{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Small+portion&page=5", "query": { "intervention": "Small portion", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 1860, "total_pages": 186, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Small+portion&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Small+portion&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-20T03:04:19.223Z", "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": "NCT05761964", "title": "Harmony & Health: Feasibility of a Movement Intervention to Improve Psychosocial Wellbeing in Black Adults in Northeast Texas", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Psychological" ], "interventions": [ { "name": "Harmony & Health", "type": "BEHAVIORAL" }, { "name": "Health Education", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "M.D. Anderson 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": 50, "start_date": "2023-12-18", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-07-16", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05761964" }, { "nct_id": "NCT06351787", "title": "Project Soma: Cortical Activity of a Body Scan Meditation and Yoga Practice in Healthy Yogis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Well-Being, Psychological" ], "interventions": [ { "name": "Resting and movement-based focused awareness meditations", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Ohio University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 14, "start_date": "2022-10-31", "completion_date": "2023-06-28", "has_results": false, "last_update_posted_date": "2024-04-08", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "Athens, Ohio", "locations": [ { "city": "Athens", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT06351787" }, { "nct_id": "NCT02394587", "title": "MBSR for Pain Catastrophizing in SCD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anemia, Sickle Cell" ], "interventions": [ { "name": "Mindfulness-based Stress Reduction", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2015-04", "completion_date": "2016-01", "has_results": false, "last_update_posted_date": "2017-12-29", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02394587" }, { "nct_id": "NCT07864714", "title": "UltraTrac Clinical Pilot Study", "overall_status": "NOT_YET_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Hemodynamic Monitoring" ], "interventions": [ { "name": "Noninvasive Hemodynamic Monitoring System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "AcQumen Medical, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "0 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "0 Years to 21 Years" }, "enrollment_count": 50, "start_date": "2026-10", "completion_date": "2027-10", "has_results": false, "last_update_posted_date": "2026-10-08", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07864714" }, { "nct_id": "NCT00796055", "title": "Study of MEDI-547 to Evaluate the Safety, Tolerability, and Biologic Activity of IV Administration in Subjects With Relapsed or Refractory Solid Tumors", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Cancer" ], "interventions": [ { "name": "MEDI-547", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "MedImmune LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6, "start_date": "2009-08", "completion_date": "2010-06", "has_results": false, "last_update_posted_date": "2011-11-17", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 2, "location_summary": "Bethesda, Maryland • Detroit, Michigan", "locations": [ { "city": "Bethesda", "state": "Maryland" }, { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT00796055" }, { "nct_id": "NCT03843814", "title": "Pilot Study Using Amide Proton Transfer Magnetic Resonance Imaging Distinguishing Glioma", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Gliosarcoma", "Glioma" ], "interventions": [ { "name": "APT MRI", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 13, "start_date": "2014-08", "completion_date": "2017-12-13", "has_results": false, "last_update_posted_date": "2019-11-26", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT03843814" }, { "nct_id": "NCT02840084", "title": "Aspen™ Ultrasound System and Aspen Rehabilitation Technique in the Treatment of Capsular Contracture", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Capsular Contracture of Breast, Grade III" ], "interventions": [ { "name": "Aspen(TM) Ultrasound System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Nina Naidu", "sponsor_class": "INDIV", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "FEMALE", "summary": "22 Years and older · Female only" }, "enrollment_count": 10, "start_date": "2019-09-15", "completion_date": "2021-06-10", "has_results": false, "last_update_posted_date": "2021-06-15", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02840084" }, { "nct_id": "NCT01369147", "title": "The Energy Dose Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Critical Illness" ], "interventions": [ { "name": "Parenteral Nutrition", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" }, { "name": "Clevidipine", "type": "DRUG" }, { "name": "Dextrose-containing IV Fluids", "type": "DRUG" }, { "name": "Enteral feeding", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 12, "start_date": "2011-07", "completion_date": "2014-12-02", "has_results": true, "last_update_posted_date": "2022-06-10", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01369147" }, { "nct_id": "NCT05014984", "title": "WOOP VA: Promoting Weight Management in Primary Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity" ], "interventions": [ { "name": "mental contrasting with implementation intentions", "type": "BEHAVIORAL" }, { "name": "telephone-delivered, telehealth-delivered, and or in-person MOVE! or TeleMOVE!", "type": "BEHAVIORAL" }, { "name": "Information About Diet, Physical Activity, and Weight Management (Baseline Visit - 10 minutes): All", "type": "BEHAVIORAL" }, { "name": "Telephone MCII Check-ins (30 minutes at 3 days, 4 weeks, and 2 months after baseline visit)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 405, "start_date": "2022-02-15", "completion_date": "2026-02-11", "has_results": false, "last_update_posted_date": "2026-05-20", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05014984" }, { "nct_id": "NCT01948349", "title": "Impact of Bracket Design and Oral Hygiene Maintenance on Halitosis in the Orthodontic Patient", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Halitosis", "Oral Hygiene" ], "interventions": [ { "name": "Tongue scraping", "type": "OTHER" }, { "name": "Bracket design", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "UConn Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "11 Years", "maximum_age": "16 Years", "sex": "ALL", "summary": "11 Years to 16 Years" }, "enrollment_count": 40, "start_date": "2012-10", "completion_date": "2016-09", "has_results": false, "last_update_posted_date": "2019-12-13", "last_synced_at": "2026-10-20T03:04:19.223Z", "location_count": 1, "location_summary": "Farmington, Connecticut", "locations": [ { "city": "Farmington", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT01948349" } ] }