{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Exercise-based+behavioral+therapy&page=7", "query": { "intervention": "Exercise-based behavioral therapy", "page": 7 }, "page_size": 10 }, "pagination": { "page": 7, "page_size": 10, "total_count": 951, "total_pages": 96, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Exercise-based+behavioral+therapy&page=8&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Exercise-based+behavioral+therapy&page=6&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-26T12:48:06.614Z", "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": "NCT02613364", "title": "Yoga, Survivorship Health Education, and Cognitive Behavioral Therapy in Reducing Insomnia in Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer Survivor", "Insomnia", "Malignant Neoplasm" ], "interventions": [ { "name": "Behavioral Intervention", "type": "BEHAVIORAL" }, { "name": "Cognitive Intervention", "type": "OTHER" }, { "name": "Educational Intervention", "type": "OTHER" }, { "name": "Laboratory Biomarker Analysis", "type": "OTHER" }, { "name": "Monitoring Device", "type": "DEVICE" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "DEVICE" ], "sponsor": "University of Rochester NCORP Research Base", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 746, "start_date": "2016-08-31", "completion_date": "2020-02-04", "has_results": true, "last_update_posted_date": "2024-05-01", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 16, "location_summary": "Honolulu, Hawaii • Decatur, Illinois • Wichita, Kansas + 13 more", "locations": [ { "city": "Honolulu", "state": "Hawaii" }, { "city": "Decatur", "state": "Illinois" }, { "city": "Wichita", "state": "Kansas" }, { "city": "New Orleans", "state": "Louisiana" }, { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT02613364" }, { "nct_id": "NCT00283816", "title": "Impact of Metformin in Teens With Polycystic Ovary Syndrome (PCOS) on Oral Contraceptive Therapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Polycystic Ovary Syndrome" ], "interventions": [ { "name": "Metformin", "type": "DRUG" }, { "name": "Oral Contraceptive Pill", "type": "DRUG" }, { "name": "Lifestyle Management Program", "type": "BEHAVIORAL" }, { "name": "Quality of Life Questionnaire", "type": "BEHAVIORAL" }, { "name": "Oral Glucose Tolerance Test", "type": "PROCEDURE" }, { "name": "Blood work", "type": "PROCEDURE" }, { "name": "Abdominal Ultra Sound", "type": "PROCEDURE" }, { "name": "Dual-energy x-ray absorptiometry (DEXA scan)", "type": "PROCEDURE" }, { "name": "placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG", "BEHAVIORAL", "PROCEDURE" ], "sponsor": "University of Rochester", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "18 Years", "sex": "FEMALE", "summary": "12 Years to 18 Years · Female only" }, "enrollment_count": 36, "start_date": "2006-01", "completion_date": "2008-01", "has_results": true, "last_update_posted_date": "2015-05-15", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "Rochester, New York", "locations": [ { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00283816" }, { "nct_id": "NCT04737915", "title": "Virtual Reality Exposure Versus In Vivo Exposure for Fear of Heights", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Fear of Heights", "Acrophobia", "Specific Phobia", "Anxiety Disorder" ], "interventions": [ { "name": "Exposure Therapy (In Vivo)", "type": "BEHAVIORAL" }, { "name": "Exposure Therapy (Virtual Reality)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Notre Dame", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 114, "start_date": "2018-06-11", "completion_date": "2019-03-06", "has_results": false, "last_update_posted_date": "2021-02-08", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "Notre Dame, Indiana", "locations": [ { "city": "Notre Dame", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT04737915" }, { "nct_id": "NCT05849064", "title": "Concussion Treatment in Older Adults", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Concussion, Mild" ], "interventions": [ { "name": "Behavioral Control", "type": "BEHAVIORAL" }, { "name": "Targeted Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "50 Years to 99 Years" }, "enrollment_count": 56, "start_date": "2023-09-07", "completion_date": "2026-06-15", "has_results": false, "last_update_posted_date": "2026-08-06", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05849064" }, { "nct_id": "NCT06044571", "title": "Optimizing Telehealth-delivery of a Weight Loss Intervention in Older Adults", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity", "Multiple Chronic Conditions" ], "interventions": [ { "name": "Prescriptive", "type": "OTHER" }, { "name": "Behavioral", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "65 Years to 85 Years" }, "enrollment_count": 180, "start_date": "2024-04-16", "completion_date": "2027-09-01", "has_results": false, "last_update_posted_date": "2026-02-06", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06044571" }, { "nct_id": "NCT01566864", "title": "Multi-Method Health System Quality Improvement Intervention to Reduce Hypertension Disparities", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension" ], "interventions": [ { "name": "Improve clinic based measurement of blood pressure", "type": "BEHAVIORAL" }, { "name": "Provider education system to promote patient-centered care", "type": "BEHAVIORAL" }, { "name": "Introduce care management system in clinics", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 66570, "start_date": "2011-04", "completion_date": "2015-04", "has_results": false, "last_update_posted_date": "2018-01-05", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01566864" }, { "nct_id": "NCT04393909", "title": "Improving Safety of Diagnosis and Therapy in the Inpatient Setting", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Delirium", "Confusion", "Mental Status Change", "Back Pain", "Hip Pain Chronic", "Chest Pain", "Asthma", "COPD", "Cellulitis", "Soft Tissue Infections", "Cough", "Deep Vein Thrombosis", "Pulmonary Embolism", "Venous Thromboembolism", "Dyspnea", "Electrolyte Metabolism Abnormal", "Fever", "Failure to Thrive", "Weakness", "Protein-Calorie Malnutrition", "Headache", "Neck Pain", "Hypoxia", "Pneumonia", "Sepsis", "Syncope", "Vomiting", "Diarrhea", "Leg Pain", "Abdominal Pain" ], "interventions": [ { "name": "Diagnostic Uncertainty Educational Curriculum", "type": "BEHAVIORAL" }, { "name": "Diagnostic Timeout", "type": "BEHAVIORAL" }, { "name": "Patient Diagnostic (Dx) Questionnaire", "type": "BEHAVIORAL" }, { "name": "Enhancements to Epic-integrated Quality & Safety Dashboard", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Brigham and Women's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 700, "start_date": "2019-07-01", "completion_date": "2021-12-30", "has_results": false, "last_update_posted_date": "2022-07-26", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04393909" }, { "nct_id": "NCT01339806", "title": "The Study of Cognitive Rehabilitation Effectiveness for Mild Traumatic Brain Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Traumatic Brain Injury With Brief Loss of Consciousness", "Traumatic Brain Injury With No Loss of Consciousness" ], "interventions": [ { "name": "Cognitive Rehab", "type": "BEHAVIORAL" }, { "name": "Brainworks", "type": "BEHAVIORAL" }, { "name": "Informational Handout/Provider Visits", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Brooke Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 143, "start_date": "2011-06", "completion_date": "2014-08", "has_results": false, "last_update_posted_date": "2015-02-09", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01339806" }, { "nct_id": "NCT03527641", "title": "United for Health: Type 2 Diabetes Prevention in Latino Teens", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prediabetic State", "Insulin Resistance", "Type2 Diabetes", "Stress", "Adolescent Development", "Family Research" ], "interventions": [ { "name": "CookingMatters", "type": "BEHAVIORAL" }, { "name": "Parent Education", "type": "BEHAVIORAL" }, { "name": "Physical Activity", "type": "BEHAVIORAL" }, { "name": "Health Education", "type": "BEHAVIORAL" }, { "name": "Mindfulness-based Stress Reduction", "type": "BEHAVIORAL" }, { "name": "Brief Mindfulness Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Colorado State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": "15 Years", "sex": "ALL", "summary": "12 Years to 15 Years" }, "enrollment_count": 20, "start_date": "2018-05-01", "completion_date": "2019-04-30", "has_results": false, "last_update_posted_date": "2019-08-26", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 2, "location_summary": "Fort Collins, Colorado", "locations": [ { "city": "Fort Collins", "state": "Colorado" }, { "city": "Fort Collins", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT03527641" }, { "nct_id": "NCT07187024", "title": "Efficacy of an Evidence-based Telehealth Intervention in Modifying Health Behavior", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-traumatic Osteoarthritis", "Knee Sprain", "Knee Injuries" ], "interventions": [ { "name": "mCare PTOA Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Keller Army Community Hospital", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "54 Years", "sex": "ALL", "summary": "18 Years to 54 Years" }, "enrollment_count": 65, "start_date": "2020-07-24", "completion_date": "2027-09-01", "has_results": false, "last_update_posted_date": "2026-09-30", "last_synced_at": "2026-10-26T12:48:06.614Z", "location_count": 1, "location_summary": "West Point, New York", "locations": [ { "city": "West Point", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07187024" } ] }