{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Physical+exam&page=2", "query": { "intervention": "Physical exam", "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=Physical+exam&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-26T02:37:26.664Z", "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": "NCT00762125", "title": "Subgroups of Fibromyalgia Syndrome (FMS): Symptoms, Beliefs, and Tailored Treatment", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Fibromyalgia" ], "interventions": [ { "name": "CR+ST", "type": "BEHAVIORAL" }, { "name": "ET", "type": "BEHAVIORAL" }, { "name": "AC treatment", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 266, "start_date": "2005-12", "completion_date": "2012-01", "has_results": false, "last_update_posted_date": "2014-12-02", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT00762125" }, { "nct_id": "NCT04093440", "title": "Cardiometabolic Syndrome Response to Therapeutic Lifestyle Changes", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Metabolic Syndrome", "ASCVD", "Lifestyle Risk Reduction" ], "interventions": [ { "name": "lifestyle modification", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Holy Cross Hospital, Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 250, "start_date": "2019-10", "completion_date": "2021-12", "has_results": false, "last_update_posted_date": "2019-09-18", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Fort Lauderdale, Florida", "locations": [ { "city": "Fort Lauderdale", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04093440" }, { "nct_id": "NCT03490240", "title": "Project BIPAMS: Behavioral Intervention for Physical Activity in Multiple Sclerosis", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Multiple Sclerosis" ], "interventions": [ { "name": "BIPAMS", "type": "BEHAVIORAL" }, { "name": "WELLMS", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 280, "start_date": "2018-03-01", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2025-12-22", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT03490240" }, { "nct_id": "NCT03412916", "title": "Integrating Mind-Body Skills With Physical Activity to Improve Physical and Emotional Outcomes in Patients With Chronic Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain", "Chronic Pain", "Physical Activity" ], "interventions": [ { "name": "GetActive", "type": "BEHAVIORAL" }, { "name": "Get Active with Fitbit", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 82, "start_date": "2017-10-01", "completion_date": "2020-06-30", "has_results": true, "last_update_posted_date": "2025-10-14", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03412916" }, { "nct_id": "NCT06953648", "title": "Remotely Monitored, Mobile Health-supported, High Intensity Interval Training Before Hematopoietic Stem Cell Transplant", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hematopoietic Stem Cell Transplantation", "Cardiorespiratory Fitness" ], "interventions": [ { "name": "High Intensity Interval Training", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Kansas Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 126, "start_date": "2025-05", "completion_date": "2030-03", "has_results": false, "last_update_posted_date": "2025-05-01", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 3, "location_summary": "Kansas City, Kansas • Durham, North Carolina • Houston, Texas", "locations": [ { "city": "Kansas City", "state": "Kansas" }, { "city": "Durham", "state": "North Carolina" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06953648" }, { "nct_id": "NCT02143414", "title": "Blinatumomab and Combination Chemotherapy or Dasatinib, Prednisone, and Blinatumomab in Treating Older Patients With Acute Lymphoblastic Leukemia", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Acute Lymphoblastic Leukemia", "B Acute Lymphoblastic Leukemia", "B Acute Lymphoblastic Leukemia With t(9;22)(q34.1;q11.2); BCR-ABL1", "Recurrent Acute Lymphoblastic Leukemia", "Refractory Acute Lymphoblastic Leukemia" ], "interventions": [ { "name": "Biopsy Procedure", "type": "PROCEDURE" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Blinatumomab", "type": "BIOLOGICAL" }, { "name": "Bone Marrow Aspiration and Biopsy", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Dasatinib", "type": "DRUG" }, { "name": "Echocardiography Test", "type": "PROCEDURE" }, { "name": "Lumbar Puncture", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Mercaptopurine", "type": "DRUG" }, { "name": "Methotrexate", "type": "DRUG" }, { "name": "Methotrexate Sodium", "type": "DRUG" }, { "name": "Prednisone", "type": "DRUG" }, { "name": "Vincristine", "type": "DRUG" }, { "name": "Vincristine Sulfate", "type": "DRUG" }, { "name": "X-Ray Imaging", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "BIOLOGICAL", "DRUG" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 53, "start_date": "2015-06-30", "completion_date": "2027-06-06", "has_results": true, "last_update_posted_date": "2026-08-04", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 195, "location_summary": "Birmingham, Alabama • Tucson, Arizona • Little Rock, Arkansas + 139 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Duarte", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02143414" }, { "nct_id": "NCT03303404", "title": "24-hour Blood Pressure Measurements and Ischemic Conditioning", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Blood Pressure" ], "interventions": [ { "name": "Ambulatory (24-hour) Blood Pressure", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "30 Years to 60 Years" }, "enrollment_count": 22, "start_date": "2017-09-12", "completion_date": "2018-09-20", "has_results": true, "last_update_posted_date": "2020-12-22", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03303404" }, { "nct_id": "NCT06971978", "title": "Study to Assess the Effectiveness of a Heat Risk Reduction Decision Support Platform and the Barriers and Facilitators of Its Implementation With 30 US Local Health Department Sites", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Extreme Heat", "Heat Health", "Extreme Heat Waves", "Heat", "Emergency Preparedness", "Disaster Management", "Disaster Planning", "Disasters" ], "interventions": [ { "name": "Online decision support platform to support evidence-based heat health risk assessment and extreme heat event preparedness planning", "type": "OTHER" }, { "name": "Heat and health risk assessment and preparedness information", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2025-08-01", "completion_date": "2027-08-31", "has_results": false, "last_update_posted_date": "2026-06-11", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06971978" }, { "nct_id": "NCT00042185", "title": "Eating Disorder Prevention Programs", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Eating Disorders" ], "interventions": [ { "name": "Dissonance Eating Disorder Prevention Program", "type": "BEHAVIORAL" }, { "name": "Healthy Weight Intervention", "type": "BEHAVIORAL" }, { "name": "Expressive Writing Control Condition", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": "19 Years", "sex": "FEMALE", "summary": "14 Years to 19 Years · Female only" }, "enrollment_count": 450, "start_date": "2001-02", "completion_date": "2007-05", "has_results": false, "last_update_posted_date": "2013-09-27", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00042185" }, { "nct_id": "NCT00499785", "title": "Physical and Mental Assessment of Older Patients With Newly Diagnosed Acute Myeloid Leukemia", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cognitive/Functional Effects", "Depression", "Leukemia" ], "interventions": [], "intervention_types": [], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "60 Years to 120 Years" }, "enrollment_count": 11, "start_date": "2007-06", "completion_date": "2012-01", "has_results": false, "last_update_posted_date": "2017-05-30", "last_synced_at": "2026-09-26T02:37:26.664Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00499785" } ] }