{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Counseling+and+active+drug+intervention&page=3", "query": { "intervention": "Counseling and active drug intervention", "page": 3 }, "page_size": 10 }, "pagination": { "page": 3, "page_size": 10, "total_count": 134, "total_pages": 14, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Counseling+and+active+drug+intervention&page=4&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Counseling+and+active+drug+intervention&page=2&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-12T11:15:47.447Z", "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": "NCT07789132", "title": "Evaluation of Community Health Worker Support to Help People With Serious Mental Illness to Quit Smoking", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Nicotine Dependance", "Serious Mental Illness", "Smoking (Tobacco) Addiction", "Tobacco Cessation", "Community Health Workers", "Cardiovascular (CV) Risk", "Tobacco Use Disorder" ], "interventions": [ { "name": "Integrated CHW Support intervention", "type": "BEHAVIORAL" }, { "name": "Enhanced usual care (EUC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 937, "start_date": "2026-10-01", "completion_date": "2030-10", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07789132" }, { "nct_id": "NCT01378780", "title": "Stroke Health and Risk Education (SHARE)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Hypertension" ], "interventions": [ { "name": "Educational intervention for diet and physical activity", "type": "BEHAVIORAL" }, { "name": "Educational message on skin cancer awareness", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 760, "start_date": "2011-05", "completion_date": "2013-12", "has_results": false, "last_update_posted_date": "2015-04-28", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "Corpus Christi, Texas", "locations": [ { "city": "Corpus Christi", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01378780" }, { "nct_id": "NCT06616363", "title": "Does a Periaqueductal Gray-vagus Nerve Interface Malfunction Explain the Nat hx With Its Numerous Co-morbidities?", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "POTS - Postural Orthostatic Tachycardia Syndrome" ], "interventions": [ { "name": "Questionnaires to be competed", "type": "BEHAVIORAL" }, { "name": "Provide list of medication and lifetime events", "type": "BEHAVIORAL" }, { "name": "Use phone App to record new life events", "type": "BEHAVIORAL" }, { "name": "Will wear an activity monitor", "type": "DEVICE" }, { "name": "Periodic 24-hour urine sodium check", "type": "OTHER" }, { "name": "A fMRI scan", "type": "DIAGNOSTIC_TEST" }, { "name": "A bedside tilt test will be performed", "type": "DIAGNOSTIC_TEST" }, { "name": "IV placed to collect blood samples", "type": "OTHER" }, { "name": "Stool Sample", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE", "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Virginia Commonwealth University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "21 Years", "sex": "FEMALE", "summary": "12 Years to 21 Years · Female only" }, "enrollment_count": 120, "start_date": "2024-05-29", "completion_date": "2028-07", "has_results": false, "last_update_posted_date": "2026-09-29", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06616363" }, { "nct_id": "NCT01726803", "title": "Comparative Effectiveness of Acute Low Back Pain Management", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Low Back Pain" ], "interventions": [ { "name": "Early Physical Therapy with Usual Care", "type": "OTHER" }, { "name": "Usual Care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 220, "start_date": "2011-04", "completion_date": "2014-11", "has_results": true, "last_update_posted_date": "2018-10-09", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 2, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" }, { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT01726803" }, { "nct_id": "NCT03125915", "title": "Addressing Substance Use Through CVCT", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sex, Unsafe", "Drug Use" ], "interventions": [ { "name": "Communication skills training video", "type": "BEHAVIORAL" }, { "name": "substance use module", "type": "BEHAVIORAL" }, { "name": "Couples HIV Testing and Counseling", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Hunter College of City University of New York", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "MALE", "summary": "18 Years to 60 Years · Male only" }, "enrollment_count": 140, "start_date": "2014-04-01", "completion_date": "2018-02-01", "has_results": true, "last_update_posted_date": "2021-04-15", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03125915" }, { "nct_id": "NCT07124728", "title": "Syntrillo Telehealth Stroke Risk Reduction Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension", "Hypertension (HTN)", "Stroke Prevention", "Cardiovascular Risk Factor" ], "interventions": [ { "name": "Technology-enabled Telehealth Care Plan", "type": "BEHAVIORAL" }, { "name": "Blood Pressure Monitoring Device", "type": "DEVICE" }, { "name": "Tenovi Smart Pillbox", "type": "DEVICE" }, { "name": "Wearable Activity Trackers (Fitbit or Apple Watch)", "type": "DEVICE" }, { "name": "Healthie EHR", "type": "OTHER" }, { "name": "Secure Messaging Platforms (TigerConnect, Weave, AirCall)", "type": "OTHER" }, { "name": "Antihypertensive Medication Management", "type": "DRUG" }, { "name": "Statin Medication Management", "type": "DRUG" }, { "name": "Antiplatelet or Anticoagulant Therapy", "type": "DRUG" }, { "name": "Laboratory Blood Test Collection", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE", "OTHER", "DRUG", "PROCEDURE" ], "sponsor": "Syntrillo, Inc", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": null, "sex": "ALL", "summary": "30 Years and older" }, "enrollment_count": 11, "start_date": "2025-07-30", "completion_date": "2026-07-22", "has_results": false, "last_update_posted_date": "2026-07-30", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07124728" }, { "nct_id": "NCT01120704", "title": "Evaluation of Treatments to Improve Smoking Cessation Medication Adherence", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Smoking", "Smoking Cessation", "Adherence", "Nicotine Dependence", "Motivation" ], "interventions": [ { "name": "Short Term Combination Nicotine Replacement Therapy (patch + gum)", "type": "DRUG" }, { "name": "Long Term Combination Nicotine Replacement Therapy (patch + gum)", "type": "DRUG" }, { "name": "Intensive Maintenance Counseling", "type": "BEHAVIORAL" }, { "name": "Cognitive Medication Adherence Counseling (CAM)", "type": "BEHAVIORAL" }, { "name": "Electronic Medication Monitoring Device (the Helping Hand) + Feedback", "type": "BEHAVIORAL" }, { "name": "Automated Adherence Prompting Phone Calls", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 544, "start_date": "2010-06", "completion_date": "2014-05", "has_results": true, "last_update_posted_date": "2015-12-11", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT01120704" }, { "nct_id": "NCT00974402", "title": "Psychotherapy Treatment of Deployment-Related PTSD in Primary Care Settings", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-Traumatic Stress Disorders", "Stress Disorders", "Combat Disorders" ], "interventions": [ { "name": "Cognitive Behavioral Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "The University of Texas Health Science Center at San Antonio", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 35, "start_date": "2008-03", "completion_date": "2012-06", "has_results": false, "last_update_posted_date": "2014-09-18", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 3, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" }, { "city": "San Antonio", "state": "Texas" }, { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00974402" }, { "nct_id": "NCT06212557", "title": "KIOS Mobile App Evaluation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid Use Disorder" ], "interventions": [ { "name": "KIOS App", "type": "DEVICE" }, { "name": "KIOS App education", "type": "BEHAVIORAL" }, { "name": "Treatment as usual", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "The University of Texas Health Science Center at San Antonio", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 116, "start_date": "2024-05-02", "completion_date": "2025-12-29", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06212557" }, { "nct_id": "NCT06534918", "title": "Precise Oncology Interventions in Nutrition and Training (OnPoint)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Prostate Cancer", "Colorectal Cancer", "Lymphoma" ], "interventions": [ { "name": "Fitbit", "type": "OTHER" }, { "name": "Nutrition Course: Group Sessions", "type": "BEHAVIORAL" }, { "name": "Physical Activity Program: Group Sessions", "type": "BEHAVIORAL" }, { "name": "Nutrition Course: One on One Sessions with Registered Dietitian", "type": "BEHAVIORAL" }, { "name": "Physical Activity Program: One on One Sessions with an Exercise Physiologist", "type": "BEHAVIORAL" }, { "name": "Nutrition and Physical Activity Prescription", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 306, "start_date": "2024-09-18", "completion_date": "2027-09-30", "has_results": false, "last_update_posted_date": "2026-09-23", "last_synced_at": "2026-10-12T11:15:47.447Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06534918" } ] }