{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Evaluation+%28behavior%29&page=39", "query": { "intervention": "Evaluation (behavior)", "page": 39 }, "page_size": 10 }, "pagination": { "page": 39, "page_size": 10, "total_count": 3642, "total_pages": 365, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Evaluation+%28behavior%29&page=40&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Evaluation+%28behavior%29&page=38&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-18T06:02:37.820Z", "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": "NCT05166694", "title": "Evaluating Personalized Therapeutics Clinic (PTC) on Drug-Drug Interactions and Drug-Gene Interactions", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Advanced Cancer", "Advanced Solid Tumor", "Mental Health Issue", "Behavior Disorders" ], "interventions": [ { "name": "Drug-Drug Interaction Profile", "type": "OTHER" }, { "name": "Drug-Gene Interaction Profile", "type": "OTHER" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1300, "start_date": "2022-11-30", "completion_date": "2027-11-01", "has_results": false, "last_update_posted_date": "2026-03-04", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05166694" }, { "nct_id": "NCT03690557", "title": "Examining Reach and Implementation of an Evidence-based Weight Loss Program in Rural Primary Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity" ], "interventions": [ { "name": "IncentaHealth", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Nebraska", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": null, "sex": "ALL", "summary": "19 Years and older" }, "enrollment_count": 98, "start_date": "2018-10-24", "completion_date": "2020-12-31", "has_results": false, "last_update_posted_date": "2023-09-28", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "David City, Nebraska", "locations": [ { "city": "David City", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT03690557" }, { "nct_id": "NCT04482036", "title": "The MObile AssessMENT of Behavioral and Psychological Symptoms of Dementia in Amnestic MCI and AD (MOMENT) Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alzheimer Disease", "Mild Memory Disturbance", "Mild Cognitive Impairment" ], "interventions": [ { "name": "Mobile Phone Application Assessments", "type": "OTHER" }, { "name": "Standard Assessments", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 20, "start_date": "2020-10-23", "completion_date": "2021-10-04", "has_results": true, "last_update_posted_date": "2023-09-01", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT04482036" }, { "nct_id": "NCT04649164", "title": "Learning to PERSEVERE: Peer Mentor Support and Caregiver Education in Lewy Body Dementia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lewy Body Disease", "Parkinson Disease Dementia", "Dementia With Lewy Bodies" ], "interventions": [ { "name": "Peer mentor support and caregiver intervention", "type": "BEHAVIORAL" }, { "name": "Focus group to provide feedback on educational materials and mentoring program", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Rush University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "21 Years to 90 Years" }, "enrollment_count": 87, "start_date": "2020-11-02", "completion_date": "2021-08-31", "has_results": true, "last_update_posted_date": "2023-01-25", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04649164" }, { "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": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04393909" }, { "nct_id": "NCT02426957", "title": "Brief Alcohol Intervention for Adolescents Who Have Attempted Suicide", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Suicide", "Alcohol Drinking" ], "interventions": [ { "name": "motivational enhancement therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Boston Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "13 Years to 17 Years" }, "enrollment_count": 50, "start_date": "2014-10", "completion_date": "2018-05", "has_results": false, "last_update_posted_date": "2018-07-24", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT02426957" }, { "nct_id": "NCT01532934", "title": "The Impact of Psychopathic Traits on the Efficacy of a Substance Use Intervention", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Substance Use", "Psychopathy" ], "interventions": [ { "name": "motivational enhancement therapy", "type": "BEHAVIORAL" }, { "name": "standard care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "University of Rochester", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 105, "start_date": "2009-08", "completion_date": "2014-07", "has_results": true, "last_update_posted_date": "2016-12-12", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Rochester, New York", "locations": [ { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01532934" }, { "nct_id": "NCT05113277", "title": "Development and Evaluation of a Tonic Immobility Focused Psychoeducational Intervention", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Posttraumatic Stress Disorder", "Tonic Immobility Response" ], "interventions": [ { "name": "Tonic Immobility Psychoeducation (TIP)", "type": "BEHAVIORAL" }, { "name": "Health Education Training (HET)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Florida State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 51, "start_date": "2021-09-27", "completion_date": "2022-05-31", "has_results": true, "last_update_posted_date": "2024-08-23", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Tallahassee, Florida", "locations": [ { "city": "Tallahassee", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05113277" }, { "nct_id": "NCT07240792", "title": "Development of a College Student-Delivered Cognitive-Behavioral Therapy (CBT) Intervention for Rural High School Students", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Anxiety", "Stress" ], "interventions": [ { "name": "Student Delivered Cognitive Behavioral Therapy Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Milton S. Hershey Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "13 Years to 18 Years" }, "enrollment_count": 40, "start_date": "2026-02-25", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2026-04-15", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Hershey, Pennsylvania", "locations": [ { "city": "Hershey", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07240792" }, { "nct_id": "NCT00343434", "title": "Soy-Based Meal Replacement in Helping Women With Stage I, Stage II, or Stage III Breast Cancer in Complete Remission Lose Weight", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Obesity" ], "interventions": [ { "name": "behavioral dietary intervention", "type": "BEHAVIORAL" }, { "name": "exercise intervention", "type": "BEHAVIORAL" }, { "name": "soy isoflavones", "type": "DIETARY_SUPPLEMENT" }, { "name": "soy protein isolate", "type": "DIETARY_SUPPLEMENT" }, { "name": "counseling intervention", "type": "OTHER" }, { "name": "educational intervention", "type": "OTHER" }, { "name": "psychosocial assessment and care", "type": "PROCEDURE" }, { "name": "quality-of-life assessment", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "DIETARY_SUPPLEMENT", "OTHER", "PROCEDURE" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "21 Years to 120 Years" }, "enrollment_count": 25, "start_date": "2005-01", "completion_date": null, "has_results": false, "last_update_posted_date": "2017-01-19", "last_synced_at": "2026-10-18T06:02:37.820Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00343434" } ] }