{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=INDEPENDENCE&page=13", "query": { "intervention": "INDEPENDENCE", "page": 13 }, "page_size": 10 }, "pagination": { "page": 13, "page_size": 10, "total_count": 1020, "total_pages": 102, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=INDEPENDENCE&page=14&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=INDEPENDENCE&page=12&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-27T01:10:45.088Z", "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": "NCT05826587", "title": "Cardiac Rehabilitation Mobile-Health Fall Risk Prevention Intervention", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiac Rehabilitation" ], "interventions": [ { "name": "Home-based, m-Health Delivered Physical Function Training", "type": "BEHAVIORAL" }, { "name": "Cardiac Rehabilitation & Exercise Prescription", "type": "BEHAVIORAL" }, { "name": "Connected mHealth mobile application", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 128, "start_date": "2023-10-09", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-01-20", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 2, "location_summary": "Scottsdale, Arizona • Jacksonville, Florida", "locations": [ { "city": "Scottsdale", "state": "Arizona" }, { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05826587" }, { "nct_id": "NCT04128514", "title": "Spectacle Independence and Overall Satisfaction With AcrySof® Panoptix® Toric Intraocular Lens", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cataract" ], "interventions": [ { "name": "Panoptix Toric", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Eye Center of North Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 15, "start_date": "2019-10-11", "completion_date": "2022-03-10", "has_results": false, "last_update_posted_date": "2022-04-01", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Panama City, Florida", "locations": [ { "city": "Panama City", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04128514" }, { "nct_id": "NCT03952637", "title": "A Phase 1/2 Study of Intravenous Gene Transfer With an AAV9 Vector Expressing Human Beta-galactosidase in Type I and Type II GM1 Gangliosidosis", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Lysosomal Diseases", "Gangliosidosis", "GM1" ], "interventions": [ { "name": "AAV9-GLB1", "type": "BIOLOGICAL" }, { "name": "Abdominal ultrasound", "type": "PROCEDURE" }, { "name": "Rituximab", "type": "DRUG" }, { "name": "Sirolimus", "type": "DRUG" }, { "name": "Methylprednisolone", "type": "DRUG" }, { "name": "Prednisone", "type": "DRUG" }, { "name": "Audiology assessment with ABR", "type": "DIAGNOSTIC_TEST" }, { "name": "Bone density scan (DEXA)", "type": "DIAGNOSTIC_TEST" }, { "name": "Electrocardiogram (EKG)", "type": "DIAGNOSTIC_TEST" }, { "name": "Echocardiogram", "type": "DIAGNOSTIC_TEST" }, { "name": "Electroencephalogram (EEG) awake and extended overnight", "type": "OTHER" }, { "name": "Laboratory tests", "type": "DIAGNOSTIC_TEST" }, { "name": "Lumbar puncture", "type": "PROCEDURE" }, { "name": "Brain MRI/MRS/fMRI", "type": "PROCEDURE" }, { "name": "Neurocognitive testing", "type": "BEHAVIORAL" }, { "name": "Neurology exam", "type": "OTHER" }, { "name": "PICC or other Central line placement", "type": "BEHAVIORAL" }, { "name": "Skeletal survey", "type": "PROCEDURE" }, { "name": "Skin biopsy", "type": "PROCEDURE" }, { "name": "Speech and modified barium swallow study", "type": "PROCEDURE" }, { "name": "Ophthalmology exam", "type": "PROCEDURE" } ], "intervention_types": [ "BIOLOGICAL", "PROCEDURE", "DRUG", "DIAGNOSTIC_TEST", "OTHER", "BEHAVIORAL" ], "sponsor": "National Human Genome Research Institute (NHGRI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "6 Months", "maximum_age": "12 Years", "sex": "ALL", "summary": "6 Months to 12 Years" }, "enrollment_count": 54, "start_date": "2019-08-19", "completion_date": "2030-01-01", "has_results": false, "last_update_posted_date": "2026-09-21", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT03952637" }, { "nct_id": "NCT02109419", "title": "Feasibility and Validity of A Novel Computer Based Battery of Assessments in the Elderly", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Computerized Assessment Feasibility and Validity" ], "interventions": [ { "name": "HHT-G", "type": "OTHER" }, { "name": "HHT-D", "type": "OTHER" }, { "name": "Geriatric Depression Scale (DGS)", "type": "OTHER" }, { "name": "MMSE", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Pennington Biomedical Research Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "60 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "60 Years to 85 Years" }, "enrollment_count": 57, "start_date": "2014-03", "completion_date": "2014-10", "has_results": true, "last_update_posted_date": "2019-09-06", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Baton Rouge, Louisiana", "locations": [ { "city": "Baton Rouge", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT02109419" }, { "nct_id": "NCT07136272", "title": "Detection of Sleep Stages and Arousals Using Neural Network Classifiers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Disordered Breathing (SDB)", "Sleep Apnea" ], "interventions": [ { "name": "SSAM", "type": "DEVICE" }, { "name": "Polysomnography", "type": "DIAGNOSTIC_TEST" }, { "name": "EnsoSleep", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "DIAGNOSTIC_TEST" ], "sponsor": "Pathway Medtech, LLC.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 72, "start_date": "2025-10-04", "completion_date": "2025-12-21", "has_results": false, "last_update_posted_date": "2026-09-16", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 3, "location_summary": "Burlingame, California • Irvine, California • La Jolla, California", "locations": [ { "city": "Burlingame", "state": "California" }, { "city": "Irvine", "state": "California" }, { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07136272" }, { "nct_id": "NCT06667102", "title": "Strategic and Interactive Signing Instruction", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Teaching Behaviors", "Sign Language Skills" ], "interventions": [ { "name": "Strategic and Interactive Signing Instruction", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "The University of Tennessee, Knoxville", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "4 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "4 Years to 99 Years" }, "enrollment_count": 150, "start_date": "2024-08-23", "completion_date": "2026-12-30", "has_results": false, "last_update_posted_date": "2024-10-31", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Knoxville, Tennessee", "locations": [ { "city": "Knoxville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT06667102" }, { "nct_id": "NCT01395329", "title": "Nebivolol and the Endothelin (ET)-1 System", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Prehypertension", "Hypertension" ], "interventions": [ { "name": "Nebivolol", "type": "DRUG" }, { "name": "Metoprolol", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Forearm Blood Flow (FBF) response to BQ-123 (100 mol/min)", "type": "OTHER" }, { "name": "FBF response to BQ-123 (100 nmol/min)+BQ-788(50 nmol/min)", "type": "OTHER" }, { "name": "FBF response to Acetylcholine", "type": "OTHER" }, { "name": "FBF response to Sodium Nitroprusside", "type": "OTHER" }, { "name": "FBF response to BQ-123+BQ-788+ACh", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of Colorado, Boulder", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "45 Years to 65 Years" }, "enrollment_count": 42, "start_date": "2011-05", "completion_date": "2016-12", "has_results": true, "last_update_posted_date": "2019-01-02", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Boulder, Colorado", "locations": [ { "city": "Boulder", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT01395329" }, { "nct_id": "NCT02227472", "title": "Working Memory and School Readiness in Preschool-Aged Children With Sickle Cell Disease", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Sickle Cell Disease" ], "interventions": [ { "name": "Evaluation of cognitive and pre-academic skills", "type": "OTHER" }, { "name": "Parent questionnaires", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "St. Jude Children's Research Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "48 Months", "maximum_age": "68 Months", "sex": "ALL", "summary": "48 Months to 68 Months" }, "enrollment_count": 84, "start_date": "2014-09-08", "completion_date": "2018-08-20", "has_results": false, "last_update_posted_date": "2018-09-12", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Memphis, Tennessee", "locations": [ { "city": "Memphis", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02227472" }, { "nct_id": "NCT05342701", "title": "The CHAMP ASP: Promoting Physical Activity & Health in Children", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Inactivity" ], "interventions": [ { "name": "Motor Skills Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "5 Years", "maximum_age": "8 Years", "sex": "ALL", "summary": "5 Years to 8 Years" }, "enrollment_count": 264, "start_date": "2022-12-01", "completion_date": "2026-08-31", "has_results": false, "last_update_posted_date": "2026-02-27", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05342701" }, { "nct_id": "NCT03138551", "title": "Examining Relationships Between Family Mealtime and Feeding Outcomes in Young Children With Sensory Food Aversions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Feeding Disorder of Infancy or Early Childhood" ], "interventions": [ { "name": "Mealtime PREP (Promoting Routines of Exploration and Play)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Months", "maximum_age": "60 Months", "sex": "ALL", "summary": "18 Months to 60 Months" }, "enrollment_count": 20, "start_date": "2015-10-11", "completion_date": "2018-10-01", "has_results": false, "last_update_posted_date": "2019-02-06", "last_synced_at": "2026-10-27T01:10:45.088Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03138551" } ] }