{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=SIT&page=13", "query": { "intervention": "SIT", "page": 13 }, "page_size": 10 }, "pagination": { "page": 13, "page_size": 10, "total_count": 1197, "total_pages": 120, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=SIT&page=14&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=SIT&page=12&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-27T21:30:29.120Z", "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": "NCT01311206", "title": "Low Intensity Resistance Training With Partial Blood Flow Restriction for Quadriceps Strengthening", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Knee Osteoarthritis", "Symptomatic Knee Osteoarthritis" ], "interventions": [ { "name": "partial blood flow restriction", "type": "OTHER" }, { "name": "Low intensity exercise without partial blood flow restriction", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Iowa", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": "60 Years", "sex": "FEMALE", "summary": "45 Years to 60 Years · Female only" }, "enrollment_count": 50, "start_date": "2011-02", "completion_date": "2011-06", "has_results": false, "last_update_posted_date": "2011-06-28", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Iowa City, Iowa", "locations": [ { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT01311206" }, { "nct_id": "NCT07576413", "title": "Effects of Standing Desks and Intermittent Walking on Cognitive Fatigue", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sitting Position", "Overexertion From Maintaining Prolonged Standing Position", "Walking" ], "interventions": [ { "name": "Performance of cognitive tasks", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Clarkson University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 31, "start_date": "2018-06-01", "completion_date": "2018-12-15", "has_results": false, "last_update_posted_date": "2026-05-08", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Potsdam, New York", "locations": [ { "city": "Potsdam", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07576413" }, { "nct_id": "NCT02415660", "title": "Short-Term Response of Thoracic Spine Manipulation With or Without Trigger Point Dry Needling for Mechanical Neck Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Neck Pain" ], "interventions": [ { "name": "Thoracic spinal manipulation", "type": "PROCEDURE" }, { "name": "Trigger point dry needling", "type": "PROCEDURE" }, { "name": "Cervical range of motion exercises", "type": "BEHAVIORAL" }, { "name": "Posterior neck muscle activation exercise", "type": "BEHAVIORAL" }, { "name": "Trigger point dry needling sham", "type": "PROCEDURE" }, { "name": "Seirin J-type stainless steel needles, 0-2-0.3 x 40-50 mm", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "BEHAVIORAL", "DEVICE" ], "sponsor": "Brooke Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 42, "start_date": "2016-06-01", "completion_date": "2020-08-01", "has_results": false, "last_update_posted_date": "2021-02-02", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Fort Sam Houston, Texas", "locations": [ { "city": "Fort Sam Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02415660" }, { "nct_id": "NCT00000359", "title": "Treatments for Benign Paroxysmal Positional Vertigo (BPPV)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Vertigo" ], "interventions": [ { "name": "Canalith repositioning maneuver (Epley maneuver)", "type": "BEHAVIORAL" }, { "name": "Semont maneuver", "type": "BEHAVIORAL" }, { "name": "Brandt-Daroff exercises", "type": "BEHAVIORAL" }, { "name": "Vestibular habituation exercises", "type": "BEHAVIORAL" }, { "name": "ShamManeuver", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Baylor College of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 150, "start_date": "1998-10", "completion_date": "2003-06", "has_results": false, "last_update_posted_date": "2012-07-26", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00000359" }, { "nct_id": "NCT05534256", "title": "Reducing Sedentary Time in Patients With Cardiovascular Disease", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiovascular Diseases", "Heart Diseases", "Sedentary Behavior", "Physical Activity" ], "interventions": [ { "name": "Sit Less Program", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Vanderbilt University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 24, "start_date": "2022-09-13", "completion_date": "2024-07-30", "has_results": false, "last_update_posted_date": "2024-07-31", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT05534256" }, { "nct_id": "NCT01109602", "title": "Strength, Flexibility, And Balance Therapy After Stroke", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Stroke" ], "interventions": [ { "name": "Yoga focused on strength, flexibility, and balance", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 47, "start_date": "2010-07", "completion_date": "2011-09", "has_results": true, "last_update_posted_date": "2015-11-23", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT01109602" }, { "nct_id": "NCT06043063", "title": "Local Anesthesia Before Bulkamid Injection", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stress Urinary Incontinence", "Intrinsic Sphincter Deficiency" ], "interventions": [ { "name": "Topical lidocaine", "type": "PROCEDURE" }, { "name": "EMLA cream", "type": "PROCEDURE" }, { "name": "Periurethral block", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Medstar Health Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 23, "start_date": "2023-09-01", "completion_date": "2024-12-23", "has_results": false, "last_update_posted_date": "2025-05-16", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 3, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06043063" }, { "nct_id": "NCT06667193", "title": "Cold Water Exposure's Effects on Physical and Mental Health", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cold Exposure" ], "interventions": [ { "name": "Cold Water Immersion (CWI) - Cold Tub Immersion (CI)", "type": "OTHER" }, { "name": "Cold Water Immersion (CWI) - Cold Shower (CS)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Northern Colorado", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 36, "start_date": "2024-10-10", "completion_date": "2025-12-01", "has_results": false, "last_update_posted_date": "2026-09-30", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Greeley, Colorado", "locations": [ { "city": "Greeley", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT06667193" }, { "nct_id": "NCT03306992", "title": "Precision-exercise-prescription for Lung Cancer Patients Undergoing Surgery: The PEP Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Non Small Cell Lung Cancer", "Secondary Lung Cancer" ], "interventions": [ { "name": "Personalized Exercise Program", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 182, "start_date": "2017-11-07", "completion_date": "2022-05-31", "has_results": true, "last_update_posted_date": "2026-06-09", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT03306992" }, { "nct_id": "NCT07095036", "title": "Sensory Spinal Cord Stimulation", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain Management", "Pain, Intractable", "Pain, Chronic Disease" ], "interventions": [ { "name": "Spinal cord stimulation (SCS)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 10, "start_date": "2026-01-06", "completion_date": "2028-09-01", "has_results": false, "last_update_posted_date": "2026-02-04", "last_synced_at": "2026-10-27T21:30:29.120Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07095036" } ] }