{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+Cognitive+Techniques&page=2", "query": { "intervention": "Standard Cognitive Techniques", "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=Standard+Cognitive+Techniques&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-29T01:58:40.161Z", "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": "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": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07071350" }, { "nct_id": "NCT03208387", "title": "Understanding the Late Effects of Surviving a Pediatric Brain Tumor", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Brain Tumor", "Pediatric Brain Tumor", "Pediatric Cancer" ], "interventions": [ { "name": "Diffusion tensor imaging (DTI)", "type": "DIAGNOSTIC_TEST" }, { "name": "Resting state functional connectivity MRI (rs-fcMRI)", "type": "DIAGNOSTIC_TEST" }, { "name": "Wechsler Intelligence Scale for Children - 5th edition (WISC-V)", "type": "BEHAVIORAL" }, { "name": "California Verbal Learning Test (CVLT-C)", "type": "BEHAVIORAL" }, { "name": "Beery Test of Visual Motor Integration 6th edition", "type": "BEHAVIORAL" }, { "name": "Grooved Pegboard", "type": "BEHAVIORAL" }, { "name": "PedsQL Multidimensional Fatigue Scale", "type": "BEHAVIORAL" }, { "name": "MRI", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "6 Years", "maximum_age": "16 Years", "sex": "ALL", "summary": "6 Years to 16 Years" }, "enrollment_count": 42, "start_date": "2017-06-28", "completion_date": "2027-06", "has_results": false, "last_update_posted_date": "2026-07-02", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 4, "location_summary": "New York, New York • Dallas, Texas • Seattle, Washington", "locations": [ { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "Dallas", "state": "Texas" }, { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT03208387" }, { "nct_id": "NCT01019343", "title": "Physiological Investigations of Movement Disorders", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Parkinson's Disease", "Tourette's Syndrome", "Tic Disorders", "Dystonia", "Movement Disorders" ], "interventions": [ { "name": "Transcranial Direct Current Stimulation (tDCS)", "type": "PROCEDURE" }, { "name": "Eye-tracking Device", "type": "DEVICE" }, { "name": "Pulsed vibrator", "type": "DEVICE" }, { "name": "Gait Trainer Treadmill (GTT)", "type": "OTHER" }, { "name": "Standard psychiatric scales SCID-I, YBOCS and SCI-OBS-lifetime and cognitive scales MMSE and MOCA", "type": "OTHER" }, { "name": "iMobility", "type": "DEVICE" }, { "name": "QMAT", "type": "DEVICE" }, { "name": "Treadmill Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Arm Intellistretch Device", "type": "DEVICE" }, { "name": "Transcranial Sonography (TCS)", "type": "PROCEDURE" }, { "name": "Behavioral tasks", "type": "OTHER" }, { "name": "TMS single/paired pulse", "type": "PROCEDURE" }, { "name": "MEG", "type": "PROCEDURE" }, { "name": "EEG", "type": "PROCEDURE" }, { "name": "MRI techniques", "type": "PROCEDURE" }, { "name": "Peripheral Nerve Stimulation", "type": "PROCEDURE" }, { "name": "EMG", "type": "PROCEDURE" }, { "name": "Trancutaneous spinal direct current stimulation (tsDCS)", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "DEVICE", "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "National Institute of Neurological Disorders and Stroke (NINDS)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1273, "start_date": "2009-12-08", "completion_date": "2020-10-09", "has_results": false, "last_update_posted_date": "2026-09-18", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01019343" }, { "nct_id": "NCT02955043", "title": "Biobehavioral Intervention to Enhance Hematopoietic Stem Cell Transplant Recovery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hodgkin Lymphoma", "Non-Hodgkin Lymphoma", "Plasma Cell Myeloma", "Lymphoid Leukemia", "Myeloid Leukemia", "Myelodysplastic Syndromes", "Multiple Myeloma" ], "interventions": [ { "name": "Behavioral techniques", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "74 Years", "sex": "ALL", "summary": "18 Years to 74 Years" }, "enrollment_count": 39, "start_date": "2016-12-22", "completion_date": "2018-10-26", "has_results": false, "last_update_posted_date": "2019-11-15", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT02955043" }, { "nct_id": "NCT07224191", "title": "Hippocampal Oscillations During Exploration", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Epilepsy" ], "interventions": [ { "name": "Visual Exploration", "type": "OTHER" }, { "name": "Ambulatory Exploration", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 56, "start_date": "2026-02-25", "completion_date": "2028-10-08", "has_results": false, "last_update_posted_date": "2026-07-08", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07224191" }, { "nct_id": "NCT04063371", "title": "SAGE for the Early Detection of Cognitive Impairment at Primary Care Provider Visits", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cognitive Impairment" ], "interventions": [ { "name": "Self-Administered Gerocognitive Examination (SAGE) or Electronic Self-Administered Gerocognitive Examination (eSAGE)", "type": "OTHER" }, { "name": "Informant Conversation", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "65 Years to 89 Years" }, "enrollment_count": 300, "start_date": "2019-10-14", "completion_date": "2020-07-07", "has_results": true, "last_update_posted_date": "2024-05-14", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT04063371" }, { "nct_id": "NCT02968381", "title": "A Guided Imagery Tobacco Cessation Intervention Delivered by a Quit Line and Website", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tobacco Use", "Smoking Cessation", "Smoking, Tobacco", "Tobacco Smoking", "Guided Imagery" ], "interventions": [ { "name": "Imagery Intervention", "type": "BEHAVIORAL" }, { "name": "Control Condition", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Arizona", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 121, "start_date": "2018-05-01", "completion_date": "2022-01-21", "has_results": true, "last_update_posted_date": "2022-06-22", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "Tucson, Arizona", "locations": [ { "city": "Tucson", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT02968381" }, { "nct_id": "NCT04975139", "title": "Cognitive Changes of IDH-mutant and IDH-wildtype Glioma Patients After Chemoradiotherapy With Radiation Dose to the Resting State Networks", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Glioma" ], "interventions": [ { "name": "RS-fMRI", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 71, "start_date": "2020-09-02", "completion_date": "2033-10-31", "has_results": false, "last_update_posted_date": "2026-05-11", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04975139" }, { "nct_id": "NCT05159713", "title": "Study to Compare the Use of a Behavioral Health App Versus Care As Usual for 16-22 Year Olds with Depression", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression" ], "interventions": [ { "name": "dCBI", "type": "BEHAVIORAL" }, { "name": "Treatment as Usual", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "16 Years", "maximum_age": "22 Years", "sex": "ALL", "summary": "16 Years to 22 Years" }, "enrollment_count": 185, "start_date": "2022-06-01", "completion_date": "2024-08-30", "has_results": false, "last_update_posted_date": "2024-10-21", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 3, "location_summary": "San Diego, California • Boston, Massachusetts • Pittsburgh, Pennsylvania", "locations": [ { "city": "San Diego", "state": "California" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05159713" }, { "nct_id": "NCT04505371", "title": "Improving the Reach & Effectiveness of Smoking Cessation Services Targeted to Veterans Living With HIV", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infections", "Smoking", "Smoking Cessation" ], "interventions": [ { "name": "Wellness Intervention for Smokers with HIV", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Seattle Institute for Biomedical and Clinical Research", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 235, "start_date": "2021-06-04", "completion_date": "2026-03-31", "has_results": true, "last_update_posted_date": "2026-08-31", "last_synced_at": "2026-09-29T01:58:40.161Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT04505371" } ] }