{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+Delivery+Format&page=2", "query": { "intervention": "Standard Delivery Format", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+Delivery+Format&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-20T14:34:04.496Z", "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": "NCT06275412", "title": "Family Intervention for Black Teens With Type 1 Diabetes", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 1 Diabetes", "Family Relations" ], "interventions": [ { "name": "The 3Ms 2.0 Intervention", "type": "BEHAVIORAL" }, { "name": "Educational Attention Control (EAC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Wayne State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "10 Years", "maximum_age": "14 Years", "sex": "ALL", "summary": "10 Years to 14 Years" }, "enrollment_count": 216, "start_date": "2024-09-16", "completion_date": "2028-04-30", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 4, "location_summary": "Washington D.C., District of Columbia • Detroit, Michigan • Memphis, Tennessee", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Detroit", "state": "Michigan" }, { "city": "Memphis", "state": "Tennessee" }, { "city": "Memphis", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT06275412" }, { "nct_id": "NCT03800238", "title": "Telehealth Powerful Tools for Caregivers Effectiveness Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Caregivers" ], "interventions": [ { "name": "Telehealth Delivery Format", "type": "BEHAVIORAL" }, { "name": "Standard Delivery Format", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Concordia University Wisconsin", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 115, "start_date": "2019-02-01", "completion_date": "2020-10-08", "has_results": false, "last_update_posted_date": "2020-10-29", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 12, "location_summary": "Los Angeles, California • Santa Cruz, California • Tampa, Florida + 9 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Santa Cruz", "state": "California" }, { "city": "Tampa", "state": "Florida" }, { "city": "Pocatello", "state": "Idaho" }, { "city": "Webster City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT03800238" }, { "nct_id": "NCT05751473", "title": "Reducing Posttraumatic Stress Disorder (PTSD) Symptoms in First Responders and Frontline Health Care Workers", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post Traumatic Stress Disorder" ], "interventions": [ { "name": "Prolonged Exposure for Primary Care (PE-PC)", "type": "BEHAVIORAL" }, { "name": "EAP Treatment as Usual (TAU)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 410, "start_date": "2023-05-16", "completion_date": "2027-07-30", "has_results": false, "last_update_posted_date": "2026-07-01", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 14, "location_summary": "San Diego, California • Carrollton, Georgia • Ann Arbor, Michigan + 9 more", "locations": [ { "city": "San Diego", "state": "California" }, { "city": "Carrollton", "state": "Georgia" }, { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Detroit", "state": "Michigan" }, { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05751473" }, { "nct_id": "NCT00397930", "title": "Yoga in Treating Sleep Disturbance in Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Fatigue", "Cancer", "Sleep Disorders" ], "interventions": [ { "name": "Standard Care Control Condition", "type": "PROCEDURE" }, { "name": "Yoga Intervention (YOCAS)", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Gary Morrow", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "21 Years to 120 Years" }, "enrollment_count": 410, "start_date": "2006-10", "completion_date": "2013-06", "has_results": true, "last_update_posted_date": "2017-02-20", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 11, "location_summary": "Decatur, Illinois • Wichita, Kansas • Grand Rapids, Michigan + 8 more", "locations": [ { "city": "Decatur", "state": "Illinois" }, { "city": "Wichita", "state": "Kansas" }, { "city": "Grand Rapids", "state": "Michigan" }, { "city": "Kalamazoo", "state": "Michigan" }, { "city": "Kansas City", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT00397930" }, { "nct_id": "NCT04933851", "title": "ACT1VATE: Addressing Emotional Distress to Improve Outcomes Among Diverse Adults With Type 1 Diabetes", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Type 1 Diabetes" ], "interventions": [ { "name": "ACT1VATE", "type": "BEHAVIORAL" }, { "name": "DSME/S", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Scripps Whittier Diabetes Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2021-10-25", "completion_date": "2027-03-31", "has_results": false, "last_update_posted_date": "2026-05-29", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04933851" }, { "nct_id": "NCT01918774", "title": "Cognitive Behavior Therapy for Work Success in Veterans With Mental Illness: A Pre-post Efficacy Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mental Disorders", "Mental Health Services" ], "interventions": [ { "name": "Cognitive behavior therapy for work success (CBTw)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 57, "start_date": "2016-02-01", "completion_date": "2018-09-30", "has_results": true, "last_update_posted_date": "2019-08-19", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT01918774" }, { "nct_id": "NCT07552857", "title": "A Vaccine Communication Training Intervention for Pediatric Inpatient Clinicians", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Preventive Health Services (PREV HEALTH SERV)" ], "interventions": [ { "name": "PIVOT-IN", "type": "BEHAVIORAL" }, { "name": "Standardized Vaccine Eligibility Screening", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Seattle Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 2000, "start_date": "2026-04", "completion_date": "2027-02", "has_results": false, "last_update_posted_date": "2026-05-05", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT07552857" }, { "nct_id": "NCT06817473", "title": "Evaluation of the Feasibility and Efficacy of Computerized Anxiety Treatment in a Group Setting", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Computerized Anxiety Sensitivity Treatment", "Health Education Treatment" ], "interventions": [ { "name": "CAST", "type": "BEHAVIORAL" }, { "name": "HET", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Florida State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 73, "start_date": "2024-02-21", "completion_date": "2025-01-15", "has_results": false, "last_update_posted_date": "2025-02-10", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 1, "location_summary": "Tallahassee, Florida", "locations": [ { "city": "Tallahassee", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06817473" }, { "nct_id": "NCT01688427", "title": "Perinatal Nurse Home Visiting Enhanced With mHealth Technology", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Domestic Violence", "Intimate Partner Violence" ], "interventions": [ { "name": "Standard IPV Assessment", "type": "BEHAVIORAL" }, { "name": "Standard DOVE Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "15 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "15 Years to 45 Years · Female only" }, "enrollment_count": 433, "start_date": "2012-10", "completion_date": "2018-09-30", "has_results": false, "last_update_posted_date": "2019-03-06", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01688427" }, { "nct_id": "NCT07656545", "title": "Early Intervention to Prevent Development of PTSD in Burn Survivors and Their Caregivers", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Posttraumatic Stress Disorder", "Burns", "Traumatic Injury", "Acute Stress Disorder", "Trauma and Stressor Related Disorders", "Trauma and Stress Related Disorders", "Stress Disorder", "Stress Disorders, Post-Traumatic", "Stress Disorders, Traumatic", "Stress Disorders, Traumatic, Acute", "Relationship, Social" ], "interventions": [ { "name": "Promotion of Emotional Disclosure for Burns (PoED-B)", "type": "BEHAVIORAL" }, { "name": "minimally Enhanced Usual Care control (mEUC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Southern California", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 44, "start_date": "2026-08-01", "completion_date": "2029-02-28", "has_results": false, "last_update_posted_date": "2026-06-18", "last_synced_at": "2026-09-20T14:34:04.496Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07656545" } ] }