{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Enhanced+Choice&page=4", "query": { "intervention": "Enhanced Choice", "page": 4 }, "page_size": 10 }, "pagination": { "page": 4, "page_size": 10, "total_count": 336, "total_pages": 34, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Enhanced+Choice&page=5&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Enhanced+Choice&page=3&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-27T03:52:26.270Z", "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": "NCT03373916", "title": "Peer Mentorship to Reduce Suicide Attempts Among High-Risk Adults", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicidal Ideation" ], "interventions": [ { "name": "Peer mentorship", "type": "BEHAVIORAL" }, { "name": "Enhanced Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 455, "start_date": "2018-06-22", "completion_date": "2023-09-30", "has_results": true, "last_update_posted_date": "2025-04-30", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 3, "location_summary": "Ann Arbor, Michigan • Ferndale, Michigan • Mount Clemens, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Ferndale", "state": "Michigan" }, { "city": "Mount Clemens", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03373916" }, { "nct_id": "NCT05780814", "title": "The Effects of Treating Insomnia on Behavioral Weight Loss Outcomes in Survivors of Breast Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Insomnia", "Weight Gain" ], "interventions": [ { "name": "Cognitive-Behavioral Therapy for Insomnia (CBT-I)", "type": "BEHAVIORAL" }, { "name": "Sleep Education Control (EDU)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Johns Hopkins University", "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": 250, "start_date": "2024-02-01", "completion_date": "2028-12-31", "has_results": false, "last_update_posted_date": "2026-02-23", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 4, "location_summary": "Washington D.C., District of Columbia • Baltimore, Maryland • Lutherville, Maryland", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "Lutherville", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT05780814" }, { "nct_id": "NCT04983498", "title": "Enhanced Recovery Pathway for Endoscopy", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Enhanced Recovery Pathway", "Endoscopy" ], "interventions": [ { "name": "Ondansetron 4 MG", "type": "DRUG" }, { "name": "Lactated Ringers, Intravenous", "type": "DRUG" }, { "name": "Early Mobilization", "type": "OTHER" }, { "name": "Early PO Intake", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2021-09-01", "completion_date": "2022-01-01", "has_results": false, "last_update_posted_date": "2021-12-15", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04983498" }, { "nct_id": "NCT06969521", "title": "Online Rotating Delivery of Perception/Production Enhanced Treatment for Rhotics", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Speech Sound Disorder" ], "interventions": [ { "name": "Visual acoustic biofeedback: ORDER", "type": "BEHAVIORAL" }, { "name": "Perception Training: ORDER", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Montclair State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "8 Years to 17 Years" }, "enrollment_count": 60, "start_date": "2025-05-10", "completion_date": "2027-07-01", "has_results": false, "last_update_posted_date": "2026-08-28", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 1, "location_summary": "Montclair, New Jersey", "locations": [ { "city": "Montclair", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT06969521" }, { "nct_id": "NCT00820001", "title": "Resources to Enhance the Adjustment of Children (REACH)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Oppositional Defiant Disorder", "Conduct Disorder", "Attention Deficit Hyperactivity Disorder" ], "interventions": [ { "name": "Booster Treatment", "type": "BEHAVIORAL" }, { "name": "No-Booster", "type": "BEHAVIORAL" }, { "name": "No intervention", "type": "OTHER" }, { "name": "Treatment As Usual", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "6 Years", "maximum_age": "11 Years", "sex": "ALL", "summary": "6 Years to 11 Years" }, "enrollment_count": 254, "start_date": "2003-12", "completion_date": "2009-11", "has_results": false, "last_update_posted_date": "2013-02-18", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 2, "location_summary": "Cincinnati, Ohio • Pittsburgh, Pennsylvania", "locations": [ { "city": "Cincinnati", "state": "Ohio" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00820001" }, { "nct_id": "NCT03952637", "title": "A Phase 1/2 Study of Intravenous Gene Transfer With an AAV9 Vector Expressing Human Beta-galactosidase in Type I and Type II GM1 Gangliosidosis", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Lysosomal Diseases", "Gangliosidosis", "GM1" ], "interventions": [ { "name": "AAV9-GLB1", "type": "BIOLOGICAL" }, { "name": "Abdominal ultrasound", "type": "PROCEDURE" }, { "name": "Rituximab", "type": "DRUG" }, { "name": "Sirolimus", "type": "DRUG" }, { "name": "Methylprednisolone", "type": "DRUG" }, { "name": "Prednisone", "type": "DRUG" }, { "name": "Audiology assessment with ABR", "type": "DIAGNOSTIC_TEST" }, { "name": "Bone density scan (DEXA)", "type": "DIAGNOSTIC_TEST" }, { "name": "Electrocardiogram (EKG)", "type": "DIAGNOSTIC_TEST" }, { "name": "Echocardiogram", "type": "DIAGNOSTIC_TEST" }, { "name": "Electroencephalogram (EEG) awake and extended overnight", "type": "OTHER" }, { "name": "Laboratory tests", "type": "DIAGNOSTIC_TEST" }, { "name": "Lumbar puncture", "type": "PROCEDURE" }, { "name": "Brain MRI/MRS/fMRI", "type": "PROCEDURE" }, { "name": "Neurocognitive testing", "type": "BEHAVIORAL" }, { "name": "Neurology exam", "type": "OTHER" }, { "name": "PICC or other Central line placement", "type": "BEHAVIORAL" }, { "name": "Skeletal survey", "type": "PROCEDURE" }, { "name": "Skin biopsy", "type": "PROCEDURE" }, { "name": "Speech and modified barium swallow study", "type": "PROCEDURE" }, { "name": "Ophthalmology exam", "type": "PROCEDURE" } ], "intervention_types": [ "BIOLOGICAL", "PROCEDURE", "DRUG", "DIAGNOSTIC_TEST", "OTHER", "BEHAVIORAL" ], "sponsor": "National Human Genome Research Institute (NHGRI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "6 Months", "maximum_age": "12 Years", "sex": "ALL", "summary": "6 Months to 12 Years" }, "enrollment_count": 54, "start_date": "2019-08-19", "completion_date": "2030-01-01", "has_results": false, "last_update_posted_date": "2026-09-21", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT03952637" }, { "nct_id": "NCT07494812", "title": "Examining the Feasibility of Using Pressure Gradient Regulated Automated Cerebral Spinal Fluid Drainage During External Lumbar Drain Trials", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "NPH (Normal Pressure Hydrocephalus)" ], "interventions": [ { "name": "Intellidrop Automated CSF Drainage System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Texas Southwestern Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "60 Years to 99 Years" }, "enrollment_count": 10, "start_date": "2026-05-14", "completion_date": "2026-10-31", "has_results": false, "last_update_posted_date": "2026-06-02", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07494812" }, { "nct_id": "NCT07074145", "title": "WEAVE NM: Heart Health and Nutrition for Life", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension" ], "interventions": [ { "name": "Heart Health and Nutrition for Life (HHNL)", "type": "BEHAVIORAL" }, { "name": "Self-Measured Blood Pressure", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of New Mexico", "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": 240, "start_date": "2025-02-21", "completion_date": "2027-11-30", "has_results": false, "last_update_posted_date": "2026-07-30", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 1, "location_summary": "Albuquerque, New Mexico", "locations": [ { "city": "Albuquerque", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT07074145" }, { "nct_id": "NCT05870176", "title": "ActivityChoice: Implementing Clinic-Based Physical Activity Program Choices for Cancer Survivors", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Cardiovascular Diseases", "Physical Inactivity" ], "interventions": [ { "name": "Enhanced Referral", "type": "BEHAVIORAL" }, { "name": "Standard Referral", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Massachusetts, Worcester", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "110 Years", "sex": "ALL", "summary": "18 Years to 110 Years" }, "enrollment_count": 114, "start_date": "2023-09-11", "completion_date": "2027-03-01", "has_results": false, "last_update_posted_date": "2026-08-31", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 1, "location_summary": "Worcester, Massachusetts", "locations": [ { "city": "Worcester", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05870176" }, { "nct_id": "NCT06392607", "title": "Euclid Phoenix Lens Design Trial 2", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Myopia", "Cornea" ], "interventions": [ { "name": "Euclid orthokeratology (standard coating)", "type": "DEVICE" }, { "name": "Euclid orthokeratology (enhanced coating)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Euclid Systems Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "6 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "6 Years to 35 Years" }, "enrollment_count": 50, "start_date": "2024-05", "completion_date": "2025-09", "has_results": false, "last_update_posted_date": "2024-04-30", "last_synced_at": "2026-10-27T03:52:26.270Z", "location_count": 5, "location_summary": "Edina, Minnesota • Sartell, Minnesota • North Brunswick, New Jersey + 2 more", "locations": [ { "city": "Edina", "state": "Minnesota" }, { "city": "Sartell", "state": "Minnesota" }, { "city": "North Brunswick", "state": "New Jersey" }, { "city": "Memphis", "state": "Tennessee" }, { "city": "Kirkland", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06392607" } ] }