{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Questionnaires+%26+Study+Visit", "query": { "intervention": "Questionnaires & Study Visit" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 599, "total_pages": 60, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Questionnaires+%26+Study+Visit&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-09T10:14:26.137Z", "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": "NCT05671861", "title": "Evaluating a Low-Cost Therapeutic Device in Managing Head and Neck Cancer Patients With Radiation-Related Trismus", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Trismus", "Head and Neck Cancer" ], "interventions": [ { "name": "Trismus Device Prototype", "type": "DEVICE" }, { "name": "Questionnaires", "type": "OTHER" }, { "name": "Mobile Application", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 35, "start_date": "2023-04-27", "completion_date": "2028-03-31", "has_results": false, "last_update_posted_date": "2026-01-13", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05671861" }, { "nct_id": "NCT03514680", "title": "Clinician Decision Support Algorithm for Chemotherapy-Induced Peripheral Neuropathy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Chemotherapy-induced Peripheral Neuropathy" ], "interventions": [ { "name": "CIPN Assessment and Management Algorithm", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Dana-Farber Cancer Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 226, "start_date": "2018-06-04", "completion_date": "2020-03-23", "has_results": false, "last_update_posted_date": "2022-03-16", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03514680" }, { "nct_id": "NCT04954313", "title": "Baseline Oral Health Study: UnCoVer the Connections to General Health", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cardiovascular Diseases", "Diabetes Type 2" ], "interventions": [ { "name": "Subgingival chlorhexidine irrigation", "type": "DRUG" }, { "name": "Dental Supplies", "type": "OTHER" }, { "name": "Periodonal Treatment", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 786, "start_date": "2021-09-28", "completion_date": "2025-02-01", "has_results": true, "last_update_posted_date": "2026-02-12", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 2, "location_summary": "Chapel Hill, North Carolina • Kannapolis, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" }, { "city": "Kannapolis", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04954313" }, { "nct_id": "NCT06451341", "title": "IMplementation of CAB+RPV LA for People With HIV in Non-Metropolitan Areas", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "HIV" ], "interventions": [ { "name": "Acceptability of Intervention Measure (AIM)", "type": "BEHAVIORAL" }, { "name": "Intervention Appropriateness Measure (IAM)", "type": "BEHAVIORAL" }, { "name": "Feasibility of Intervention Measure (FIM)", "type": "BEHAVIORAL" }, { "name": "HIV Stigma Scale Questionnaire", "type": "BEHAVIORAL" }, { "name": "HIV Treatment Satisfaction Questionnaire status version (HIVTSQs12)", "type": "BEHAVIORAL" }, { "name": "HIV Treatment Satisfaction Questionnaire change version (HIVTSQc12)", "type": "BEHAVIORAL" }, { "name": "Needs and Barriers Assessment", "type": "BEHAVIORAL" }, { "name": "Pre-visit Outreach", "type": "BEHAVIORAL" }, { "name": "Qualitative interview - patient participants", "type": "BEHAVIORAL" }, { "name": "Staff education", "type": "BEHAVIORAL" }, { "name": "Staff Month 7 and 15 Survey - Staff Burden and Engagement", "type": "BEHAVIORAL" }, { "name": "Qualitative interview - staff", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Nebraska", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": null, "sex": "ALL", "summary": "19 Years and older" }, "enrollment_count": 75, "start_date": "2024-07-01", "completion_date": "2028-05", "has_results": false, "last_update_posted_date": "2026-07-24", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 4, "location_summary": "Harlan, Iowa • Shenandoah, Iowa • Grand Island, Nebraska + 1 more", "locations": [ { "city": "Harlan", "state": "Iowa" }, { "city": "Shenandoah", "state": "Iowa" }, { "city": "Grand Island", "state": "Nebraska" }, { "city": "Omaha", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT06451341" }, { "nct_id": "NCT02703532", "title": "Evaluation of a CarePartner-Integrated Telehealth Rehabilitation Program for Persons With Stroke", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke" ], "interventions": [ { "name": "CARE-CITE Education Program", "type": "BEHAVIORAL" }, { "name": "Traditional Education", "type": "BEHAVIORAL" }, { "name": "Constraint-Induced Movement Therapy (CIMT)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 64, "start_date": "2016-01", "completion_date": "2019-01-18", "has_results": true, "last_update_posted_date": "2020-01-28", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02703532" }, { "nct_id": "NCT05444205", "title": "The Pittsburgh Study Early Childhood", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Child Development", "Child Language", "Child Behavior Problem", "Parenting", "Parent Child Abuse" ], "interventions": [ { "name": "Text4Baby or Bright by Text Referral", "type": "BEHAVIORAL" }, { "name": "Nurture Program Warm Referral", "type": "BEHAVIORAL" }, { "name": "Video Interaction Project", "type": "BEHAVIORAL" }, { "name": "Family Check-UP", "type": "BEHAVIORAL" }, { "name": "Smart Beginnings", "type": "BEHAVIORAL" }, { "name": "Healthy Families America Warm Referral", "type": "BEHAVIORAL" }, { "name": "Family Center Warm Referral", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": "6 Years", "sex": "ALL", "summary": "Up to 6 Years" }, "enrollment_count": 24000, "start_date": "2020-06-02", "completion_date": "2031-12", "has_results": false, "last_update_posted_date": "2025-12-03", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 5, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05444205" }, { "nct_id": "NCT02347670", "title": "Comparison Study of Glaucoma Eye Care Follow-Up Adherence in a High Risk Population", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glaucoma" ], "interventions": [ { "name": "Efficacy-patient navigator to improve follow-up adherence", "type": "BEHAVIORAL" }, { "name": "Office-Based Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Wills Eye", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 155, "start_date": "2014-08", "completion_date": "2015-12", "has_results": false, "last_update_posted_date": "2023-12-13", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02347670" }, { "nct_id": "NCT04544683", "title": "Effectiveness of Cervical Transforaminal Epidural Steroid Injection", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cervical Radiculopathy", "Cervical Spondylosis", "Disk, Herniated" ], "interventions": [ { "name": "Cervical Transforaminal Epidural Injection with dexamethasone sodium phosphate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 33, "start_date": "2018-10-23", "completion_date": "2023-12-07", "has_results": true, "last_update_posted_date": "2024-04-10", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT04544683" }, { "nct_id": "NCT04341441", "title": "Will Hydroxychloroquine Impede or Prevent COVID-19", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "COVID-19", "Coronavirus", "Coronavirus Infections", "SARS-CoV 2" ], "interventions": [ { "name": "Hydroxychloroquine - Daily Dosing", "type": "DRUG" }, { "name": "Hydroxychloroquine - Weekly Dosing", "type": "DRUG" }, { "name": "Placebo oral tablet", "type": "OTHER" }, { "name": "Monitoring Visit - Baseline", "type": "DIAGNOSTIC_TEST" }, { "name": "Monitoring Visit - Week 4", "type": "DIAGNOSTIC_TEST" }, { "name": "Monitoring Visit - Week 8", "type": "DIAGNOSTIC_TEST" }, { "name": "Weekly Assessment", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Henry Ford Health System", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 624, "start_date": "2020-04-07", "completion_date": "2020-12-15", "has_results": true, "last_update_posted_date": "2022-06-21", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04341441" }, { "nct_id": "NCT05339022", "title": "Supportive Care Intervention (ROAR-LCT) for Patients With Stage IIIA, IIIB, and IV Lung Cancer, ROAR-LCT Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Advanced Lung Non-Small Cell Carcinoma", "Advanced Lung Small Cell Carcinoma", "Extensive Stage Lung Small Cell Carcinoma", "Stage IIIA Lung Cancer AJCC v8", "Stage IIIB Lung Cancer AJCC v8", "Stage IV Lung Cancer AJCC v8", "Stage IVA Lung Cancer AJCC v8", "Stage IVB Lung Cancer AJCC v8", "Unresectable Lung Non-Small Cell Carcinoma", "Unresectable Lung Small Cell Carcinoma" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Exercise Intervention", "type": "OTHER" }, { "name": "Physical Therapy", "type": "PROCEDURE" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Relaxation Therapy", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "sponsor": "Ohio State University Comprehensive Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 100, "start_date": "2022-04-14", "completion_date": "2025-10-01", "has_results": false, "last_update_posted_date": "2025-11-21", "last_synced_at": "2026-09-09T10:14:26.137Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05339022" } ] }