{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Vibration+perception", "query": { "intervention": "Vibration perception" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 48, "total_pages": 5, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Vibration+perception&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-06T17:37:48.353Z", "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": "2025-09-17", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07071350" }, { "nct_id": "NCT05058846", "title": "Pilot Study of Pancreatic Cancer Screening", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Pancreatic Carcinoma" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Cholangiopancreatography", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Endoscopic ultrasound", "type": "PROCEDURE" }, { "name": "Questionnaires", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2022-01-20", "completion_date": "2032-01-31", "has_results": false, "last_update_posted_date": "2026-08-11", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05058846" }, { "nct_id": "NCT06934356", "title": "Subcortical Arousal in Perceptual Awareness", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Epilepsy" ], "interventions": [ { "name": "EEG", "type": "DEVICE" }, { "name": "Eye Tracking", "type": "DEVICE" }, { "name": "Behavioral task", "type": "DEVICE" }, { "name": "fMRI", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DEVICE", "DIAGNOSTIC_TEST" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": null, "sex": "ALL", "summary": "13 Years and older" }, "enrollment_count": 202, "start_date": "2025-10-13", "completion_date": "2030-12", "has_results": false, "last_update_posted_date": "2026-08-10", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 8, "location_summary": "New Haven, Connecticut • Kansas City, Kansas • Boston, Massachusetts + 5 more", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Kansas City", "state": "Kansas" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Rochester", "state": "Minnesota" }, { "city": "Lebanon", "state": "New Hampshire" } ], "official_url": "https://clinicaltrials.gov/study/NCT06934356" }, { "nct_id": "NCT02062840", "title": "The Brain on Whole Body Hyperthermia: A Neuroimaging Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Major Depression" ], "interventions": [ { "name": "High intensity whole-body infrared heating", "type": "DEVICE" }, { "name": "Low intensity whole-body infrared heating", "type": "DEVICE" }, { "name": "Functional Magnetic Resonance Imaging (fMRI) and electrocardiogram (EKG)", "type": "DEVICE" }, { "name": "Questionnaires", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of Arizona", "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": 23, "start_date": "2014-02", "completion_date": "2015-05", "has_results": false, "last_update_posted_date": "2015-08-10", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "Tucson, Arizona", "locations": [ { "city": "Tucson", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT02062840" }, { "nct_id": "NCT07553273", "title": "Vibratory Anesthesia on Pain Following Corticosteroid Injections", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bilateral Arthritis of Wrist", "Tendinopathy", "Arthropathy", "Compression Neuropathy", "Bilateral Arthritis of Hands" ], "interventions": [ { "name": "Digivibe Device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The University of Texas Medical Branch, Galveston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 165, "start_date": "2026-01-14", "completion_date": "2027-04", "has_results": false, "last_update_posted_date": "2026-07-10", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "Galveston, Texas", "locations": [ { "city": "Galveston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07553273" }, { "nct_id": "NCT02962154", "title": "Neurocardiac Interactions Evaluated by Anatomic and Physiologic MRI Assessment", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ischemia", "Stress, Mental" ], "interventions": [ { "name": "Coronary CT Angiography", "type": "RADIATION" }, { "name": "Mood Symptom Scale", "type": "OTHER" }, { "name": "Anxiety Symptom Scale", "type": "OTHER" }, { "name": "Chronic Stress Inventories", "type": "OTHER" }, { "name": "Psychosocial Function Questionnaires", "type": "OTHER" }, { "name": "General Health and quality of life questionnaires", "type": "OTHER" }, { "name": "Magnetic Resonance Imaging", "type": "OTHER" } ], "intervention_types": [ "RADIATION", "OTHER" ], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 0, "start_date": "2016-02", "completion_date": "2018-01", "has_results": false, "last_update_posted_date": "2018-01-09", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02962154" }, { "nct_id": "NCT04802005", "title": "Effects of a Short-term Aerobic Interval Exercise Program on Cardiac Fat and Function in Women With Obesity: A Pilot Study", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity" ], "interventions": [ { "name": "Aerobic Interval Training", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Southern Illinois University Edwardsville", "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": 0, "start_date": "2021-03-16", "completion_date": "2021-04-16", "has_results": false, "last_update_posted_date": "2021-09-21", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "Edwardsville, Illinois", "locations": [ { "city": "Edwardsville", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04802005" }, { "nct_id": "NCT02394704", "title": "Intervention for Intrusive Negative Thinking", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Intrusive Negative Thinking" ], "interventions": [ { "name": "Sensory attention training", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Pittsburgh", "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": 194, "start_date": "2015-11-01", "completion_date": "2021-08-17", "has_results": false, "last_update_posted_date": "2021-12-07", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02394704" }, { "nct_id": "NCT04381182", "title": "Heart Rate Variability and Stress Management Enhancement", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stress", "Heart Rate Variability" ], "interventions": [ { "name": "Apollo Wearable Device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Joseph Maroon", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 20, "start_date": "2021-09-01", "completion_date": "2022-08-20", "has_results": false, "last_update_posted_date": "2022-12-06", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04381182" }, { "nct_id": "NCT06961864", "title": "Investigating Brain Function in People With and Without Visual Snow Syndrome Using Adaptation to Visual Stimuli", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Visual Snow Syndrome", "Migraine", "Healthy" ], "interventions": [ { "name": "Visual Adaptation", "type": "BEHAVIORAL" }, { "name": "Assessments and Questionnaires", "type": "BEHAVIORAL" }, { "name": "Functional Magnetic Resonance Imaging (fMRI)", "type": "DEVICE" }, { "name": "Magnetic Resonance Imaging (MRS)", "type": "DEVICE" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 100, "start_date": "2025-04-11", "completion_date": "2030-03-31", "has_results": false, "last_update_posted_date": "2026-01-14", "last_synced_at": "2026-09-06T17:37:48.353Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06961864" } ] }