{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Cognitive+testing&page=10", "query": { "intervention": "Cognitive testing", "page": 10 }, "page_size": 10 }, "pagination": { "page": 10, "page_size": 10, "total_count": 1070, "total_pages": 107, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Cognitive+testing&page=11&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Cognitive+testing&page=9&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-18T05:10:20.962Z", "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": "NCT06436209", "title": "Cognitive Control & the Functional Organization of the Frontal Cortex", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Multitasking Behavior and Neural Representations Associated With Multitasking Ability", "Healthy Volunteers", "Executive Function" ], "interventions": [ { "name": "Multitask Practice Intervention (MPI)", "type": "BEHAVIORAL" }, { "name": "Single-task Practice Intervention (SPI)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Brown University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "18 Years to 35 Years" }, "enrollment_count": 60, "start_date": "2024-03-27", "completion_date": "2026-07-31", "has_results": false, "last_update_posted_date": "2025-08-15", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "Providence, Rhode Island", "locations": [ { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT06436209" }, { "nct_id": "NCT05886400", "title": "The Effects of Environmental Distractions on SCAT6 Outcomes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Concussion, Brain", "Mild Traumatic Brain Injury" ], "interventions": [ { "name": "SCAT6", "type": "OTHER" }, { "name": "Visual/ Auditory Distraction", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "18 Years to 30 Years" }, "enrollment_count": 48, "start_date": "2023-09-01", "completion_date": "2024-05-01", "has_results": false, "last_update_posted_date": "2024-06-24", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "Bloomington, Indiana", "locations": [ { "city": "Bloomington", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT05886400" }, { "nct_id": "NCT00938665", "title": "Evaluation of a Handheld Event Related Potential (ERP)/Quantitative Electroencephalography (qEEG) System (COGNISION™) as a Useful Cognitive Biomarker for Alzheimer's Disease.", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Memory Disorders", "Alzheimer Disease", "Dementia", "Cognitive Impairment", "Frontotemporal Dementia" ], "interventions": [ { "name": "COGNISION™ System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Neuronetrix, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "60 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "60 Years to 90 Years" }, "enrollment_count": 204, "start_date": "2010-12", "completion_date": "2014-02", "has_results": false, "last_update_posted_date": "2014-03-10", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 7, "location_summary": "West Palm Beach, Florida • Lexington, Kentucky • Louisville, Kentucky + 4 more", "locations": [ { "city": "West Palm Beach", "state": "Florida" }, { "city": "Lexington", "state": "Kentucky" }, { "city": "Louisville", "state": "Kentucky" }, { "city": "Brookline", "state": "Massachusetts" }, { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00938665" }, { "nct_id": "NCT04106011", "title": "Cognitive Changes With Gabapentin Treatment", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Neuralgia Peripheral", "Pain" ], "interventions": [ { "name": "Gabapentin", "type": "DRUG" }, { "name": "BTACT", "type": "DIAGNOSTIC_TEST" }, { "name": "BPI", "type": "DIAGNOSTIC_TEST" }, { "name": "HADS", "type": "DIAGNOSTIC_TEST" }, { "name": "SLP9", "type": "DIAGNOSTIC_TEST" }, { "name": "NPSI", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DRUG", "DIAGNOSTIC_TEST" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 3, "start_date": "2020-01-10", "completion_date": "2021-02-18", "has_results": false, "last_update_posted_date": "2021-03-01", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04106011" }, { "nct_id": "NCT07805044", "title": "Truway Whole-Body Digital Twin and Physiologic Resilience Study (TRU-OMNIBODY)", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "PHYSIOLOGICAL PHENOMENA", "Homeostasis", "Physical Functional Performance", "Cardiorespiratory Fitness", "Cardiometabolic Risk Factors", "Mobility Limitation" ], "interventions": [ { "name": "Standardized Physiologic Resilience Challenge", "type": "PROCEDURE" }, { "name": "Multimodal Whole-Body Physiologic Monitoring", "type": "OTHER" }, { "name": "Research-Only Whole-Body Digital Twin Analysis", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Truway Health, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 450, "start_date": "2026-08-31", "completion_date": "2041-06-30", "has_results": false, "last_update_posted_date": "2026-09-04", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07805044" }, { "nct_id": "NCT01336309", "title": "Development of a Translational Tool to Study Yoga Therapy", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Health Behavior" ], "interventions": [ { "name": "Yoga Research Tool", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Connecticut", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 1832, "start_date": "2011-01", "completion_date": "2016-08", "has_results": false, "last_update_posted_date": "2016-08-10", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "Storrs, Connecticut", "locations": [ { "city": "Storrs", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT01336309" }, { "nct_id": "NCT02488863", "title": "NEPAL (Neuromodulatory Examination of Pain and Mobility Across the Lifespan)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Musculoskeletal Pain", "Pain, Chronic" ], "interventions": [ { "name": "MRI Neuroimaging", "type": "OTHER" }, { "name": "Quantitative Sensory Testing", "type": "OTHER" }, { "name": "Questionnaires", "type": "OTHER" }, { "name": "Physical and Cognitive Function Testing", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 105, "start_date": "2015-07", "completion_date": "2024-02-04", "has_results": true, "last_update_posted_date": "2025-03-18", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 4, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Gainesville", "state": "Florida" }, { "city": "Gainesville", "state": "Florida" }, { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02488863" }, { "nct_id": "NCT03304587", "title": "Effects of Bright Light on Co-occurring Cancer-related Symptoms in Breast Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Polysomnography (PSG)", "type": "DIAGNOSTIC_TEST" }, { "name": "Rectal thermistor 400 Series", "type": "DIAGNOSTIC_TEST" }, { "name": "Bright blue-green light", "type": "OTHER" }, { "name": "Dim red light", "type": "OTHER" }, { "name": "Digital foot candle datalogging light meter", "type": "DIAGNOSTIC_TEST" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Cancer-Fatigue", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Sleep Disturbance", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Depression", "type": "OTHER" }, { "name": "Patient-Reported Outcomes Measurement Information System (PROMIS)-Physical Function", "type": "OTHER" }, { "name": "Pittsburgh Sleep Quality Index (PSQI)", "type": "OTHER" }, { "name": "Center for Epidemiological Studies - Depression", "type": "OTHER" }, { "name": "Montreal Cognitive Assessment (MoCA)", "type": "OTHER" }, { "name": "European Organization for Research and Treatment of Cancer-Quality of Life Questionnaire (EORTC QLQ-C30)", "type": "OTHER" }, { "name": "Daily Log", "type": "OTHER" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER" ], "sponsor": "Michigan State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 30, "start_date": "2017-11-06", "completion_date": "2022-08-31", "has_results": true, "last_update_posted_date": "2025-06-10", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "East Lansing, Michigan", "locations": [ { "city": "East Lansing", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03304587" }, { "nct_id": "NCT06782360", "title": "Cognitive Augmentation Via Multimodal Sensing and Auricular Neurostimulation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Healthy", "Cognitive Change", "Effects of External Neurostimulation on Cognition" ], "interventions": [ { "name": "Active Neurostimulation", "type": "DEVICE" }, { "name": "Sham Stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "OpenBCI", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 45, "start_date": "2025-04-30", "completion_date": "2026-03-15", "has_results": false, "last_update_posted_date": "2026-04-06", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "Brooklyn, New York", "locations": [ { "city": "Brooklyn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06782360" }, { "nct_id": "NCT02606591", "title": "Houston Independent School District (HISD) Yoga Evaluation", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Health and Wellness" ], "interventions": [ { "name": "Electroencephalograph", "type": "PROCEDURE" }, { "name": "Cognitive Tests", "type": "BEHAVIORAL" }, { "name": "Hair Sample", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "BEHAVIORAL", "OTHER" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "8 Years", "maximum_age": "11 Years", "sex": "ALL", "summary": "8 Years to 11 Years" }, "enrollment_count": 5, "start_date": "2016-03-31", "completion_date": "2018-02-20", "has_results": false, "last_update_posted_date": "2018-10-31", "last_synced_at": "2026-10-18T05:10:20.962Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02606591" } ] }