{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Tampa+Scale+of+Kinesiophobia", "query": { "intervention": "Tampa Scale of Kinesiophobia" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 5, "total_pages": 1, "next_page_url": null, "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-10-02T15:23:23.390Z", "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": "NCT05461092", "title": "Regional Nerve Blocks to Improve Analgesia and Recovery in Older Adults Undergoing Spinal Fusion", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Delirium", "Pain, Back", "Spinal Fusion", "Thoracolumbar Interfascial Plane Block" ], "interventions": [ { "name": "Thoracolumbar Interfascial Plane (TLIP) Block of bupivacaine", "type": "DRUG" }, { "name": "Blood Test", "type": "DIAGNOSTIC_TEST" }, { "name": "3D CAM Delirium Severity Scoring", "type": "OTHER" }, { "name": "Generalized Anxiety Disorder 7-item (GAD-7) scale", "type": "OTHER" }, { "name": "Numerical Rating Score (NRS)", "type": "OTHER" }, { "name": "PROMIS-Pain Interference", "type": "OTHER" }, { "name": "Oswestry Disability Index (ODI)", "type": "OTHER" }, { "name": "Saint Louis University Mental Status Examination (SLUMs)", "type": "OTHER" }, { "name": "Delirium Rating Scale-Revised-98 (DRS)", "type": "OTHER" }, { "name": "Telephone Interview for Cognitive Status - Modified (TICS-M)", "type": "OTHER" }, { "name": "Opioid Equivalents measured by Morphine Milligram Equivalents (MME)", "type": "OTHER" }, { "name": "Patient Health Questionnaire depression scale (PHQ-8)", "type": "OTHER" }, { "name": "Pain Catastrophizing", "type": "OTHER" }, { "name": "Fear Avoidance Beliefs Questionnaire (FABQ)", "type": "OTHER" }, { "name": "Opioid Side Effects and Likeability Questionnaire", "type": "OTHER" }, { "name": "Daily Pain Trajectory", "type": "OTHER" }, { "name": "Tampa Scale of Kinesiophobia", "type": "OTHER" }, { "name": "Quality of Recovery 15", "type": "OTHER" } ], "intervention_types": [ "DRUG", "DIAGNOSTIC_TEST", "OTHER" ], "sponsor": "University of Iowa", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 50, "start_date": "2024-01-01", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-03-27", "last_synced_at": "2026-10-02T15:23:23.390Z", "location_count": 1, "location_summary": "Iowa City, Iowa", "locations": [ { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT05461092" }, { "nct_id": "NCT05122728", "title": "Post-Concussion Musculoskeletal Injury Risks", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Musculoskeletal Injury" ], "interventions": [ { "name": "Post-Concussion Neuromuscular Function and Musculoskeletal Injury Risk Assessment", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Walter Reed National Military Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 148, "start_date": "2022-10-20", "completion_date": "2027-09-30", "has_results": false, "last_update_posted_date": "2026-01-27", "last_synced_at": "2026-10-02T15:23:23.390Z", "location_count": 3, "location_summary": "Athens, Georgia • Bethesda, Maryland • Fort Bragg, North Carolina", "locations": [ { "city": "Athens", "state": "Georgia" }, { "city": "Bethesda", "state": "Maryland" }, { "city": "Fort Bragg", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05122728" }, { "nct_id": "NCT06442306", "title": "Evaluation of Pain Neuroscience Education for Patients Who Experience Chronic Pain With Concurrent Opioid Dependence", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Pain", "Opioid Dependence" ], "interventions": [ { "name": "Pain Neuroscience Education", "type": "OTHER" }, { "name": "General Health Education", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Wichita State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "95 Years", "sex": "ALL", "summary": "18 Years to 95 Years" }, "enrollment_count": 21, "start_date": "2020-01-03", "completion_date": "2021-01-15", "has_results": false, "last_update_posted_date": "2024-06-04", "last_synced_at": "2026-10-02T15:23:23.390Z", "location_count": 1, "location_summary": "Lexington, Kentucky", "locations": [ { "city": "Lexington", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT06442306" }, { "nct_id": "NCT05976269", "title": "Bilateral Knee Pain and Dry Needling", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Patellofemoral Pain" ], "interventions": [ { "name": "Dry needling", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 60, "start_date": "2020-07-21", "completion_date": "2030-07-21", "has_results": false, "last_update_posted_date": "2026-02-25", "last_synced_at": "2026-10-02T15:23:23.390Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05976269" }, { "nct_id": "NCT05111925", "title": "Pre- and Post-neuromusculoskeletal Injury Risk Evaluation for Return-to-Duty Enhancement", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Musculoskeletal Injuries" ], "interventions": [ { "name": "PREPARE Initial Clinical Assessment - Pilot (two iterations)", "type": "OTHER" }, { "name": "PREPARE Initial Clinical Assessment - Pre-Injury (one iteration)", "type": "OTHER" }, { "name": "PREPARE Initial Clinical Assessment - Post-Injury (up to three iterations)", "type": "OTHER" }, { "name": "PREPARE Optimized Clinical Assessment", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Womack Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "44 Years", "sex": "ALL", "summary": "18 Years to 44 Years" }, "enrollment_count": 2690, "start_date": "2022-10-26", "completion_date": "2028-05-31", "has_results": false, "last_update_posted_date": "2026-06-03", "last_synced_at": "2026-10-02T15:23:23.390Z", "location_count": 2, "location_summary": "Bethesda, Maryland • Fort Liberty, North Carolina", "locations": [ { "city": "Bethesda", "state": "Maryland" }, { "city": "Fort Liberty", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05111925" } ] }