{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Parent+Survey", "query": { "intervention": "Parent Survey" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 294, "total_pages": 30, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Parent+Survey&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-06T21:31:40.882Z", "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": "NCT02675933", "title": "Satisfaction Rates Among Parents of Children With Autism in the ED", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Autism Spectrum Disorder" ], "interventions": [ { "name": "Questionnaire", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Seton Healthcare Family", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "2 Years to 18 Years" }, "enrollment_count": 63, "start_date": "2016-02", "completion_date": "2017-01-06", "has_results": true, "last_update_posted_date": "2024-12-09", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02675933" }, { "nct_id": "NCT06002282", "title": "HPV Vaccine Confident Families", "overall_status": "SUSPENDED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Human Papillomavirus Vaccines" ], "interventions": [ { "name": "Tailored messages", "type": "BEHAVIORAL" }, { "name": "Standard messages", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rutgers, The State University of New Jersey", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 70, "start_date": "2025-10", "completion_date": "2026-07", "has_results": false, "last_update_posted_date": "2025-08-11", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "New Brunswick, New Jersey", "locations": [ { "city": "New Brunswick", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT06002282" }, { "nct_id": "NCT04959188", "title": "Needs Assessment for Individuals and Families Affected by Dyskeratosis Congenita (DC) and Related Telomere Biology Disorders (TBD)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Dyskeratosis Congenita", "Telomere Biology Disorders" ], "interventions": [], "intervention_types": [], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 53, "start_date": "2021-09-09", "completion_date": "2023-07-05", "has_results": false, "last_update_posted_date": "2024-12-11", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT04959188" }, { "nct_id": "NCT07412002", "title": "Quality of End-of-Life Care for Children With Cancer", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Childhood Hematopoietic and Lymphatic System Neoplasm", "Childhood Malignant Solid Neoplasm" ], "interventions": [ { "name": "Non-Interventional Study", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Children's Oncology Group", "sponsor_class": "NETWORK", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2425, "start_date": "2026-07-31", "completion_date": "2031-01-31", "has_results": false, "last_update_posted_date": "2026-09-04", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 28, "location_summary": "Birmingham, Alabama • Little Rock, Arkansas • Oakland, California + 25 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Oakland", "state": "California" }, { "city": "Wilmington", "state": "Delaware" }, { "city": "Fort Myers", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07412002" }, { "nct_id": "NCT06652880", "title": "Digital Support Intervention for Pregnant People with Opioid Use Disorders", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Digital Intervention", "Bibliotherapy" ], "interventions": [ { "name": "Digital technology", "type": "DEVICE" }, { "name": "Bibliotherapy", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 32, "start_date": "2024-06-04", "completion_date": "2025-12-31", "has_results": false, "last_update_posted_date": "2025-02-17", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06652880" }, { "nct_id": "NCT07155083", "title": "Firearm Safety Survey", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Firearm Ownership" ], "interventions": [ { "name": "Survey using a questionnaire.", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Vanessa Ng", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 1000, "start_date": "2025-09-16", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2025-11-03", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07155083" }, { "nct_id": "NCT03974737", "title": "CRI in POTS in Adolescents", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Postural Orthostatic Tachycardia Syndrome" ], "interventions": [ { "name": "CRI device (non-invasive vitals sign measurement)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "12 Years to 21 Years" }, "enrollment_count": 77, "start_date": "2019-06-01", "completion_date": "2020-09-22", "has_results": false, "last_update_posted_date": "2021-01-26", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT03974737" }, { "nct_id": "NCT06689800", "title": "Let's Get REAL: Family Health Communication Tool in Pediatric Stem Cell Transplant and Cellular Therapy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hematologic Malignancy", "Solid Tumor", "Sickle Cell Disease", "Aplastic Anemia", "Immune Deficiency", "Metabolic Disorder" ], "interventions": [ { "name": "Let's Get REAL", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": null, "sex": "ALL", "summary": "8 Years and older" }, "enrollment_count": 60, "start_date": "2024-11-26", "completion_date": "2026-11-30", "has_results": false, "last_update_posted_date": "2026-06-04", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT06689800" }, { "nct_id": "NCT05582551", "title": "Patients At Risk for Sensory Screening (HPARSS) to Enhance Sensory Deficit Screening in Childhood Cancer Survivors", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Childhood Cancer" ], "interventions": [ { "name": "Highlighting Patients at Risk for Sensory Screening (HPARSS)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Washington University School of Medicine", "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": 146, "start_date": "2023-08-02", "completion_date": "2027-05-31", "has_results": false, "last_update_posted_date": "2026-06-15", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05582551" }, { "nct_id": "NCT03666429", "title": "Effectiveness of the NoseFrida Compared With Bulb Suction at Relieving Objective Signs of Nasal Obstruction and Reducing Return Visits in Pediatric Patients Presenting to the Emergency Department", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Upper Respiratory Tract Infections", "Nasal Suction", "Return Emergency Department Visits" ], "interventions": [ { "name": "Bulb suction", "type": "DEVICE" }, { "name": "NoseFrida", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Day", "maximum_age": "24 Months", "sex": "ALL", "summary": "1 Day to 24 Months" }, "enrollment_count": 0, "start_date": "2020-01-01", "completion_date": "2020-11", "has_results": false, "last_update_posted_date": "2020-12-03", "last_synced_at": "2026-09-06T21:31:40.882Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT03666429" } ] }