{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Best+Practices&page=22", "query": { "intervention": "Best Practices", "page": 22 }, "page_size": 10 }, "pagination": { "page": 22, "page_size": 10, "total_count": 741, "total_pages": 75, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Best+Practices&page=23&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Best+Practices&page=21&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-30T18:18:59.061Z", "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": "NCT03185741", "title": "Regimen Education and Messaging in Diabetes (REMinD)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus, Type 2", "Medication Adherence" ], "interventions": [ { "name": "UMS Strategy", "type": "BEHAVIORAL" }, { "name": "SMS Text Messaging", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 767, "start_date": "2018-01-05", "completion_date": "2022-11-30", "has_results": true, "last_update_posted_date": "2023-03-10", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 2, "location_summary": "Chicago, Illinois • New York, New York", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03185741" }, { "nct_id": "NCT04959474", "title": "Pre-operative SABR With and Without Caloric Restriction for Early Stage Breast Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anatomic Stage 0 Breast Cancer AJCC v8", "Anatomic Stage 1 Breast Cancer AJCC v8", "Anatomic Stage 2 Breast Cancer AJCC v8", "Anatomic Stage 3 Breast Cancer AJCC v8", "Breast Ductal Carcinoma in Situ", "Invasive Breast Carcinoma", "Triple Negative Breast Carcinoma" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Stereotactic Body Radiation Therapy", "type": "RADIATION" }, { "name": "Resection", "type": "PROCEDURE" }, { "name": "Sentinel Lymph Node Biopsy", "type": "PROCEDURE" }, { "name": "Dietary Intervention", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Mammography", "type": "PROCEDURE" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "RADIATION", "PROCEDURE" ], "sponsor": "Thomas Jefferson University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 80, "start_date": "2021-08-23", "completion_date": "2028-11-01", "has_results": false, "last_update_posted_date": "2026-01-23", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04959474" }, { "nct_id": "NCT06377696", "title": "Remote Cognitive Assessment and Wearable Device While Assessing the Impact of Metformin in Patients With History of Cranial Radiation Therapy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Malignant Brain Neoplasm" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Medical Device Usage and Evaluation", "type": "OTHER" }, { "name": "Metformin", "type": "DRUG" }, { "name": "Neurocognitive Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2024-05-31", "completion_date": "2028-02-01", "has_results": false, "last_update_posted_date": "2026-10-02", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06377696" }, { "nct_id": "NCT05021172", "title": "Incorporating ePrognosis for the Encouragement of Smarter Screening for Breast and Colorectal Cancer in Older Adults", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Carcinoma", "Colorectal Carcinoma" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Informational Intervention", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "70 Years", "maximum_age": null, "sex": "ALL", "summary": "70 Years and older" }, "enrollment_count": 75, "start_date": "2021-08-24", "completion_date": "2022-06-30", "has_results": false, "last_update_posted_date": "2022-07-11", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05021172" }, { "nct_id": "NCT01537874", "title": "MassCONECT (Massachusetts Community Networks to Eliminate Cancer Disparities Through Education) 4 Kids: Promoting Smoke-free Homes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tobacco Smoking Behavior" ], "interventions": [ { "name": "Motivational Interview", "type": "BEHAVIORAL" }, { "name": "Usual best practices", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Harvard School of Public Health (HSPH)", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "17 Years", "maximum_age": null, "sex": "ALL", "summary": "17 Years and older" }, "enrollment_count": 138, "start_date": "2010-05", "completion_date": "2013-04", "has_results": false, "last_update_posted_date": "2014-05-20", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 3, "location_summary": "Boston, Massachusetts • Lawrence, Massachusetts • Worcester, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Lawrence", "state": "Massachusetts" }, { "city": "Worcester", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01537874" }, { "nct_id": "NCT05874297", "title": "Online Nutrition Education to Decrease the Side Effects of Chemotherapy in Patients With Breast Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anatomic Stage I Breast Cancer AJCC v8", "Anatomic Stage II Breast Cancer AJCC v8", "Anatomic Stage III Breast Cancer AJCC v8" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Internet-Based Intervention", "type": "BEHAVIORAL" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Fred Hutchinson 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": 50, "start_date": "2026-07-15", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-08-06", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT05874297" }, { "nct_id": "NCT05132296", "title": "Mobile-Health Delivery of Lifestyle Interventions for Women With Breast Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Carcinoma" ], "interventions": [ { "name": "Behavioral Intervention", "type": "BEHAVIORAL" }, { "name": "Best Practice", "type": "OTHER" }, { "name": "FitBit", "type": "DEVICE" }, { "name": "Nutrition Education", "type": "BEHAVIORAL" }, { "name": "Physical Activity", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "DEVICE" ], "sponsor": "M.D. Anderson 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": 30, "start_date": "2021-05-21", "completion_date": "2026-06-15", "has_results": false, "last_update_posted_date": "2026-06-12", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 2, "location_summary": "Winston-Salem, North Carolina • Houston, Texas", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05132296" }, { "nct_id": "NCT07011420", "title": "Effects of Myoelectric Channel Count and Targeting for Upper Limb Prosthetic Control", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Amputation", "Amputation, Traumatic", "Amputation, Congenital", "Prosthesis User", "Upper Limb Amputation Below Elbow (Injury)", "Amputation; Traumatic, Arm: Forearm, Between Elbow and Wrist" ], "interventions": [ { "name": "Experimental socket with 4 untargeted channels active", "type": "DEVICE" }, { "name": "Experimental socket with 8 untargeted channels active", "type": "DEVICE" }, { "name": "Experimental socket with up to 16 untargeted channels active", "type": "DEVICE" }, { "name": "Experimental socket with 8 targeted channels active", "type": "DEVICE" }, { "name": "Coapt EMG Cuff", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Liberating Technologies, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 32, "start_date": "2025-10", "completion_date": "2026-06", "has_results": false, "last_update_posted_date": "2025-09-03", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 2, "location_summary": "Chicago, Illinois • Holliston, Massachusetts", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Holliston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07011420" }, { "nct_id": "NCT02157597", "title": "NIRS Guidance Trail in Children's Heart Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Heart Defects, Congenital" ], "interventions": [ { "name": "NIRS based management", "type": "OTHER" }, { "name": "Control", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Children's Hospital Medical Center, Cincinnati", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "1 Day", "maximum_age": "6 Months", "sex": "ALL", "summary": "1 Day to 6 Months" }, "enrollment_count": 73, "start_date": "2011-11", "completion_date": "2016-01", "has_results": false, "last_update_posted_date": "2016-05-12", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 1, "location_summary": "Cincinnati, Ohio", "locations": [ { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02157597" }, { "nct_id": "NCT04411849", "title": "Multilevel HPV Self-Testing Intervention for the Increase of Cervical Cancer Screening Among Women in Appalachia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cervical Carcinoma", "Human Papillomavirus Infection" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "HPV Self-Collection", "type": "PROCEDURE" }, { "name": "Informational Intervention", "type": "OTHER" }, { "name": "Patient Navigation Program", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "PROCEDURE", "BEHAVIORAL" ], "sponsor": "Ohio State University Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "64 Years", "sex": "FEMALE", "summary": "30 Years to 64 Years · Female only" }, "enrollment_count": 802, "start_date": "2021-08-27", "completion_date": "2024-06-11", "has_results": true, "last_update_posted_date": "2025-09-10", "last_synced_at": "2026-10-30T18:18:59.061Z", "location_count": 4, "location_summary": "Lexington, Kentucky • Columbus, Ohio • Charlottesville, Virginia + 1 more", "locations": [ { "city": "Lexington", "state": "Kentucky" }, { "city": "Columbus", "state": "Ohio" }, { "city": "Charlottesville", "state": "Virginia" }, { "city": "Morgantown", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04411849" } ] }