{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=6+Week+Intervention&page=38", "query": { "intervention": "6 Week Intervention", "page": 38 }, "page_size": 10 }, "pagination": { "page": 38, "page_size": 10, "total_count": 4678, "total_pages": 468, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=6+Week+Intervention&page=39&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=6+Week+Intervention&page=37&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-07T12:07:42.001Z", "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": "NCT02831114", "title": "Evaluating the Effects of Acupuncture in the Treatment of Taxane Induces Peripheral Neuropathy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Peripheral Neuropathy" ], "interventions": [ { "name": "Acupuncture", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Prisma Health-Upstate", "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": 18, "start_date": "2016-05", "completion_date": "2018-01", "has_results": false, "last_update_posted_date": "2018-01-04", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 1, "location_summary": "Greenville, South Carolina", "locations": [ { "city": "Greenville", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02831114" }, { "nct_id": "NCT07547878", "title": "Rapid and Simultaneous Initiation of Four Guideline-Directed CKD Therapies (RAPID-CKD)", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Chronic Kidney Disease", "Type 2 Diabetes" ], "interventions": [ { "name": "Finerenone", "type": "DRUG" }, { "name": "Semaglutide", "type": "DRUG" }, { "name": "Lotensin", "type": "DRUG" }, { "name": "Capoten", "type": "DRUG" }, { "name": "Enalapril", "type": "DRUG" }, { "name": "Monopril", "type": "DRUG" }, { "name": "Lisinopril", "type": "DRUG" }, { "name": "Univasc", "type": "DRUG" }, { "name": "Aceon", "type": "DRUG" }, { "name": "Accupril", "type": "DRUG" }, { "name": "Altace", "type": "DRUG" }, { "name": "Mavik", "type": "DRUG" }, { "name": "Edarbi", "type": "DRUG" }, { "name": "Atacand", "type": "DRUG" }, { "name": "Avapro", "type": "DRUG" }, { "name": "Cozaar", "type": "DRUG" }, { "name": "Benicar", "type": "DRUG" }, { "name": "Micardis", "type": "DRUG" }, { "name": "Diovan", "type": "DRUG" }, { "name": "Invokana", "type": "DRUG" }, { "name": "Farxiga", "type": "DRUG" }, { "name": "Jardiance", "type": "DRUG" }, { "name": "Ertugliflozin", "type": "DRUG" }, { "name": "Brenzavvy", "type": "DRUG" }, { "name": "Sotagliflozin", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Baylor Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "84 Years", "sex": "ALL", "summary": "18 Years to 84 Years" }, "enrollment_count": 64, "start_date": "2026-04-08", "completion_date": "2029-03-31", "has_results": false, "last_update_posted_date": "2026-10-13", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 1, "location_summary": "Temple, Texas", "locations": [ { "city": "Temple", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07547878" }, { "nct_id": "NCT03819478", "title": "Utilizing Protein During Weight Loss to Impact Physical Function and Bone", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity", "Weight Loss", "Diet Modification", "Aging", "Weight Change, Body", "Dietary Habits", "Osteopenia, Osteoporosis", "Bone Loss", "Fractures, Bone" ], "interventions": [ { "name": "Weight loss intervention months 0-6", "type": "BEHAVIORAL" }, { "name": "Exercise intervention months 0-6", "type": "BEHAVIORAL" }, { "name": "NutraBio™ CarboMax Supplement", "type": "DIETARY_SUPPLEMENT" }, { "name": "6-month NutraBio™ 100% Whey Protein Isolate Supplement", "type": "DIETARY_SUPPLEMENT" }, { "name": "18-month NutraBio™ 100% Whey Protein Isolate Supplement", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "BEHAVIORAL", "DIETARY_SUPPLEMENT" ], "sponsor": "Wake Forest University Health Sciences", "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": 187, "start_date": "2017-05-03", "completion_date": "2022-04-28", "has_results": true, "last_update_posted_date": "2024-01-19", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03819478" }, { "nct_id": "NCT07228143", "title": "Stepped Care Treatment for Anxiety Resilience", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Generalized Anxiety Disorder (GAD)", "Social Anxiety Disorder (SAD)", "Separation Anxiety Disorder", "Specific Phobia", "Obsessive Compulsive Disorder (OCD)", "Panic Disorder (With or Without Agoraphobia)" ], "interventions": [ { "name": "Relaxation and Mentorship Training (RMT)", "type": "BEHAVIORAL" }, { "name": "Stepped Care Targeting Exposure and Parenting for Anxiety (STEP-A)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Andrew Wiese", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "7 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "7 Years to 17 Years" }, "enrollment_count": 106, "start_date": "2026-01-05", "completion_date": "2028-04-30", "has_results": false, "last_update_posted_date": "2026-03-02", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07228143" }, { "nct_id": "NCT07396935", "title": "Increasing Treatment Access in Trauma Exposed Children: Developing an Adapted Step One Intervention (Pilot)", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Trauma", "Posttraumatic Stress Disorder" ], "interventions": [ { "name": "Personalized Stepped Care Cognitive Behavioral Therapy for Children after Trauma (pSC-CBT-CT)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "7 Years", "maximum_age": "14 Years", "sex": "ALL", "summary": "7 Years to 14 Years" }, "enrollment_count": 7, "start_date": "2026-04-01", "completion_date": "2026-08-31", "has_results": false, "last_update_posted_date": "2026-02-09", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07396935" }, { "nct_id": "NCT06205225", "title": "iCardia4HF: Multi-component mHealth Intervention for Patients With Heart Failure", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Heart Failure" ], "interventions": [ { "name": "Text4HF", "type": "BEHAVIORAL" }, { "name": "MyApps", "type": "BEHAVIORAL" }, { "name": "MyApps & Text4HF", "type": "BEHAVIORAL" }, { "name": "Enhanced Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Illinois Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 360, "start_date": "2024-10-04", "completion_date": "2028-09-30", "has_results": false, "last_update_posted_date": "2026-01-30", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 2, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06205225" }, { "nct_id": "NCT03635164", "title": "Radiotherapy With Durvalumab Prior to Surgical Resection for HPV Negative Squamous Cell Carcinoma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Squamous Cell Carcinoma of the Head and Neck" ], "interventions": [ { "name": "Durvalumab", "type": "DRUG" }, { "name": "Stereotactic Body Radiation Therapy (SBRT)", "type": "RADIATION" }, { "name": "Standard of Care Therapy", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "RADIATION", "PROCEDURE" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 21, "start_date": "2018-11-12", "completion_date": "2023-05-02", "has_results": false, "last_update_posted_date": "2025-06-27", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 3, "location_summary": "Aurora, Colorado • Colorado Springs, Colorado • Fort Collins, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Colorado Springs", "state": "Colorado" }, { "city": "Fort Collins", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT03635164" }, { "nct_id": "NCT04162847", "title": "Harnessing Mobile Technology to Reduce Mental Health Disorders in College Populations", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anxiety Disorders", "Depressive Disorder", "Eating Disorders" ], "interventions": [ { "name": "SilverCloud Health Intervention", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6205, "start_date": "2019-10-07", "completion_date": "2023-12-31", "has_results": true, "last_update_posted_date": "2025-04-23", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 4, "location_summary": "Palo Alto, California • Ann Arbor, Michigan • St Louis, Missouri + 1 more", "locations": [ { "city": "Palo Alto", "state": "California" }, { "city": "Ann Arbor", "state": "Michigan" }, { "city": "St Louis", "state": "Missouri" }, { "city": "State College", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04162847" }, { "nct_id": "NCT04727047", "title": "NMES for Achilles Tendon Rupture", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Achilles Tendon Rupture" ], "interventions": [ { "name": "neuromuscular electrical stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Penn State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 8, "start_date": "2023-02-15", "completion_date": "2024-12-31", "has_results": true, "last_update_posted_date": "2026-09-22", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 1, "location_summary": "State College, Pennsylvania", "locations": [ { "city": "State College", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04727047" }, { "nct_id": "NCT07038317", "title": "A Text Messaging Trial to Test Vaping Health Messages Optimized to Young Adults' Vaping Status", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vaping Behaviors", "Message Exposure", "Young Adults" ], "interventions": [ { "name": "Intervention", "type": "OTHER" }, { "name": "Control", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Hawaii", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "24 Years", "sex": "ALL", "summary": "18 Years to 24 Years" }, "enrollment_count": 120, "start_date": "2026-07-29", "completion_date": "2028-01-31", "has_results": false, "last_update_posted_date": "2026-10-07", "last_synced_at": "2026-11-07T12:07:42.001Z", "location_count": 1, "location_summary": "Honolulu, Hawaii", "locations": [ { "city": "Honolulu", "state": "Hawaii" } ], "official_url": "https://clinicaltrials.gov/study/NCT07038317" } ] }