{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+Supervision&page=57", "query": { "intervention": "Standard Supervision", "page": 57 }, "page_size": 10 }, "pagination": { "page": 57, "page_size": 10, "total_count": 2962, "total_pages": 297, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+Supervision&page=58&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+Supervision&page=56&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-29T12:51:18.940Z", "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": "NCT05380440", "title": "Preventing Parental Opioid and/or Methamphetamine Addiction Within DHS-Involved Families: PRE-FAIR", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid-Related Disorders", "Stimulant-Related Disorder", "Child Neglect", "Mental Health Impairment" ], "interventions": [ { "name": "Prevention Adaptation of Families Actively Improving Relationships (PRE-FAIR)", "type": "BEHAVIORAL" }, { "name": "Standard Case Management and Referral", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Chestnut Health Systems", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "16 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "16 Years to 30 Years" }, "enrollment_count": 241, "start_date": "2021-06-09", "completion_date": "2025-08-31", "has_results": false, "last_update_posted_date": "2026-06-05", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "Eugene, Oregon", "locations": [ { "city": "Eugene", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT05380440" }, { "nct_id": "NCT03543189", "title": "Combination of Nivolumab Immunotherapy With Radiation Therapy and Androgen Deprivation Therapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Prostate Cancer", "Prostate Disease" ], "interventions": [ { "name": "Nivolumab", "type": "DRUG" }, { "name": "Brachytherapy", "type": "RADIATION" }, { "name": "External Beam Radiation Therapy", "type": "RADIATION" }, { "name": "Androgen Deprivation Therapy", "type": "DRUG" } ], "intervention_types": [ "DRUG", "RADIATION" ], "sponsor": "H. Lee Moffitt Cancer Center and Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 44, "start_date": "2018-10-03", "completion_date": "2026-06-19", "has_results": false, "last_update_posted_date": "2026-09-16", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03543189" }, { "nct_id": "NCT07218016", "title": "Accelerometer Measured Early Recovery After Prolapse Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pelvic Organ Prolapse", "Pelvic Organ Prolapse (POP)", "Pelvic Organ Prolapse Vaginal Surgery", "Pelvic Organ Prolapse, Patient Education" ], "interventions": [ { "name": "Postoperative Exercise regimen", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "NICHD Pelvic Floor Disorders Network", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "FEMALE", "summary": "18 Years to 99 Years · Female only" }, "enrollment_count": 288, "start_date": "2025-10-02", "completion_date": "2028-03-31", "has_results": false, "last_update_posted_date": "2026-04-27", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 7, "location_summary": "San Diego, California • Chicago, Illinois • Durham, North Carolina + 3 more", "locations": [ { "city": "San Diego", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Durham", "state": "North Carolina" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07218016" }, { "nct_id": "NCT04400409", "title": "Implementation of Vascular Care Team to Improve Medical Management of PAD Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Peripheral Artery Disease" ], "interventions": [ { "name": "Intervention A - Vascular Care + site 6MWT administration", "type": "OTHER" }, { "name": "Intervention B - Standard Care + site 6MWT administration", "type": "OTHER" }, { "name": "Intervention A - Vascular Care + CPC EQuIP 6MWT administration", "type": "OTHER" }, { "name": "Intervention B - Standard Care + CPC EQuIP 6MWT administration", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Colorado Prevention Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 166, "start_date": "2020-07-07", "completion_date": "2023-05-11", "has_results": false, "last_update_posted_date": "2024-02-08", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04400409" }, { "nct_id": "NCT03466398", "title": "Effects of a Remote Patient Monitoring Protocol on Glycemic Control in Adolescents With Type 1 Diabetes", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus", "Type 1 Diabetes Mellitus" ], "interventions": [ { "name": "Vivify Health RPM Protocol", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Texas Southwestern Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "13 Years to 18 Years" }, "enrollment_count": 0, "start_date": "2018-04-11", "completion_date": "2020-03-05", "has_results": false, "last_update_posted_date": "2020-05-14", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03466398" }, { "nct_id": "NCT03081416", "title": "\"THINK Trial: Treatment of Headache With IntraNasal Ketamine: A Randomized Controlled Trial Evaluating the Efficacy of Intranasal Ketamine Versus Standard Therapy in the Management of Primary Headache Syndromes in the Emergency Department\"", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Headache", "Intranasal Ketamine" ], "interventions": [ { "name": "Ketamine", "type": "DRUG" }, { "name": "Normal saline", "type": "DRUG" }, { "name": "Metoclopramide", "type": "DRUG" }, { "name": "Ketorolac", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Benadryl", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Brooke Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 80, "start_date": "2016-05", "completion_date": "2017-10", "has_results": false, "last_update_posted_date": "2018-01-18", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03081416" }, { "nct_id": "NCT05461014", "title": "RxWell in Pediatric IBD for Disease Management and Transition Readiness", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mental Health Issue", "Inflammatory Bowel Diseases" ], "interventions": [ { "name": "dCBI", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "16 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "16 Years to 25 Years" }, "enrollment_count": 7, "start_date": "2022-07-30", "completion_date": "2023-03-08", "has_results": false, "last_update_posted_date": "2023-06-12", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05461014" }, { "nct_id": "NCT01323348", "title": "Effect of Diabetes Education During Retinal Ophthalmology Visits on Diabetes Control", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Diabetes", "Diabetic Retinopathy" ], "interventions": [ { "name": "Diabetes Education", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Jaeb Center for Health Research", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1875, "start_date": "2011-10", "completion_date": "2015-01", "has_results": false, "last_update_posted_date": "2016-08-26", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 34, "location_summary": "Loma Linda, California • Santa Barbara, California • Fort Lauderdale, Florida + 29 more", "locations": [ { "city": "Loma Linda", "state": "California" }, { "city": "Santa Barbara", "state": "California" }, { "city": "Fort Lauderdale", "state": "Florida" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Lakeland", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01323348" }, { "nct_id": "NCT02677389", "title": "Survivorship Care Plan in Promoting Physical Activity in Breast or Colorectal Cancer Survivors in Wisconsin", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer Survivor", "Healthy Subject", "Stage I Colorectal Cancer", "Stage IA Breast Cancer", "Stage IB Breast Cancer", "Stage IIA Breast Cancer", "Stage IIA Colorectal Cancer", "Stage IIB Breast Cancer", "Stage IIB Colorectal Cancer", "Stage IIC Colorectal Cancer", "Stage IIIA Breast Cancer", "Stage IIIA Colorectal Cancer", "Stage IIIB Breast Cancer", "Stage IIIB Colorectal Cancer", "Stage IIIC Breast Cancer", "Stage IIIC Colorectal Cancer" ], "interventions": [ { "name": "Educational Intervention", "type": "OTHER" }, { "name": "Internet-Based Intervention", "type": "OTHER" }, { "name": "Monitoring Device", "type": "DEVICE" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "30 Years to 75 Years" }, "enrollment_count": 100, "start_date": "2016-07-01", "completion_date": "2018-01-24", "has_results": false, "last_update_posted_date": "2019-11-18", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT02677389" }, { "nct_id": "NCT00683280", "title": "Contingency Management and Pharmacotherapy for Smoking Cessation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cigarette Smoking" ], "interventions": [ { "name": "contingency management", "type": "BEHAVIORAL" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "UConn Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 59, "start_date": "2008-05", "completion_date": "2010-08", "has_results": false, "last_update_posted_date": "2018-01-16", "last_synced_at": "2026-10-29T12:51:18.940Z", "location_count": 1, "location_summary": "Farmington, Connecticut", "locations": [ { "city": "Farmington", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT00683280" } ] }