{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Survey+completion&page=14", "query": { "intervention": "Survey completion", "page": 14 }, "page_size": 10 }, "pagination": { "page": 14, "page_size": 10, "total_count": 2371, "total_pages": 238, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Survey+completion&page=15&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Survey+completion&page=13&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-21T19:17:27.280Z", "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": "NCT01846286", "title": "Neuropathic Pain in Head and Neck Cancer", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Head and Neck Cancer" ], "interventions": [ { "name": "Questionnaires", "type": "BEHAVIORAL" }, { "name": "Quantitative Sensory Testing", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "M.D. Anderson 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": 838, "start_date": "2012-10-15", "completion_date": "2022-12-31", "has_results": false, "last_update_posted_date": "2022-05-25", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 2, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01846286" }, { "nct_id": "NCT04375462", "title": "AspireAssist for Palliative Venting Gastrostomy in Malignant Bowel Obstruction Patients", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Malignant Small Bowel Obstruction", "Malignant Gastric Outlet Obstruction" ], "interventions": [ { "name": "AspireAssist device", "type": "DEVICE" }, { "name": "Standard decompressive PEG tube", "type": "DEVICE" }, { "name": "gastric outlet obstruction scoring system (GOOSS) questionnaire", "type": "OTHER" }, { "name": "Modified Gastroparesis Cardinal Symptom Index (GCSI) questionnaire", "type": "OTHER" }, { "name": "Patient satisfaction and ease of use survey", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Case Comprehensive 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": 0, "start_date": "2023-02-01", "completion_date": "2023-08-01", "has_results": false, "last_update_posted_date": "2023-01-31", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT04375462" }, { "nct_id": "NCT07455370", "title": "A Study of Moral Distress, Moral Injury and Post-Traumatic Stress for Nurses", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Moral Injury", "Moral Distress", "Post-Traumatic Stress", "Nurse Well-being", "Wellbeing", "Wellness, Psychological", "Wellness", "Nurses", "Nurse Health" ], "interventions": [ { "name": "Surveys", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 21300, "start_date": "2026-03-03", "completion_date": "2026-11", "has_results": false, "last_update_posted_date": "2026-09-17", "last_synced_at": "2026-10-21T19:17:27.280Z", "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/NCT07455370" }, { "nct_id": "NCT07339254", "title": "Experiences w/ & Attitudes Towards Immune Chckpt Inhibitors in NSCLC Patients Single Center Survey Based Study", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Lung Non-Small Cell Carcinoma" ], "interventions": [ { "name": "Non-Interventional Study", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Southern California", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2026-03-12", "completion_date": "2028-03-12", "has_results": false, "last_update_posted_date": "2026-03-16", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 2, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07339254" }, { "nct_id": "NCT04600466", "title": "Molecular and Epidemiological Risk Factors in the Development of Gastric Cancer", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Gastric Cancer" ], "interventions": [ { "name": "Molecular testing for all participants.", "type": "OTHER" }, { "name": "Germline Testing", "type": "OTHER" }, { "name": "Survey", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The University of Texas Health Science Center at San Antonio", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 129, "start_date": "2021-01-22", "completion_date": "2025-06-06", "has_results": false, "last_update_posted_date": "2026-04-14", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04600466" }, { "nct_id": "NCT07293403", "title": "Duvelisib Maintenance for the Treatment of Peripheral T-Cell Lymphomas", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Follicular Helper T-Cell Lymphoma", "Peripheral T-Cell Lymphoma, Not Otherwise Specified" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Bone Marrow Aspiration", "type": "PROCEDURE" }, { "name": "Bone Marrow Biopsy", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Duvelisib", "type": "DRUG" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "DRUG", "OTHER" ], "sponsor": "City of Hope Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 25, "start_date": "2026-08-03", "completion_date": "2028-09-17", "has_results": false, "last_update_posted_date": "2026-10-19", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 1, "location_summary": "Duarte, California", "locations": [ { "city": "Duarte", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07293403" }, { "nct_id": "NCT00581724", "title": "Pain in Cancer Survivors", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer", "Colorectal Cancer", "Prostate Cancer", "Head and Neck Cancer", "Lung Cancer" ], "interventions": [ { "name": "Telephone interview or self report survey.", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "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": 200, "start_date": "2007-05", "completion_date": "2012-01", "has_results": false, "last_update_posted_date": "2012-01-26", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00581724" }, { "nct_id": "NCT05926024", "title": "Long-Term Follow-Up in Women With Early Breast Cancer Three Years of More Post Primary Treatment", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Exercise Recall Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Health Behavior Questionnaire (HBQ)30 Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Functional Assessment of Cancer Therapy-General (FACT-G) Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) Patient Reported Outcomes", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PROMIS Cognitive Function (Short Form 8a)", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Functional Assessment of Cancer-Gynecology Oncology Group-Neurotoxicity (FACT/GOG-NTX-12)", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PROMIS", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes FACT-Endocrine Symptoms", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes Penn Arthralgia Aging Survey", "type": "BEHAVIORAL" }, { "name": "Patient Reported Outcomes PRO-CTCAE (patient-reported CTCAE)", "type": "BEHAVIORAL" }, { "name": "p16 tumor suppressor gene", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "BEHAVIORAL", "DIAGNOSTIC_TEST" ], "sponsor": "UNC Lineberger Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 253, "start_date": "2023-01-06", "completion_date": "2028-01-31", "has_results": false, "last_update_posted_date": "2026-03-11", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05926024" }, { "nct_id": "NCT03656224", "title": "Survey of Post-Acute Inpatient Rehabilitation Safety Concerns in Participants With Cancer", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Malignant Neoplasm" ], "interventions": [ { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "M.D. Anderson 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": 261, "start_date": "2018-08-29", "completion_date": "2021-08-16", "has_results": false, "last_update_posted_date": "2021-08-23", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03656224" }, { "nct_id": "NCT04376710", "title": "Surgical Telemedicine in the COVID-19 Pandemic Era", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "COVID", "Surgery" ], "interventions": [ { "name": "Completion of pre-pandemic survey", "type": "OTHER" }, { "name": "Completion of survey after peak of pandemic", "type": "OTHER" }, { "name": "Completion of post telemedicine encounter survey", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "31 Days", "maximum_age": "18 Years", "sex": "ALL", "summary": "31 Days to 18 Years" }, "enrollment_count": 180, "start_date": "2020-07-01", "completion_date": "2020-10-01", "has_results": false, "last_update_posted_date": "2020-10-28", "last_synced_at": "2026-10-21T19:17:27.280Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04376710" } ] }