{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Upright+positioning&page=2", "query": { "intervention": "Upright positioning", "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=Upright+positioning&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-22T02:17:09.928Z", "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": "NCT07025421", "title": "The ARISE Study - Use of Vertical Positioning", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Respiratory Distress Syndrome" ], "interventions": [ { "name": "Intervention Upright Bed positioning", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 40, "start_date": "2025-08-25", "completion_date": "2028-08-31", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT07025421" }, { "nct_id": "NCT03024333", "title": "Effect of Different Viscous Foods and Liquids on Swallowing Sounds", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Deglutition Disorder" ], "interventions": [], "intervention_types": [], "sponsor": "University of Nebraska", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "19 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "19 Years to 60 Years" }, "enrollment_count": 30, "start_date": "2017-05-08", "completion_date": "2018-09-17", "has_results": false, "last_update_posted_date": "2023-09-15", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "Omaha, Nebraska", "locations": [ { "city": "Omaha", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT03024333" }, { "nct_id": "NCT04207333", "title": "Combined Effects of Prolonged Sitting and Mental Stress on the Cardiovascular System", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sedentary Behavior", "Cardiovascular Risk Factor", "Mental Stress", "Cognitive Change", "Cerebrovascular Insufficiency" ], "interventions": [ { "name": "Mental Arithmetic Test", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "35 Years", "maximum_age": "59 Years", "sex": "ALL", "summary": "35 Years to 59 Years" }, "enrollment_count": 6, "start_date": "2020-01-11", "completion_date": "2020-06-01", "has_results": true, "last_update_posted_date": "2023-04-18", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04207333" }, { "nct_id": "NCT05304416", "title": "Clinical Markers of Dysphagia in Cardiac Surgical Patients", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cardiovascular Diseases", "Dysphagia" ], "interventions": [ { "name": "Fiberoptic Endoscopic Evaluation of Swallowing", "type": "DIAGNOSTIC_TEST" }, { "name": "Simultaneous FEES and Videofluoroscopy instrumental swallowing exam", "type": "DIAGNOSTIC_TEST" }, { "name": "Videofluoroscopy instrumental swallowing exam (VFSS)", "type": "DIAGNOSTIC_TEST" }, { "name": "Voluntary Cough Peak Expiratory Flow (PEF) Testing", "type": "OTHER" }, { "name": "Reflex Cough Screen", "type": "OTHER" }, { "name": "Lingual Pressure Testing", "type": "OTHER" }, { "name": "Speech Testing", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER" ], "sponsor": "University of Florida", "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": 347, "start_date": "2022-06-07", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-08-06", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 2, "location_summary": "Gainesville, Florida • Columbus, Ohio", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05304416" }, { "nct_id": "NCT04301986", "title": "Patient Acceptance and Preference Among Screening Modalities for Detection of Barrett's Esophagus", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Barrett Esophagus", "GERD" ], "interventions": [ { "name": "Cytosponge", "type": "DEVICE" }, { "name": "Transnasal Endoscopy (TNE)", "type": "DEVICE" }, { "name": "Esophagogastroduodenoscopy", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 24, "start_date": "2020-08-11", "completion_date": "2022-05-10", "has_results": true, "last_update_posted_date": "2023-05-08", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04301986" }, { "nct_id": "NCT00975780", "title": "A Trial to Reduce Pneumonia in Nursing Home Residents", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Pneumonia", "Lower Respiratory Tract Infection" ], "interventions": [ { "name": "Enhanced Oral Care", "type": "OTHER" }, { "name": "Usual oral care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 834, "start_date": "2009-10", "completion_date": "2012-12", "has_results": true, "last_update_posted_date": "2014-11-20", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT00975780" }, { "nct_id": "NCT03862027", "title": "Safety of Optimal PEEP in NSICU Patients", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Respiratory Failure", "Intracranial Hypertension" ], "interventions": [ { "name": "Esophageal Balloon catheter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 1, "start_date": "2019-03-01", "completion_date": "2019-03-04", "has_results": true, "last_update_posted_date": "2021-04-27", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03862027" }, { "nct_id": "NCT04879862", "title": "Locomotor and Bladder Function in Individuals With Acute Spinal Cord Injury", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries" ], "interventions": [ { "name": "Epidural stimulation + Stand Training", "type": "COMBINATION_PRODUCT" }, { "name": "Epidural stimulation + Step Training", "type": "COMBINATION_PRODUCT" }, { "name": "Epidural stimulation + Bladder Capacity Training", "type": "COMBINATION_PRODUCT" }, { "name": "Epidural stimulation + Bladder Voiding Efficiency Training", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "Claudia Angeli", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 16, "start_date": "2022-04-04", "completion_date": "2029-04-28", "has_results": false, "last_update_posted_date": "2026-05-04", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "West Orange, New Jersey", "locations": [ { "city": "West Orange", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT04879862" }, { "nct_id": "NCT06763549", "title": "COR-INSIGHT: Optimizing Cardiovascular and Cardiopulmonary Outcomes with AI-Driven Multiplexed Indications Using COR ECG Wearable", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cardiopulmonary Failure", "Myocardial Infarction (MI)", "Heart Decompensation", "Heart Failure", "HFrEF - Heart Failure with Reduced Ejection Fraction", "HFpEF - Heart Failure with Preserved Ejection Fraction", "Syncopation", "Syncope", "Ischemic Cardiovascular Disease", "STEMI", "STEMI (ST Elevation MI)", "Atrial Fibrillation (AF)", "Atrial Enlargement", "LVF", "Conduction Defect", "Conduction Abnormalities", "Heart Block", "Valvular Diseases", "Cardiac Output, Low", "Stroke Volume", "Stroke Volume Variation", "Hyperkalemia", "Hypercalcemia", "Hypocalcemia", "LV Dysfunction", "QT Prolongation", "Sudden Cardiac Death Due to Cardiac Arrhythmia", "Ventricular Arrhythmia", "Pacing", "Pacing Induced Dyssynchrony", "Silent Ischemia", "Pericarditis", "Sleep Related Breathing Disorder", "RSA", "Apnea, Obstructive", "Cardiac Output Measurement", "Respiratory Impedance", "CRT And/or ICD", "Infarction", "Cardiomyopathies, Primary", "Hypertrophy" ], "interventions": [ { "name": "SUBPROTOCOL A", "type": "DEVICE" }, { "name": "SUBPROTOCOL B", "type": "DEVICE" }, { "name": "SUBPROTOCOL C", "type": "DEVICE" }, { "name": "SUBPROTOCOL D", "type": "DEVICE" }, { "name": "SUBPROTOCOL E", "type": "DEVICE" }, { "name": "SUBPROTOCOL F", "type": "DEVICE" }, { "name": "SUBPROTOCOL G", "type": "DEVICE" }, { "name": "SUBPROTOCOL H", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Peerbridge Health, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15000, "start_date": "2024-11-16", "completion_date": "2026-04-15", "has_results": false, "last_update_posted_date": "2025-01-08", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "Melbourne, Florida", "locations": [ { "city": "Melbourne", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06763549" }, { "nct_id": "NCT05313217", "title": "Spine Position and Neural Sensitivity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sciatic Nerve", "Postural Lordosis", "Nerve Pain" ], "interventions": [ { "name": "Knee extension angle", "type": "DIAGNOSTIC_TEST" }, { "name": "Straight Leg Raise", "type": "DIAGNOSTIC_TEST" }, { "name": "Slump Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Extended slump test", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "University of Hartford", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 40, "start_date": "2022-03-28", "completion_date": "2022-07-31", "has_results": false, "last_update_posted_date": "2023-05-10", "last_synced_at": "2026-09-22T02:17:09.928Z", "location_count": 1, "location_summary": "West Hartford, Connecticut", "locations": [ { "city": "West Hartford", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT05313217" } ] }