{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Pre+and+Post+Treatment+Presentations", "query": { "intervention": "Pre and Post Treatment Presentations" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 211, "total_pages": 22, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Pre+and+Post+Treatment+Presentations&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-17T19:29:37.299Z", "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": "NCT04766190", "title": "DISCO: A Patient Intervention to Reduce the Financial Burden of Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Financial Toxicity", "Cancer", "Question Prompt List", "Breast Cancer", "Prostate Cancer" ], "interventions": [ { "name": "Group 2: The DISCO App", "type": "BEHAVIORAL" }, { "name": "Group 1: Usual Care", "type": "BEHAVIORAL" }, { "name": "Group 3: The DISCO App + Booster", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Lauren Hamel", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 254, "start_date": "2021-02-10", "completion_date": "2028-08-31", "has_results": false, "last_update_posted_date": "2026-08-06", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04766190" }, { "nct_id": "NCT05619497", "title": "The OPENS Trial: Offering Women PrEP (Aim 2)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Human Immunodeficiency Virus", "Human Immunodeficiency Virus Transmission", "Sexually Transmitted Diseases" ], "interventions": [ { "name": "Clinic-wide Trainings", "type": "OTHER" }, { "name": "Clinic-wide Trainings and HIV Prevention Decision Support Tool (DST)", "type": "OTHER" }, { "name": "Standard Care with the HIV Prevention Decision Support Tool (DST)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 141, "start_date": "2022-12-02", "completion_date": "2024-11-01", "has_results": false, "last_update_posted_date": "2025-11-25", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05619497" }, { "nct_id": "NCT07053826", "title": "Penile Lengthening Pre-Penile Prosthesis Implantation", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Erectile Dysfunction" ], "interventions": [ { "name": "Penile Traction Device", "type": "DEVICE" }, { "name": "Inflatable Penile Prosthesis Implantation", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "J. Peter Rubin, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 48, "start_date": "2025-08-26", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-09-03", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07053826" }, { "nct_id": "NCT07389278", "title": "Combination ADI-PEG 20, TMZ, and RT for Treatment of Newly Diagnosed High-grade Glioma (HGG)", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Glioblastoma", "High-Grade Glioma (WHO III-IV)", "High-grade Glioma", "Diffuse Midline Glioma, H3 K27M-Mutant", "Diffuse Hemispheric Glioma, H3G34 Mutant" ], "interventions": [ { "name": "ADI-PEG 20 (Arginine deiminase pegylated)", "type": "DRUG" }, { "name": "Temozolomide (TMZ)", "type": "DRUG" }, { "name": "Standard of Care Radiation Therapy (RT)", "type": "RADIATION" } ], "intervention_types": [ "DRUG", "RADIATION" ], "sponsor": "Sabine Mueller, MD, PhD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": "39 Years", "sex": "ALL", "summary": "3 Years to 39 Years" }, "enrollment_count": 97, "start_date": "2027-06-01", "completion_date": "2035-06-30", "has_results": false, "last_update_posted_date": "2026-09-15", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07389278" }, { "nct_id": "NCT07058064", "title": "WATCH (Wearable Artificial inTelligence for Cardiac Function and Health Monitoring)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lymphoma", "Sarcoma" ], "interventions": [ { "name": "Electrocardiogram", "type": "PROCEDURE" }, { "name": "Echocardiogram", "type": "PROCEDURE" }, { "name": "LVEF echocardiogram", "type": "PROCEDURE" }, { "name": "Apple Watch", "type": "OTHER" }, { "name": "Biospecimen collection", "type": "PROCEDURE" }, { "name": "Questionnaires", "type": "OTHER" }, { "name": "Cardio-pulmonary exercise test", "type": "OTHER" }, { "name": "6 minute walk test", "type": "OTHER" }, { "name": "Grip strength test", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2025-07-18", "completion_date": "2029-06-29", "has_results": false, "last_update_posted_date": "2025-10-15", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT07058064" }, { "nct_id": "NCT04031716", "title": "Comprehensive Study of Post-surgical Pain After Pectus or Spine Surgery", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain, Postoperative", "Excavatum, Pectus", "Scoliosis Idiopathic" ], "interventions": [ { "name": "Meditation", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Children's Hospital Medical Center, Cincinnati", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": null, "sex": "ALL", "summary": "8 Years and older" }, "enrollment_count": 600, "start_date": "2018-07-06", "completion_date": "2025-12-31", "has_results": false, "last_update_posted_date": "2025-06-13", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Cincinnati, Ohio", "locations": [ { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT04031716" }, { "nct_id": "NCT06890663", "title": "Telehealth-Delivered Gut-Directed Hypnotherapy for Managing GI Health", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Gastrointestinal Disease", "Gastrointestinal Disorders", "Nervous System" ], "interventions": [ { "name": "Nonspecific Hypnotherapy for Relaxation", "type": "OTHER" }, { "name": "Gut-Directed Hypnotherapy (GDH)", "type": "OTHER" }, { "name": "3-month Follow-Up", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Central Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 11, "start_date": "2025-03-19", "completion_date": "2025-10-30", "has_results": false, "last_update_posted_date": "2025-11-04", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Orlando, Florida", "locations": [ { "city": "Orlando", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06890663" }, { "nct_id": "NCT05056454", "title": "New Moms Mood Tracking & Wellbeing", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Perinatal Depression", "Anxiety", "Pregnancy Related" ], "interventions": [ { "name": "Online therapy with coaching within STAND", "type": "BEHAVIORAL" }, { "name": "Clinical care within STAND", "type": "BEHAVIORAL" }, { "name": "Perinatal Psychiatric Care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "University of California, Los Angeles", "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": 166, "start_date": "2021-04-15", "completion_date": "2024-04-01", "has_results": false, "last_update_posted_date": "2024-07-31", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05056454" }, { "nct_id": "NCT05749939", "title": "Acceptance Commitment Therapy for Caregivers of People with Memory Loss", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Caregiver Burden", "Behavioral and Psychiatric Symptoms of Dementia", "Depressive Symptoms", "Quality of Life", "Psychological Flexibility", "Sleep Quality", "Positive Aspects of Caregiving" ], "interventions": [ { "name": "Acceptance and Commitment Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Utah State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 121, "start_date": "2023-02-16", "completion_date": "2024-01-21", "has_results": false, "last_update_posted_date": "2024-12-06", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "Logan, Utah", "locations": [ { "city": "Logan", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT05749939" }, { "nct_id": "NCT04609683", "title": "Measuring Hydration Levels of Healthy and Heart Failure Patients Before, During, and After an Electrophysiology (EP) Procedure", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiac Arrhythmia" ], "interventions": [ { "name": "AleriTM sensors", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 19, "start_date": "2022-09-19", "completion_date": "2023-11-05", "has_results": false, "last_update_posted_date": "2023-11-29", "last_synced_at": "2026-09-17T19:29:37.299Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04609683" } ] }