" }, { "name": "Hydroxyzine HCL", "type": "DRUG" }, { "name": "Meperidine", "type": "DRUG" } ], "intervention_types": [ "BIOLOGICAL", "DRUG", "DIAGNOSTIC_TEST", "PROCEDURE" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 224, "start_date": "2017-01-27", "completion_date": "2025-07-02", "has_results": true, "last_update_posted_date": "2026-03-09", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 2, "location_summary": "Bethesda, Maryland • New Brunswick, New Jersey", "locations": [ { "city": "Bethesda", "state": "Maryland" }, { "city": "New Brunswick", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT02858310" }, { "nct_id": "NCT00609882", "title": "Comparison of Humidified High Flow Nasal Cannula to Nasal CPAP in Neonates", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Respiratory Insufficiency" ], "interventions": [ { "name": "Nasal CPAP", "type": "OTHER" }, { "name": "Humidified High Flow Nasal Cannula (HHFNC)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "8 Weeks", "sex": "ALL", "summary": "Up to 8 Weeks" }, "enrollment_count": 420, "start_date": "2007-12", "completion_date": "2012-06", "has_results": false, "last_update_posted_date": "2013-02-06", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 8, "location_summary": "Philadelphia, Pennsylvania • Lackland Air Force Base, Texas • Ogden, Utah + 3 more", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Lackland Air Force Base", "state": "Texas" }, { "city": "Ogden", "state": "Utah" }, { "city": "Provo", "state": "Utah" }, { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT00609882" }, { "nct_id": "NCT01048749", "title": "Interventional Study of Effects on Spine Height With Two Unloading Positions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Low Back Pain" ], "interventions": [ { "name": "aquatic vertical suspension.", "type": "OTHER" }, { "name": "land-based supine flexion", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Texas Tech University Health Sciences Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "40 Years to 80 Years" }, "enrollment_count": 60, "start_date": "2008-08", "completion_date": "2009-06", "has_results": false, "last_update_posted_date": "2010-01-14", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 1, "location_summary": "Cleburne, Texas", "locations": [ { "city": "Cleburne", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01048749" }, { "nct_id": "NCT04887558", "title": "Mobile App for Smoking Cessation and Mental Health", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Smoking Cessation", "Mental Illness" ], "interventions": [ { "name": "Smart-T Mental Health+ and NRT", "type": "COMBINATION_PRODUCT" }, { "name": "QuitGuide + NRT", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "University of Oklahoma", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 64, "start_date": "2021-12-14", "completion_date": "2028-12", "has_results": false, "last_update_posted_date": "2026-05-01", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 1, "location_summary": "Oklahoma City, Oklahoma", "locations": [ { "city": "Oklahoma City", "state": "Oklahoma" } ], "official_url": "https://clinicaltrials.gov/study/NCT04887558" }, { "nct_id": "NCT00217035", "title": "Glutamine Enriched Total Parenteral Feeding and Proline Metabolism in Severely Burned Patients", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Burns" ], "interventions": [ { "name": "TPN or TPN enriched with glutamine", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "1997-08", "completion_date": "2010-01", "has_results": false, "last_update_posted_date": "2017-01-13", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00217035" }, { "nct_id": "NCT05826925", "title": "Optimizing Cardiovascular Preventive Care for Women Following Hypertensive Disorders of Pregnancy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension, Pregnancy Induced", "Hypertension Complicating Pregnancy", "Preeclampsia", "Cardiovascular Diseases", "Patient Engagement" ], "interventions": [ { "name": "Decision aid", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Utah", "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": 30, "start_date": "2026-07-15", "completion_date": "2027-08", "has_results": false, "last_update_posted_date": "2026-06-23", "last_synced_at": "2026-10-25T16:12:50.485Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT05826925" } ] }