{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Service+learning&page=26", "query": { "intervention": "Service learning", "page": 26 }, "page_size": 10 }, "pagination": { "page": 26, "page_size": 10, "total_count": 1890, "total_pages": 189, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Service+learning&page=27&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Service+learning&page=25&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-24T12:54:07.803Z", "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": "NCT05978128", "title": "Utilizing Advocates and Supporters to Increase Lung Cancer Screening Rates in Eligible Participants", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Carcinoma", "Lung Carcinoma" ], "interventions": [ { "name": "Health Education", "type": "BEHAVIORAL" }, { "name": "Health Promotion and Education", "type": "OTHER" }, { "name": "Patient Navigation", "type": "BEHAVIORAL" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Jonsson Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "40 Years to 80 Years" }, "enrollment_count": 800, "start_date": "2023-07-28", "completion_date": "2029-09-30", "has_results": false, "last_update_posted_date": "2025-11-10", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05978128" }, { "nct_id": "NCT00249756", "title": "Re-Entry MTC for Offenders With MICA Disorders", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mental Disorders", "Substance-Related Disorders" ], "interventions": [ { "name": "Re-entry Modified Therapeutic Community (Re-entry MTC)", "type": "BEHAVIORAL" }, { "name": "Parole Supervision and Case Management", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "National Development and Research Institutes, Inc.", "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": 610, "start_date": "2005-08", "completion_date": "2010-04", "has_results": false, "last_update_posted_date": "2013-09-02", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 3, "location_summary": "Caqon City, Colorado • Pueblo, Colorado • Sterling, Colorado", "locations": [ { "city": "Caqon City", "state": "Colorado" }, { "city": "Pueblo", "state": "Colorado" }, { "city": "Sterling", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT00249756" }, { "nct_id": "NCT00723853", "title": "REACH-OUT: Chicago Children's Diabetes Prevention Program", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity", "Type 2 Diabetes" ], "interventions": [ { "name": "Reach-Out Program, nutritional and exercise program", "type": "BEHAVIORAL" }, { "name": "Reach-In Program, standard of care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "9 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "9 Years to 65 Years" }, "enrollment_count": 131, "start_date": "2008-04", "completion_date": "2012-04", "has_results": false, "last_update_posted_date": "2013-09-05", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00723853" }, { "nct_id": "NCT04845230", "title": "Fresh RX: NHS 2020", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Premature Birth", "Birth Weight", "Post Partum Depression", "Health Care Utilization", "Nutrition Deficiency Due to Insufficient Food", "Housing Problems", "Fetal Complications", "Food Deprivation" ], "interventions": [ { "name": "FreshRx Nourishing Healthy Starts", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": "55 Years", "sex": "FEMALE", "summary": "14 Years to 55 Years · Female only" }, "enrollment_count": 750, "start_date": "2021-08-09", "completion_date": "2026-09-15", "has_results": false, "last_update_posted_date": "2022-11-29", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04845230" }, { "nct_id": "NCT00319436", "title": "Stage I Randomized Trial of Mentalization-Based Therapy for Substance Using Mothers of Infants and Toddlers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Maternal Substance Use", "Child Abuse and Neglect" ], "interventions": [ { "name": "Mentalizing Therapy for Substance Using Mothers", "type": "BEHAVIORAL" }, { "name": "Standard Parent Education for Substance Using Mothers", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 47, "start_date": "2004-08", "completion_date": "2009-03", "has_results": true, "last_update_posted_date": "2020-04-09", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT00319436" }, { "nct_id": "NCT06184737", "title": "iSIPsmarter: A Pilot RCT to Evaluate a Web-based Behavioral Intervention to Reduce Sugary Beverages Among Black Adults", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diet Habit", "Sugar-Sweetened Beverages" ], "interventions": [ { "name": "iSIPsmarter", "type": "BEHAVIORAL" }, { "name": "Patient Education (PE)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Virginia", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "110 Years", "sex": "ALL", "summary": "18 Years to 110 Years" }, "enrollment_count": 24, "start_date": "2024-01-12", "completion_date": "2026-03-17", "has_results": false, "last_update_posted_date": "2025-05-29", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06184737" }, { "nct_id": "NCT06822530", "title": "A Multilevel Intervention to Increase Colorectal Cancer Screening Tests in Patients With Abnormal Fecal Immunochemical Test Results, PROACT Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colorectal Carcinoma" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Educational Intervention", "type": "OTHER" }, { "name": "Electronic Health Record Review", "type": "OTHER" }, { "name": "Interview", "type": "OTHER" }, { "name": "Supportive Care", "type": "OTHER" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Fred Hutchinson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "45 Years to 75 Years" }, "enrollment_count": 682, "start_date": "2025-12-16", "completion_date": "2030-01-31", "has_results": false, "last_update_posted_date": "2026-06-22", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06822530" }, { "nct_id": "NCT01941784", "title": "Health Education Intervention in Reducing Weight Gain in Patients With Newly Diagnosed Stage I-IV Breast Cancer Undergoing Chemotherapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stage IA Breast Cancer", "Stage IB Breast Cancer", "Stage II Breast Cancer", "Stage IIIA Breast Cancer", "Stage IIIB Breast Cancer", "Stage IIIC Breast Cancer", "Stage IV Breast Cancer" ], "interventions": [ { "name": "educational intervention", "type": "OTHER" }, { "name": "counseling intervention", "type": "OTHER" }, { "name": "telephone-based intervention", "type": "BEHAVIORAL" }, { "name": "questionnaire administration", "type": "OTHER" }, { "name": "quality-of-life assessment", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "BEHAVIORAL", "PROCEDURE" ], "sponsor": "Wake Forest University Health Sciences", "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": 28, "start_date": "2013-11-25", "completion_date": "2017-04-12", "has_results": false, "last_update_posted_date": "2019-01-25", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01941784" }, { "nct_id": "NCT00441311", "title": "Dissemination of Colorectal Cancer Screening to Primary Care Physicians", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Colorectal Cancer" ], "interventions": [ { "name": "Academic Detailing", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "50 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "50 Years to 80 Years" }, "enrollment_count": 264, "start_date": "2003-05", "completion_date": "2006-09", "has_results": false, "last_update_posted_date": "2011-02-01", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00441311" }, { "nct_id": "NCT07810400", "title": "A Study Of Remote Patient Monitoring (RPM) Program For Cancer Patients Initiating Cancer-directed Therapy", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Lymphoma" ], "interventions": [ { "name": "Smart Phone Application-based Intervention - SHIELD", "type": "BEHAVIORAL" }, { "name": "AION TempShield", "type": "OTHER" }, { "name": "Questionnaires", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": null, "sex": "ALL", "summary": "1 Year and older" }, "enrollment_count": 470, "start_date": "2026-11-15", "completion_date": "2031-06-30", "has_results": false, "last_update_posted_date": "2026-09-11", "last_synced_at": "2026-10-24T12:54:07.803Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT07810400" } ] }