{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Checklist&page=2", "query": { "intervention": "Checklist", "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=Checklist&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-07T07:01:37.940Z", "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": "NCT07071350", "title": "Randomized Controlled Trial of Treatment to Optimize Heart Rate Variability for Persistent Post-Concussion Symptoms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Autonomic Nervous System Disease", "Concussive Injury", "Mild Traumatic Brain Injury", "Post Traumatic Stress Disorder", "Persistent Post Concussion Syndrome" ], "interventions": [ { "name": "HRV Coherence Ratio", "type": "OTHER" }, { "name": "NSI", "type": "BEHAVIORAL" }, { "name": "Pittsburgh Sleep Quality Index (PSQI)", "type": "BEHAVIORAL" }, { "name": "Quantitative Sleep Measures", "type": "BEHAVIORAL" }, { "name": "Patient Global Impression of Change (PGIC)", "type": "BEHAVIORAL" }, { "name": "Cognitive Performance/NIH Toolbox Cognitive Battery", "type": "BEHAVIORAL" }, { "name": "Pain Interference/TBI-QoL Pain Interference Short-Form", "type": "OTHER" }, { "name": "Patient Health Questionnaire-9 (PHQ-9)", "type": "BEHAVIORAL" }, { "name": "PTSD Checklist for DSM-5 (PCL-5)", "type": "BEHAVIORAL" }, { "name": "HRV Biofeedback (HRV-B)", "type": "OTHER" }, { "name": "Psychoeducational (Edu) Comparator Intervention", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Virginia Commonwealth University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 148, "start_date": "2025-09-02", "completion_date": "2028-09", "has_results": false, "last_update_posted_date": "2025-09-17", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07071350" }, { "nct_id": "NCT03540771", "title": "Introducing Palliative Care (PC) Within the Treatment of End Stage Liver Disease (ESLD)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "End Stage Liver Disease", "Decompensated Cirrhosis of Liver" ], "interventions": [ { "name": "Palliative Care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Albert Einstein Healthcare Network", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 1494, "start_date": "2019-01-30", "completion_date": "2025-08-30", "has_results": true, "last_update_posted_date": "2025-12-02", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 19, "location_summary": "Birmingham, Alabama • Phoenix, Arizona • Fresno, California + 15 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Fresno", "state": "California" }, { "city": "Loma Linda", "state": "California" }, { "city": "West Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT03540771" }, { "nct_id": "NCT04068727", "title": "LEAVE Safe With DOACs", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiovascular Diseases", "Venous Thromboembolism", "Atrial Fibrillation", "Bleeding", "Stroke" ], "interventions": [ { "name": "Clinical Pharmacist Intervention", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Massachusetts, Worcester", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 561, "start_date": "2019-12-02", "completion_date": "2022-09-14", "has_results": false, "last_update_posted_date": "2024-02-20", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 1, "location_summary": "Worcester, Massachusetts", "locations": [ { "city": "Worcester", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04068727" }, { "nct_id": "NCT05480956", "title": "SIRI Checklist: An Integrated Hospital Model to Optimize HIV Prevention in Persons Who Inject Drugs", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infections", "Opioid-Related Disorders", "Pre-Exposure Prophylaxis (PrEP)" ], "interventions": [ { "name": "SIRI Checklist", "type": "BEHAVIORAL" }, { "name": "Enhanced Peer Recovery Coach", "type": "BEHAVIORAL" }, { "name": "SIRI Checklist + Enhanced Peer Recovery Coach", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Alabama at Birmingham", "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": "2022-10-11", "completion_date": "2025-07-01", "has_results": true, "last_update_posted_date": "2026-08-19", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT05480956" }, { "nct_id": "NCT00988962", "title": "Substance Abuse Treatment for High Risk Chronic Pain Patients on Opioid Therapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Substance Abuse" ], "interventions": [ { "name": "cognitive behavioral training", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Brigham and Women's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 84, "start_date": "2009-07", "completion_date": "2011-06", "has_results": false, "last_update_posted_date": "2011-06-27", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 1, "location_summary": "Chestnut Hill, Massachusetts", "locations": [ { "city": "Chestnut Hill", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00988962" }, { "nct_id": "NCT05272163", "title": "Brief Title: Project 4 Example: Mixed Hybrid Checklist", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Incidental Findings", "Visual Attention", "Visual Search", "Hybrid Search" ], "interventions": [ { "name": "Stimulus Type", "type": "BEHAVIORAL" }, { "name": "Target Presence", "type": "BEHAVIORAL" }, { "name": "Checklist", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Brigham and Women's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 12, "start_date": "2018-01-17", "completion_date": "2024-01-01", "has_results": false, "last_update_posted_date": "2025-02-19", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05272163" }, { "nct_id": "NCT07022717", "title": "A Universal Primary Care Based Intervention to Reduce Youth Overdose Risk", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Overdose" ], "interventions": [ { "name": "Brief youth overdose prevention education", "type": "BEHAVIORAL" }, { "name": "Information about Naloxone", "type": "OTHER" }, { "name": "Usual standard of care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Boston Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": null, "sex": "ALL", "summary": "13 Years and older" }, "enrollment_count": 22, "start_date": "2025-08-25", "completion_date": "2026-11", "has_results": false, "last_update_posted_date": "2026-08-07", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07022717" }, { "nct_id": "NCT05419245", "title": "Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Freeman-Burian Syndrome", "Freeman-Sheldon Syndrome", "Whistling Face Syndrome", "Sheldon-Hall Syndrome", "Freeman-Sheldon Syndrome Variant", "Arthrogryposis Distal Type 1", "Arthrogryposis Distal Type 3", "Gordon Syndrome" ], "interventions": [ { "name": "Guided Health History for Freeman-Burian Syndrome Questionnaire", "type": "OTHER" }, { "name": "Freeman-Burian syndrome Semi-Structured Quality of Life Interview", "type": "OTHER" }, { "name": "Medical Records Review", "type": "OTHER" }, { "name": "PTSD Checklist for DSM-5", "type": "OTHER" }, { "name": "Modified Flanagan Quality of Life Scale", "type": "OTHER" }, { "name": "Center for Epidemiologic Studies Depression Scale", "type": "OTHER" }, { "name": "Review of Systems", "type": "OTHER" }, { "name": "FACE-Q | Craniofacial - Appearance of the Face", "type": "OTHER" }, { "name": "FACE-Q | Craniofacial - Appearance Distress", "type": "OTHER" }, { "name": "FACE-Q | Craniofacial - Facial Function", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Dufresne, Craig, MD, PC", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 20, "start_date": "2022-06-01", "completion_date": "2023-12", "has_results": false, "last_update_posted_date": "2022-07-19", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 1, "location_summary": "Fairfax, Virginia", "locations": [ { "city": "Fairfax", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05419245" }, { "nct_id": "NCT04181294", "title": "Time Limited Trials to Reduce Non-Beneficial Intensive Care Unit Treatments", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Critical Illness", "Communication" ], "interventions": [ { "name": "Family meetings using time limited trials as default ICU communication and care planning approach", "type": "BEHAVIORAL" }, { "name": "Usual practice", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Lundquist Institute for Biomedical Innovation at Harbor-UCLA 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": 209, "start_date": "2017-08-01", "completion_date": "2019-12-31", "has_results": false, "last_update_posted_date": "2025-11-21", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 3, "location_summary": "Los Angeles, California • Sylmar, California • Torrance, California", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Sylmar", "state": "California" }, { "city": "Torrance", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04181294" }, { "nct_id": "NCT07075042", "title": "Comparing the Attentional Demands and Functional Outcomes in People With Transradial Amputation", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Amputation", "Prosthesis Use" ], "interventions": [ { "name": "Training with PRC", "type": "DEVICE" }, { "name": "Training with DC", "type": "DEVICE" }, { "name": "PRC Device use in community and home", "type": "DEVICE" }, { "name": "DC Device use in community and home", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Virginia Commonwealth University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 32, "start_date": "2026-07", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-06-08", "last_synced_at": "2026-09-07T07:01:37.940Z", "location_count": 2, "location_summary": "Austin, Texas • Richmond, Virginia", "locations": [ { "city": "Austin", "state": "Texas" }, { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07075042" } ] }