{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Pre-assessment+questionnaire&page=2", "query": { "intervention": "Pre-assessment questionnaire", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Pre-assessment+questionnaire&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-27T20:36:48.617Z", "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": "NCT07795801", "title": "Mind-Body Sexual Well-Being Program for Female GI Cancer Survivors", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colorectal Cancer (Diagnosis)", "Anal Cancer", "Sexual Dysfunction Female" ], "interventions": [ { "name": "Mind-Body Group Intervention", "type": "BEHAVIORAL" }, { "name": "Enhanced Usual Care Control (EUCC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "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": 100, "start_date": "2026-10-01", "completion_date": "2029-06-01", "has_results": false, "last_update_posted_date": "2026-09-08", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07795801" }, { "nct_id": "NCT03163901", "title": "The Effect of OMT on Functional Outcomes and Anti-inflammatory Biomarkers in Mild to Moderate Traumatic Brain Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vestibular Disorder", "Headache", "Traumatic Brain Injury" ], "interventions": [ { "name": "Osteopathic Manipulative Treatment", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Michigan 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": 29, "start_date": "2017-09-18", "completion_date": "2020-02-29", "has_results": false, "last_update_posted_date": "2020-06-24", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 1, "location_summary": "Mason, Michigan", "locations": [ { "city": "Mason", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03163901" }, { "nct_id": "NCT03043300", "title": "A Pilot Study Assessing Intestinal Microbiota Diversification and Changes After Travel to South(East) Asia From the US", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Dysbiosis" ], "interventions": [ { "name": "Screening Criteria Review", "type": "OTHER" }, { "name": "Pre-Travel Questionnaire", "type": "OTHER" }, { "name": "Pre-Travel Stool Specimen Collection", "type": "OTHER" }, { "name": "Short-Term Post-Travel Questionnaire", "type": "OTHER" }, { "name": "Short-Term Post-Travel Stool Specimen Collection", "type": "OTHER" }, { "name": "Long-Term Post-Travel Questionnaire", "type": "OTHER" }, { "name": "Long-Term Post-Travel Stool Specimen Collection", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 10, "start_date": "2017-11-07", "completion_date": "2018-12-01", "has_results": false, "last_update_posted_date": "2019-01-30", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 2, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03043300" }, { "nct_id": "NCT02942212", "title": "Health Literacy and Smoking Cessation in Low-SES Diverse Smokers - Project HALT II", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Smoking Cessation" ], "interventions": [ { "name": "Questionnaire", "type": "BEHAVIORAL" }, { "name": "In-Depth Interviews", "type": "BEHAVIORAL" }, { "name": "Breath Test", "type": "OTHER" }, { "name": "Nicotine Patches", "type": "DRUG" }, { "name": "Advice plus Phone Counseling", "type": "BEHAVIORAL" }, { "name": "Advice plus Counseling Sessions", "type": "BEHAVIORAL" }, { "name": "Self Assessment Questionnaires", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "DRUG" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "25 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "25 Years to 65 Years" }, "enrollment_count": 0, "start_date": "2018-12-14", "completion_date": "2018-12-14", "has_results": false, "last_update_posted_date": "2019-05-01", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02942212" }, { "nct_id": "NCT04214067", "title": "Testing the Addition of the Immunotherapy Drug, Pembrolizumab, to the Usual Radiation Treatment for Newly Diagnosed Early Stage High Intermediate Risk Endometrial Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Endometrial Endometrioid Adenocarcinoma", "Stage I Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8", "Stage II Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Brachytherapy", "type": "RADIATION" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "External Beam Radiation Therapy", "type": "RADIATION" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Pembrolizumab", "type": "BIOLOGICAL" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "X-Ray Imaging", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "RADIATION", "BIOLOGICAL", "OTHER" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 164, "start_date": "2020-04-09", "completion_date": "2027-02-05", "has_results": false, "last_update_posted_date": "2026-07-02", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 275, "location_summary": "Birmingham, Alabama • Clovis, California • Concord, California + 195 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Clovis", "state": "California" }, { "city": "Clovis", "state": "California" }, { "city": "Concord", "state": "California" }, { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04214067" }, { "nct_id": "NCT05135260", "title": "Virtual Reality on Pain, Stress, and Affect in the Infusion Clinic", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Chemotherapy" ], "interventions": [ { "name": "Virtual reality therapy", "type": "BEHAVIORAL" }, { "name": "Questionnaires", "type": "BEHAVIORAL" }, { "name": "Measure heart rate", "type": "PROCEDURE" }, { "name": "Cyber sickness measurement", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL", "PROCEDURE" ], "sponsor": "Cody Stansel", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 99, "start_date": "2021-11-01", "completion_date": "2023-12-16", "has_results": false, "last_update_posted_date": "2024-10-16", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT05135260" }, { "nct_id": "NCT04497961", "title": "A Study of Health-Related Quality of Life in People With Multiple Myeloma Receiving Daratumumab or Lenalidomide", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Multiple Myeloma" ], "interventions": [ { "name": "Lenalidomide", "type": "DRUG" }, { "name": "Daratumumab", "type": "DRUG" }, { "name": "Questionnaires", "type": "BEHAVIORAL" }, { "name": "Dietary Intervention", "type": "OTHER" } ], "intervention_types": [ "DRUG", "BEHAVIORAL", "OTHER" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 95, "start_date": "2020-08-28", "completion_date": "2027-08", "has_results": false, "last_update_posted_date": "2026-09-15", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 7, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Montvale, New Jersey + 4 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04497961" }, { "nct_id": "NCT04769960", "title": "Study of the Safety of MRI Scans in People Who Have Breast Tissue Expanders After Mastectomy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer", "Breast Neoplasms", "Breast Adenocarcinoma" ], "interventions": [ { "name": "MRI Studies", "type": "DIAGNOSTIC_TEST" }, { "name": "Patient Reported Outcomes", "type": "BEHAVIORAL" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering 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": 68, "start_date": "2021-02-19", "completion_date": "2027-02-19", "has_results": false, "last_update_posted_date": "2026-05-18", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 3, "location_summary": "Montvale, New Jersey • Commack, New York • New York, New York", "locations": [ { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04769960" }, { "nct_id": "NCT03534934", "title": "CT-Based Modeling of Bone Micro-Architecture and Fracture-Risk in COPD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pulmonary Disease, Chronic Obstructive", "Osteoporosis" ], "interventions": [ { "name": "Vital signs", "type": "DIAGNOSTIC_TEST" }, { "name": "Urine Pregnancy Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Questionnaires", "type": "OTHER" }, { "name": "Blood Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Duel-energy X-ray absorptiometry scan", "type": "DIAGNOSTIC_TEST" }, { "name": "Multi-detector computed tomography", "type": "DIAGNOSTIC_TEST" }, { "name": "Dual-energy X-ray absorptiometry scan", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER" ], "sponsor": "Punam K Saha", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "45 Years to 90 Years" }, "enrollment_count": 560, "start_date": "2019-02-26", "completion_date": "2025-03-19", "has_results": false, "last_update_posted_date": "2026-01-28", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 2, "location_summary": "Iowa City, Iowa • New York, New York", "locations": [ { "city": "Iowa City", "state": "Iowa" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03534934" }, { "nct_id": "NCT01491698", "title": "Impact of Roux-En-Y Pouch Reconstruction Compared With Conventional Roux-En-Y Reconstruction on Health-Related Quality of Life in Patients Undergoing Total Gastrectomy for Adenocarcinoma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Gastric Cancer" ], "interventions": [ { "name": "Roux-en-Y pouch reconstruction (RYP)", "type": "PROCEDURE" }, { "name": "conventional Roux-en-Y reconstruction (RYC)", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 12, "start_date": "2011-12", "completion_date": "2013-08", "has_results": false, "last_update_posted_date": "2013-08-15", "last_synced_at": "2026-09-27T20:36:48.617Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01491698" } ] }