{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Survey+and+Questionnaire+Assessment&page=27", "query": { "intervention": "Survey and Questionnaire Assessment", "page": 27 }, "page_size": 10 }, "pagination": { "page": 27, "page_size": 10, "total_count": 1492, "total_pages": 150, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Survey+and+Questionnaire+Assessment&page=28&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Survey+and+Questionnaire+Assessment&page=26&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-22T19:10:34.466Z", "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": "NCT06008990", "title": "Maternal Brain Imaging in Opioid Use Disorder", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Opioid Use Disorder", "Substance-Related Disorders", "Substance Use", "Pregnancy Related", "Narcotic-Related Disorders", "Buprenorphine Dependence" ], "interventions": [ { "name": "Buprenorphine", "type": "DRUG" }, { "name": "Maternal Brain MRI", "type": "DIAGNOSTIC_TEST" }, { "name": "Blood Samples", "type": "OTHER" }, { "name": "Questionnaires", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "DIAGNOSTIC_TEST", "OTHER", "BEHAVIORAL" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "FEMALE", "summary": "18 Years to 100 Years · Female only" }, "enrollment_count": 45, "start_date": "2023-08-15", "completion_date": "2025-10-31", "has_results": false, "last_update_posted_date": "2026-05-22", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT06008990" }, { "nct_id": "NCT03075618", "title": "Acute Pancreatitis Patient Registry To Examine Novel Therapies In Clinical Experiences (APPRENTICE)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Pancreatitis" ], "interventions": [ { "name": "Questionnaires", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 623, "start_date": "2015-07", "completion_date": "2020-03-23", "has_results": false, "last_update_posted_date": "2020-04-06", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03075618" }, { "nct_id": "NCT07032350", "title": "E-Tailored Pain Management Support for Dementia Family Caregivers: Feasibility of the PACE-app", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Care Giving Burden", "Dementia", "Chronic Pain", "Pain Management", "Palliative Care" ], "interventions": [ { "name": "Web-based pain management support tool", "type": "OTHER" }, { "name": "Usual Pain Management Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "University of Iowa", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 60, "start_date": "2025-05-22", "completion_date": "2026-05", "has_results": false, "last_update_posted_date": "2025-06-29", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 1, "location_summary": "Iowa City, Iowa", "locations": [ { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT07032350" }, { "nct_id": "NCT00351988", "title": "Effects of Cancer Symptoms on Caregivers", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Psychosocial" ], "interventions": [ { "name": "Phenomenological Interviews", "type": "BEHAVIORAL" }, { "name": "Quantitative Interviews", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 199, "start_date": "2006-01-26", "completion_date": "2022-01-20", "has_results": false, "last_update_posted_date": "2022-02-16", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 4, "location_summary": "Miami, Florida • Houston, Texas", "locations": [ { "city": "Miami", "state": "Florida" }, { "city": "Houston", "state": "Texas" }, { "city": "Houston", "state": "Texas" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00351988" }, { "nct_id": "NCT00673179", "title": "Doxorubicin With Cisplatin, High-Dose Methotrexate, and Additional Risk-Adapted Outpatient Chemotherapy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteosarcoma" ], "interventions": [ { "name": "Doxorubicin", "type": "DRUG" }, { "name": "Cisplatin", "type": "DRUG" }, { "name": "Methotrexate", "type": "DRUG" }, { "name": "Leucovorin", "type": "DRUG" }, { "name": "Dexrazoxane", "type": "DRUG" }, { "name": "Ifosfamide", "type": "DRUG" }, { "name": "Questionnaire", "type": "BEHAVIORAL" }, { "name": "Gemcitabine", "type": "DRUG" }, { "name": "Sargramostim", "type": "DRUG" }, { "name": "Surgery", "type": "PROCEDURE" }, { "name": "Mesna", "type": "DRUG" } ], "intervention_types": [ "DRUG", "BEHAVIORAL", "PROCEDURE" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "5 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "5 Years to 40 Years" }, "enrollment_count": 7, "start_date": "2008-05", "completion_date": "2010-11", "has_results": true, "last_update_posted_date": "2014-09-10", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00673179" }, { "nct_id": "NCT01144741", "title": "Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Freeman-Sheldon Syndrome", "Arthrogryposis Distal Type 2A", "Whistling Face Syndrome", "Craniocarpotarsal Dysplasia", "Craniocarpotarsal Dystrophy", "Freeman-Sheldon Syndrome Variant", "Sheldon-Hall Syndrome", "Arthrogryposis Distal Type 2B", "Gordon Syndrome", "Arthrogryposis Distal Type 3", "Arthrogryposis Distal Type 1", "Arthrogryposis, Distal, Type 1A", "Arthrogryposis Distal Type 1B", "Arthrogryposis, Distal", "Craniofacial Abnormalities", "Arthrogryposis" ], "interventions": [ { "name": "PTSD Checklist-Civilian (PCL-C)", "type": "OTHER" }, { "name": "Modified Flanagan Quality of Life Scale", "type": "OTHER" }, { "name": "Center for Epidemiologic Studies Depression Scale (CES-D)", "type": "OTHER" }, { "name": "Functional Enquiry (or Review of Systems) Form", "type": "OTHER" }, { "name": "Study of Therapeutic Outcomes and Practices in Freeman-Sheldon Syndrome (STOP-FSS) Questionnaire", "type": "OTHER" }, { "name": "FSRG Semi-Structured Quality of Life Interview (FSRG SSQLI)", "type": "OTHER" }, { "name": "Medical Records Review", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Freeman-Sheldon Research Group, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 2, "start_date": "2010-02", "completion_date": "2022-06-14", "has_results": false, "last_update_posted_date": "2022-06-21", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 1, "location_summary": "Buckhannon, West Virginia", "locations": [ { "city": "Buckhannon", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01144741" }, { "nct_id": "NCT03930524", "title": "Adaptive Preventive Intervention for College Alcohol Use", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "College Student Drinking" ], "interventions": [ { "name": "Personalized Normative Feedback (PNF)", "type": "BEHAVIORAL" }, { "name": "Self-Monitoring (SM)", "type": "BEHAVIORAL" }, { "name": "Web-BASICS", "type": "BEHAVIORAL" }, { "name": "Health Promotion Consultation", "type": "BEHAVIORAL" }, { "name": "M-Bridge Online Health Coach", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "18 Years to 21 Years" }, "enrollment_count": 891, "start_date": "2019-07-31", "completion_date": "2022-08-01", "has_results": true, "last_update_posted_date": "2023-04-12", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03930524" }, { "nct_id": "NCT00605670", "title": "Measuring Patient Satisfaction and Quality of Life Following Body Image Altering Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer", "Breast Surgery", "Breast Reconstruction", "Breast Reduction", "Breast Augmentation" ], "interventions": [ { "name": "questionnaires", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 722, "start_date": "2005-06", "completion_date": "2013-11", "has_results": false, "last_update_posted_date": "2013-11-14", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 4, "location_summary": "Baltimore, Maryland • Lebanon, New Hampshire • New York, New York + 1 more", "locations": [ { "city": "Baltimore", "state": "Maryland" }, { "city": "Lebanon", "state": "New Hampshire" }, { "city": "New York", "state": "New York" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00605670" }, { "nct_id": "NCT04138810", "title": "Postoperative Virtual Clinical Encounters", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pelvic Organ Prolapse" ], "interventions": [ { "name": "VCE", "type": "OTHER" }, { "name": "Survey", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Pennsylvania", "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": 54, "start_date": "2017-07-17", "completion_date": "2019-07-01", "has_results": true, "last_update_posted_date": "2020-08-24", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04138810" }, { "nct_id": "NCT02554968", "title": "Reliability and Validity of Patient Reported Outcome Measures in Head and Neck Cancer", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Shoulder Pain", "Head and Neck Cancer" ], "interventions": [ { "name": "Questionnaires", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 182, "start_date": "2015-09", "completion_date": "2017-09", "has_results": false, "last_update_posted_date": "2018-07-06", "last_synced_at": "2026-10-22T19:10:34.466Z", "location_count": 3, "location_summary": "Phoenix, Arizona • Jacksonville, Florida • Rochester, Minnesota", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02554968" } ] }