{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Usual+Care+Group+-+Outcome+Measures", "query": { "intervention": "Usual Care Group - Outcome Measures" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 22, "total_pages": 3, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Usual+Care+Group+-+Outcome+Measures&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-29T10:11:44.173Z", "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": "NCT06374238", "title": "Peer Support for Adolescents and Emerging Adults With Sickle Cell Pain", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain", "Sickle Cell Disease" ], "interventions": [ { "name": "CBT+ Health coach", "type": "BEHAVIORAL" }, { "name": "CBT w/o Health Coach ( self-guided)", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "16 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "16 Years to 30 Years" }, "enrollment_count": 470, "start_date": "2025-03-10", "completion_date": "2028-05", "has_results": false, "last_update_posted_date": "2026-01-07", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 14, "location_summary": "Mobile, Alabama • Los Angeles, California • Hartford, Connecticut + 10 more", "locations": [ { "city": "Mobile", "state": "Alabama" }, { "city": "Los Angeles", "state": "California" }, { "city": "Hartford", "state": "Connecticut" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06374238" }, { "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": "2026-09-22", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07071350" }, { "nct_id": "NCT03851458", "title": "Consumption of More Ideal Food Options (COMIDA: Consumo de Opciones Más Ideales De Alimentos)", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Overweight", "Obesity" ], "interventions": [ { "name": "Initial in-person individual diet and exercise counseling (N vs. Y)", "type": "BEHAVIORAL" }, { "name": "Thrice weekly diet and exercise text messages (N vs. Y)", "type": "BEHAVIORAL" }, { "name": "Weekly telephone support (N vs. Y)", "type": "BEHAVIORAL" }, { "name": "Self-monitoring tools (N vs. Y) (for diet and weight)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1785, "start_date": "2015-05-05", "completion_date": "2027-05", "has_results": false, "last_update_posted_date": "2026-07-06", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03851458" }, { "nct_id": "NCT06550401", "title": "A Study of the BREAST-Q REACT Tool for People Having Breast Surgery", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Conserving Surgery", "Mastectomy With Reconstruction" ], "interventions": [ { "name": "BREAST-Q Physical Well-Being", "type": "OTHER" }, { "name": "QuickDASH", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "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": 69, "start_date": "2024-08-09", "completion_date": "2027-08", "has_results": false, "last_update_posted_date": "2026-09-10", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 6, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Commack, New York + 3 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06550401" }, { "nct_id": "NCT04851184", "title": "Dose of Vestibular Rehabilitation for Vestibular Hypofunction", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vestibular Disorder" ], "interventions": [ { "name": "Gaze stabilization Exercises using Virtual Reality Device", "type": "DEVICE" }, { "name": "Gaze stabilization non-instrumented", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "74 Years", "sex": "ALL", "summary": "18 Years to 74 Years" }, "enrollment_count": 28, "start_date": "2021-03-22", "completion_date": "2024-09-01", "has_results": true, "last_update_posted_date": "2025-12-17", "last_synced_at": "2026-09-29T10:11:44.173Z", "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/NCT04851184" }, { "nct_id": "NCT05278806", "title": "Evaluating the Impact of an Equity Focused Dashboard and Clinical Support", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension", "Diabetes", "Breast Cancer" ], "interventions": [ { "name": "Equity Dashboard, Population Health Coordinator and Community Health Worker Support", "type": "OTHER" }, { "name": "Equity Dashboard and Population Health Coordinator Support", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 10766, "start_date": "2022-03-24", "completion_date": "2023-04-30", "has_results": false, "last_update_posted_date": "2023-06-26", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05278806" }, { "nct_id": "NCT04118569", "title": "Personalized Experiences to Inform Improved Communication for Patients With Life Limiting Illness", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Heart Failure", "Renal Failure" ], "interventions": [ { "name": "Narrative Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 51, "start_date": "2019-10-01", "completion_date": "2022-06-22", "has_results": false, "last_update_posted_date": "2023-04-10", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04118569" }, { "nct_id": "NCT03346161", "title": "Optimizing Decision Making About Breast Reconstruction After Mastectomy: A Patient-Centered Approach", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Usual care American Society of Plastic Surgeons booklet \"Breast Reconstruction\"", "type": "OTHER" }, { "name": "Decision tool", "type": "OTHER" }, { "name": "Usual Care Group - Outcome Measures", "type": "OTHER" }, { "name": "Decision Group - Outcome Measures", "type": "OTHER" }, { "name": "Demographic and Background Questions", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Washington University School of Medicine", "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": 120, "start_date": "2018-01-09", "completion_date": "2018-10-24", "has_results": true, "last_update_posted_date": "2019-09-06", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03346161" }, { "nct_id": "NCT05738330", "title": "Symptom Monitoring in Hemodialysis", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "End Stage Kidney Disease" ], "interventions": [ { "name": "Symptom Monitoring on Renal Replacement Therapy - Hemodialysis (SMaRRT-HD)", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2400, "start_date": "2023-06-24", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2025-11-24", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 1, "location_summary": "Waltham, Massachusetts", "locations": [ { "city": "Waltham", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05738330" }, { "nct_id": "NCT00579215", "title": "Lung Cancer Informational Study (LCIS)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Enhanced Care", "Decision-Making", "Advance Lung Cancer", "Stage III Lung Cancer", "Stage IV Lung Cancer" ], "interventions": [ { "name": "Enhance Care", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 8, "start_date": "2006-11", "completion_date": "2009-03", "has_results": false, "last_update_posted_date": "2009-03-18", "last_synced_at": "2026-09-29T10:11:44.173Z", "location_count": 2, "location_summary": "New York, New York • Charlottesville, Virginia", "locations": [ { "city": "New York", "state": "New York" }, { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT00579215" } ] }