{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Electronic+Decision+Support", "query": { "intervention": "Electronic Decision Support" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 282, "total_pages": 29, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Electronic+Decision+Support&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-03T22:55:54.141Z", "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": "NCT03826758", "title": "Enhanced Dynamic Clinical Decision Support System Pragmatic Trial (E-DYNAMIC)", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Kidney Diseases" ], "interventions": [ { "name": "E-DYNAMIC Clinical Decision Support", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Loyola University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 8000, "start_date": "2021-01-01", "completion_date": "2023-09-30", "has_results": false, "last_update_posted_date": "2020-08-27", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Hines, Illinois", "locations": [ { "city": "Hines", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03826758" }, { "nct_id": "NCT07290361", "title": "Stratified Targeted Engagement From Primary Care to Physical Therapy (STEPPT)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Low Back Pain", "Neck Pain" ], "interventions": [ { "name": "Engagement of clinic leadership (System Intervention - Usual Care)", "type": "BEHAVIORAL" }, { "name": "Engagement of clinic leadership (System Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Patient Registry (System Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Delivery of Patient Education Materials (System Intervention - Usual Care)", "type": "BEHAVIORAL" }, { "name": "Delivery of Patient Education Materials (System Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Referral Specialist Training (System Intervention - Usual Care)", "type": "BEHAVIORAL" }, { "name": "Patient Health Navigator Training (System Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Care Navigation (System Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Care navigation audit and feedback (System Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Primary Care Provider training (Provider Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Nurse/Medical Assistant Training (Provider Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Provider feedback on PT referral and adherence (Provider Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Patient education on spine pain condition (Patient Intervention - Usual Care)", "type": "BEHAVIORAL" }, { "name": "Patient education on spine pain condition (Patient Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Patient Education on Physical Referral by Providers (Patient Intervention - Usual Care)", "type": "BEHAVIORAL" }, { "name": "Patient Education on Physical Referral by Providers (Patient Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Electronic Patient Education on Physical Therapy Referral (Patient Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Patient education on physical therapy referral by Referral Specialist (Patient Intervention - Usual Care)", "type": "BEHAVIORAL" }, { "name": "Patient education on physical therapy referral by Patient Health Navigator (Patient Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Care Navigation (System Intervention - Usual Care)", "type": "BEHAVIORAL" }, { "name": "Monitoring of PT referral and adherence rates (System Intervention - STEPPT)", "type": "BEHAVIORAL" }, { "name": "Monitoring of PT referral and adherence rates (System intervention - Usual Care)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "San Diego State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 17587, "start_date": "2025-12-01", "completion_date": "2029-02-28", "has_results": false, "last_update_posted_date": "2026-08-14", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07290361" }, { "nct_id": "NCT02779725", "title": "SymptomCare@Home: Deconstructing an Effective Symptom Management Intervention", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer" ], "interventions": [ { "name": "SCC", "type": "BEHAVIORAL" }, { "name": "Nurse Practitioner", "type": "BEHAVIORAL" }, { "name": "DSS", "type": "BEHAVIORAL" }, { "name": "AT", "type": "BEHAVIORAL" }, { "name": "Symptom Severity", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 884, "start_date": "2017-08-07", "completion_date": "2022-09-30", "has_results": false, "last_update_posted_date": "2023-11-08", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT02779725" }, { "nct_id": "NCT03169868", "title": "Enhanced Medication Reconciliation For Serious Mental Illness", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mental Disorders" ], "interventions": [ { "name": "Sano Patient Medication Profile", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Precera Bioscience, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 26, "start_date": "2018-02-27", "completion_date": "2019-01-21", "has_results": false, "last_update_posted_date": "2019-01-25", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03169868" }, { "nct_id": "NCT07352579", "title": "From Screening to Support: A Multi-Method Analysis of HRSN Integration in Cancer Care", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cancer" ], "interventions": [ { "name": "Survey", "type": "OTHER" }, { "name": "Interview", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Thomas Jefferson University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 500, "start_date": "2025-12-11", "completion_date": "2027-01", "has_results": false, "last_update_posted_date": "2026-02-12", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07352579" }, { "nct_id": "NCT00225628", "title": "Improving Quality With Outpatient Decision Support", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus", "Coronary Artery Disease", "Osteoporosis", "Hypertension", "Hyperlipidemia" ], "interventions": [ { "name": "Computerized Reminders Medications Monitoring", "type": "BEHAVIORAL" }, { "name": "Computerized Test Results Management Application", "type": "BEHAVIORAL" }, { "name": "Computerized Reminders Hypertension Management", "type": "BEHAVIORAL" }, { "name": "Computerized Reminders Osteoporosis Screening and Mgt", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Agency for Healthcare Research and Quality (AHRQ)", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3000, "start_date": "2000-09", "completion_date": "2006-12", "has_results": false, "last_update_posted_date": "2005-09-26", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00225628" }, { "nct_id": "NCT06654245", "title": "Assessing and Addressing Follow-up Care Needs That Will Facilitate Care Transitions for Cancer Survivors", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stage I Lung Cancer", "Stage II Lung Cancer", "Stage III Lung Cancer", "Stage IV Lung Cancer" ], "interventions": [ { "name": "Telephone based interview", "type": "BEHAVIORAL" }, { "name": "Survey using a questionnaire.", "type": "OTHER" }, { "name": "Electronic health record review", "type": "OTHER" }, { "name": "Referral", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 5, "start_date": "2025-06-11", "completion_date": "2026-01-12", "has_results": false, "last_update_posted_date": "2026-01-30", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06654245" }, { "nct_id": "NCT05351749", "title": "Implementing Prescriber-Pharmacist Collaborative Care for Evidence-based Anticoagulant Use", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pulmonary Embolism", "Venous Thromboembolism", "Atrial Fibrillation" ], "interventions": [ { "name": "New-prescription Alert", "type": "BEHAVIORAL" }, { "name": "New-prescription Alert with referral option", "type": "BEHAVIORAL" }, { "name": "Existing-prescription notification to prescriber", "type": "BEHAVIORAL" }, { "name": "Existing-prescription notification to pharmacist", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 306, "start_date": "2022-08-01", "completion_date": "2024-12-15", "has_results": true, "last_update_posted_date": "2026-03-30", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05351749" }, { "nct_id": "NCT07598721", "title": "Ambient AI Clinical Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Artificial Intelligence (AI)", "Physician Burnout", "Physician Work Environment" ], "interventions": [ { "name": "Use of Ambient AI scribe tool on participant's mobile device", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 139, "start_date": "2024-12-19", "completion_date": "2025-07-04", "has_results": false, "last_update_posted_date": "2026-05-28", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT07598721" }, { "nct_id": "NCT07124728", "title": "Syntrillo Telehealth Stroke Risk Reduction Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension", "Hypertension (HTN)", "Stroke Prevention", "Cardiovascular Risk Factor" ], "interventions": [ { "name": "Technology-enabled Telehealth Care Plan", "type": "BEHAVIORAL" }, { "name": "Blood Pressure Monitoring Device", "type": "DEVICE" }, { "name": "Tenovi Smart Pillbox", "type": "DEVICE" }, { "name": "Wearable Activity Trackers (Fitbit or Apple Watch)", "type": "DEVICE" }, { "name": "Healthie EHR", "type": "OTHER" }, { "name": "Secure Messaging Platforms (TigerConnect, Weave, AirCall)", "type": "OTHER" }, { "name": "Antihypertensive Medication Management", "type": "DRUG" }, { "name": "Statin Medication Management", "type": "DRUG" }, { "name": "Antiplatelet or Anticoagulant Therapy", "type": "DRUG" }, { "name": "Laboratory Blood Test Collection", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE", "OTHER", "DRUG", "PROCEDURE" ], "sponsor": "Syntrillo, Inc", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": null, "sex": "ALL", "summary": "30 Years and older" }, "enrollment_count": 11, "start_date": "2025-07-30", "completion_date": "2026-07-22", "has_results": false, "last_update_posted_date": "2026-07-30", "last_synced_at": "2026-09-03T22:55:54.141Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07124728" } ] }