{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Minimal+Contact", "query": { "intervention": "Minimal Contact" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 113, "total_pages": 12, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Minimal+Contact&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-06T21:44:06.661Z", "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": "NCT03512210", "title": "Monitoring SOF/VEL in Treatment Naïve, HCV Participants With Active Infection", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Hepatitis C", "HIV-1-infection", "Liver Diseases" ], "interventions": [ { "name": "Sofosbuvir/Velpatasvir (SOF/VEL)", "type": "DRUG" }, { "name": "Minimal Monitoring (MINMON) Strategy", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 400, "start_date": "2018-10-22", "completion_date": "2021-02-28", "has_results": true, "last_update_posted_date": "2022-02-04", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 30, "location_summary": "Birmingham, Alabama • Los Angeles, California • San Diego, California + 22 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03512210" }, { "nct_id": "NCT05307939", "title": "A Study on Using Cell-Free Tumor DNA (ctDNA) Testing to Decide When to StartRoutine Treatment in People With Human Papilloma Virus (HPV)- Associated Oropharynx Cancer (OPC)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "HPV", "Oropharynx Cancer", "HPV-Related Carcinoma", "HPV-Related Malignancy", "HPV Positive Oropharyngeal Squamous Cell Carcinoma" ], "interventions": [ { "name": "HPV ctDNA Assay", "type": "DIAGNOSTIC_TEST" }, { "name": "MRI Studies", "type": "DIAGNOSTIC_TEST" }, { "name": "EORTC QLQ H&N 35 and C30", "type": "BEHAVIORAL" }, { "name": "MDADI-HN", "type": "BEHAVIORAL" }, { "name": "COST-FACIT", "type": "BEHAVIORAL" }, { "name": "Intensity-Modulated Radiation Therapy (Arm A)", "type": "RADIATION" }, { "name": "Chemoradiation (Arm B)", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "BEHAVIORAL", "RADIATION", "COMBINATION_PRODUCT" ], "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": 30, "start_date": "2022-03-24", "completion_date": "2027-03-24", "has_results": false, "last_update_posted_date": "2026-04-13", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 8, "location_summary": "Miami, Florida • Basking Ridge, New Jersey • Middletown, New Jersey + 5 more", "locations": [ { "city": "Miami", "state": "Florida" }, { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05307939" }, { "nct_id": "NCT00876941", "title": "Assessing Screening Plus Brief Intervention's Resulting Efficacy (ASPIRE) to Stop Drug Use", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Drug Usage", "Drug Abuse", "Drug Dependence" ], "interventions": [ { "name": "Standard Brief Intervention", "type": "BEHAVIORAL" }, { "name": "Enhanced Brief Intervention", "type": "BEHAVIORAL" }, { "name": "Control: Information and Feedback", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Boston Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 589, "start_date": "2009-04", "completion_date": "2014-09", "has_results": false, "last_update_posted_date": "2014-10-02", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00876941" }, { "nct_id": "NCT03187119", "title": "Investigation of the Role of Pictorial Asthma Action Plans to Promote Self-management in Rural Youth With Asthma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Asthma" ], "interventions": [ { "name": "Pictorial Asthma Action Plan", "type": "BEHAVIORAL" }, { "name": "Written Asthma Action Plan", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "West Virginia University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "8 Years to 17 Years" }, "enrollment_count": 45, "start_date": "2017-05-24", "completion_date": "2018-11-12", "has_results": true, "last_update_posted_date": "2021-10-22", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 1, "location_summary": "Morgantown, West Virginia", "locations": [ { "city": "Morgantown", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03187119" }, { "nct_id": "NCT06444295", "title": "Testing the Impact of Thrive App Versions on Alcohol Use and Posttraumatic Stress After Recent Sexual Assault", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Posttraumatic Stress Symptom", "Alcohol Drinking", "Alcohol Problem" ], "interventions": [ { "name": "Activity scheduling", "type": "BEHAVIORAL" }, { "name": "Cognitive restructuring", "type": "BEHAVIORAL" }, { "name": "Coaching calls", "type": "BEHAVIORAL" }, { "name": "Non-core intervention components", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 464, "start_date": "2024-07-29", "completion_date": "2027-07-15", "has_results": false, "last_update_posted_date": "2026-08-10", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06444295" }, { "nct_id": "NCT05586542", "title": "Study to Assess the Safety of DERMASEAL for Diabetic Foot Ulcers", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Foot Ulcer, Diabetic" ], "interventions": [ { "name": "DERMASEAL", "type": "COMBINATION_PRODUCT" }, { "name": "Plasma Film", "type": "BIOLOGICAL" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "COMBINATION_PRODUCT", "BIOLOGICAL", "OTHER" ], "sponsor": "Vitruvian Medical Devices, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 26, "start_date": "2022-10-03", "completion_date": "2025-04-30", "has_results": false, "last_update_posted_date": "2024-12-27", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 4, "location_summary": "Fresno, California • South Miami, Florida • Boardman, Ohio + 1 more", "locations": [ { "city": "Fresno", "state": "California" }, { "city": "South Miami", "state": "Florida" }, { "city": "Boardman", "state": "Ohio" }, { "city": "McAllen", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05586542" }, { "nct_id": "NCT02494869", "title": "Dose-Response of Aerobic Training in Women at High-Risk for Development of Breast Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "High Risk for Developing Breast Cancer" ], "interventions": [ { "name": "Nonlinear Aerobic Training", "type": "BEHAVIORAL" }, { "name": "Height, Weight, BMI measure", "type": "OTHER" }, { "name": "Blood draw", "type": "OTHER" }, { "name": "Cardiopulmonary exercise test", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 75, "start_date": "2015-07", "completion_date": "2027-07", "has_results": false, "last_update_posted_date": "2026-08-05", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02494869" }, { "nct_id": "NCT04124341", "title": "PCS in Severe Treatment Resistant Depression", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Treatment Resistant Depression" ], "interventions": [ { "name": "Prefrontal Cortical Stimulation (PCS)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "22 Years to 70 Years" }, "enrollment_count": 15, "start_date": "2021-09-29", "completion_date": "2032-12-31", "has_results": false, "last_update_posted_date": "2026-09-01", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT04124341" }, { "nct_id": "NCT05441709", "title": "Furthering Equity Through Infant Feeding EDucation and Support", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breastfeeding" ], "interventions": [ { "name": "Ci-BPC with Standard of Care (SOC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Endeavor Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 990, "start_date": "2022-11-08", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2025-12-09", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 4, "location_summary": "Chicago, Illinois • Evanston, Illinois • Highland Park, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Evanston", "state": "Illinois" }, { "city": "Highland Park", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05441709" }, { "nct_id": "NCT03380026", "title": "Mechlorethamine Induced Contact Dermatitis Avoidance Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Cutaneous T-cell Lymphoma", "Cutaneous T-cell Lymphoma Stage I", "Mycosis Fungoides", "Folliculotropic Mycosis Fungoides", "Granulomatous Slack Skin", "Syringotropic Mycosis Fungoides", "Mycosis Fungoides Variant", "Transformed Mycosis Fungoides" ], "interventions": [ { "name": "Triamcinolone", "type": "DRUG" }, { "name": "Valchlor 0.016 % Topical Gel", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Rochester Skin Lymphoma Medical Group, PLLC", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 28, "start_date": "2017-12-13", "completion_date": "2020-12-13", "has_results": true, "last_update_posted_date": "2026-09-04", "last_synced_at": "2026-09-06T21:44:06.661Z", "location_count": 1, "location_summary": "Fairport, New York", "locations": [ { "city": "Fairport", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03380026" } ] }