{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Developmental+Screening&page=9", "query": { "intervention": "Developmental Screening", "page": 9 }, "page_size": 10 }, "pagination": { "page": 9, "page_size": 10, "total_count": 296, "total_pages": 30, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Developmental+Screening&page=10&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Developmental+Screening&page=8&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-25T05:50:34.599Z", "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": "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": "2026-10-25T05:50:34.599Z", "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": "NCT04330131", "title": "TMW Community-Wide Demonstration Project", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Language Development" ], "interventions": [ { "name": "3Ts - Newborn", "type": "BEHAVIORAL" }, { "name": "3Ts - Well Baby", "type": "BEHAVIORAL" }, { "name": "3Ts - Let's Talk!", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "16 Years", "maximum_age": null, "sex": "ALL", "summary": "16 Years and older" }, "enrollment_count": 0, "start_date": "2021-12", "completion_date": "2023-12", "has_results": false, "last_update_posted_date": "2022-03-03", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 4, "location_summary": "West Palm Beach, Florida • Chicago, Illinois", "locations": [ { "city": "West Palm Beach", "state": "Florida" }, { "city": "West Palm Beach", "state": "Florida" }, { "city": "West Palm Beach", "state": "Florida" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04330131" }, { "nct_id": "NCT02423031", "title": "Checking Out Checking In: The Development and Validation of an Electronic Screening Tool for Pediatric Psychosocial Distress", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cancer" ], "interventions": [], "intervention_types": [], "sponsor": "National Institute of Mental Health (NIMH)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "8 Years to 21 Years" }, "enrollment_count": 178, "start_date": "2015-04-14", "completion_date": "2021-11-10", "has_results": false, "last_update_posted_date": "2025-05-31", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 4, "location_summary": "Aurora, Colorado • Baltimore, Maryland • Bethesda, Maryland + 1 more", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "Bethesda", "state": "Maryland" }, { "city": "Charlotte", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02423031" }, { "nct_id": "NCT03673566", "title": "Clinical Evaluation of the \"NICU Clinical Decision Support Dashboard\" - CHMCO", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Preterm Birth", "Low; Birthweight, Extremely (999 Grams or Less)", "Neonatal Infection", "Satisfaction", "Stress", "Chronic Lung Disease", "Growth Acceleration", "Adverse Event" ], "interventions": [ { "name": "NICU Dashboard", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Philips Healthcare", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 0, "start_date": "2019-03-20", "completion_date": "2020-04-01", "has_results": false, "last_update_posted_date": "2020-09-24", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 1, "location_summary": "Omaha, Nebraska", "locations": [ { "city": "Omaha", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT03673566" }, { "nct_id": "NCT02598050", "title": "Preoperative Cognitive Screening in Older Surgical Patients Utility for Predicting Morbidity", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cognitive Impairment" ], "interventions": [ { "name": "No Interventions as this is a observational study", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Brigham and Women's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 250, "start_date": "2016-02-01", "completion_date": "2017-12-31", "has_results": false, "last_update_posted_date": "2021-04-15", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT02598050" }, { "nct_id": "NCT01852708", "title": "Development of Non-invasive Prenatal Screening Test for Microdeletions Based on Fetal DNA Isolated From Maternal Blood", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Trisomy 21", "Trisomy 18", "Trisomy 13", "Sex Chromosome Abnormalities", "Microdeletion Syndromes" ], "interventions": [], "intervention_types": [], "sponsor": "Natera, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1059, "start_date": "2012-11", "completion_date": "2020-10", "has_results": false, "last_update_posted_date": "2020-12-30", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 7, "location_summary": "San Carlos, California • San Gabriel, California • Washington D.C., District of Columbia + 4 more", "locations": [ { "city": "San Carlos", "state": "California" }, { "city": "San Gabriel", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "New Brunswick", "state": "New Jersey" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01852708" }, { "nct_id": "NCT04674033", "title": "The Sweet PEA Study: Effects of Diet During Pregnancy on Infant Growth and Development.", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Obesity" ], "interventions": [], "intervention_types": [], "sponsor": "University of Southern California", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "FEMALE", "summary": "18 Years to 40 Years · Female only" }, "enrollment_count": 93, "start_date": "2019-01-18", "completion_date": "2020-07-01", "has_results": false, "last_update_posted_date": "2024-12-06", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04674033" }, { "nct_id": "NCT05857969", "title": "Ex Vivo Drug Sensitivity Testing and Multi-Omics Profiling", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Recurrent Childhood Acute Myeloid Leukemia", "Recurrent Childhood Acute Lymphoblastic Leukemia", "Recurrent Childhood Large Cell Lymphoma", "Refractory Childhood Acute Lymphoblastic Leukemia", "Refractory Childhood Hodgkin Lymphoma", "Refractory Childhood Malignant Germ Cell Neoplasm", "Recurrent Childhood Brain Tumor", "Recurrent Childhood Brainstem Glioma", "Recurrent Childhood Rhabdomyosarcoma", "Recurrent Childhood Soft Tissue Sarcoma", "Recurrent Childhood Ependymoma", "Recurrent Childhood Lymphoblastic Lymphoma", "Recurrent Childhood Gliosarcoma", "Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "Refractory Childhood Malignant Solid Neoplasm", "Recurrent Childhood Malignant Solid Neoplasm", "Recurrent Childhood Malignant Neoplasm", "Refractory Childhood Malignant Neoplasm" ], "interventions": [ { "name": "Functional Precision Medicine", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Florida International University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Day", "maximum_age": "21 Years", "sex": "ALL", "summary": "1 Day to 21 Years" }, "enrollment_count": 65, "start_date": "2023-02-22", "completion_date": "2028-12-31", "has_results": false, "last_update_posted_date": "2026-08-26", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05857969" }, { "nct_id": "NCT04586452", "title": "NIH CCR2 AAA Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Abdominal Aortic Aneurysm (AAA)", "No Abdominal Aortic Aneurysm (Non-AAA)" ], "interventions": [ { "name": "AAA Group (Aim 3A)", "type": "DIAGNOSTIC_TEST" }, { "name": "Non-AAA Group", "type": "DIAGNOSTIC_TEST" }, { "name": "Ex Vivo Human AAA Specimens (Aim 2A)", "type": "OTHER" }, { "name": "Relationship between radiotracer and CCR2 (Aim 2B)", "type": "OTHER" }, { "name": "AAA Group (Aim 3B-Reproducibility)", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 50, "start_date": "2021-02-17", "completion_date": "2022-04-04", "has_results": false, "last_update_posted_date": "2025-07-15", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04586452" }, { "nct_id": "NCT04740060", "title": "Effects of Different Types of Augmented Feedback on Intrinsic Motivation and Spatiotemporal Gait Performance After Stroke", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Hemiparesis", "Walking, Difficulty" ], "interventions": [ { "name": "Augmented Feedback without Virtual Reality(VR", "type": "OTHER" }, { "name": "Augmented Feedback with Non-Game based VR", "type": "OTHER" }, { "name": "Augmented Feedback with Game based VR", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 18, "start_date": "2021-07-10", "completion_date": "2022-05-01", "has_results": false, "last_update_posted_date": "2022-05-17", "last_synced_at": "2026-10-25T05:50:34.599Z", "location_count": 2, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT04740060" } ] }