{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Patient+research+surveys&page=12", "query": { "intervention": "Patient research surveys", "page": 12 }, "page_size": 10 }, "pagination": { "page": 12, "page_size": 10, "total_count": 384, "total_pages": 39, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Patient+research+surveys&page=13&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Patient+research+surveys&page=11&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-14T15:39:28.955Z", "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": "NCT05583877", "title": "DM-BOOST Para Latinx: a Diabetes Mellitus Program Using Behavioral Economics to Optimize Outreach and Self-management Support With Technology for Latinx Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus, Type 2" ], "interventions": [ { "name": "Diabetes BOOST", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Daniel Amante", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2025-01-29", "completion_date": "2025-10-31", "has_results": false, "last_update_posted_date": "2026-03-03", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 2, "location_summary": "Worcester, Massachusetts", "locations": [ { "city": "Worcester", "state": "Massachusetts" }, { "city": "Worcester", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05583877" }, { "nct_id": "NCT01739686", "title": "Collaborative Care to Alleviate Symptoms and Adjust to Illness in Chronic Heart Failure (CASA) Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Heart Failure" ], "interventions": [ { "name": "CASA Intervention", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Denver Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 317, "start_date": "2012-08", "completion_date": "2015-12", "has_results": false, "last_update_posted_date": "2017-08-01", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 3, "location_summary": "Aurora, Colorado • Denver, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Denver", "state": "Colorado" }, { "city": "Denver", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT01739686" }, { "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": "2026-10-14T15:39:28.955Z", "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": "NCT04291651", "title": "UCSF PANC Cyst Registry", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Pancreatic Cyst", "Pancreatic Neoplasms", "Pancreatic Cancer", "Pancreatic Diseases", "Pancreatic Intraductal Papillary Mucinous Neoplasm", "Intraductal Papillary Mucinous Neoplasm", "Pancreatic Ductal Adenocarcinoma", "Mucinous Cyst" ], "interventions": [ { "name": "Survey", "type": "OTHER" } ], "intervention_types": [ "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": 4000, "start_date": "2019-10-08", "completion_date": "2030-01-01", "has_results": false, "last_update_posted_date": "2026-09-22", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04291651" }, { "nct_id": "NCT04639973", "title": "Early Anatomy Scan for Evaluation of Obese Pregnant Women (EASE-O)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity" ], "interventions": [ { "name": "Group 1 (First trimester ultrasound)", "type": "DIAGNOSTIC_TEST" }, { "name": "Group 2 (Second trimester anatomy ultrasound)", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 128, "start_date": "2021-02-01", "completion_date": "2022-11-21", "has_results": true, "last_update_posted_date": "2024-05-21", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04639973" }, { "nct_id": "NCT03654066", "title": "Botox or Botox With Esophageal Dilation in Patients With Achalasia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Achalasia" ], "interventions": [ { "name": "Botulinum toxin type A", "type": "DRUG" }, { "name": "Endoscope balloon dilator", "type": "DEVICE" }, { "name": "Patient reported outcomes", "type": "OTHER" }, { "name": "Barium esophagram", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DRUG", "DEVICE", "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "Vanderbilt University 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": 9, "start_date": "2019-05-13", "completion_date": "2026-08-01", "has_results": false, "last_update_posted_date": "2026-08-26", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT03654066" }, { "nct_id": "NCT05662462", "title": "Successfully Achieving and Maintaining Euglycemia During Pregnancy for Type 2 Diabetes Through Technology and Coaching", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pre-Gestational Diabetes", "Type2diabetes", "Pregnancy in Diabetic", "Pregnancy, High Risk" ], "interventions": [ { "name": "DEXCOM G7 PRO Continuous Glucose Monitor", "type": "DEVICE" }, { "name": "Patient mHealth app linked to a provider dashboard", "type": "DEVICE" }, { "name": "Care team coaching for medical and social needs (HUB)", "type": "BEHAVIORAL" }, { "name": "Provider dashboard", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "Ohio State University", "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": 124, "start_date": "2024-07-11", "completion_date": "2029-03", "has_results": false, "last_update_posted_date": "2026-06-29", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05662462" }, { "nct_id": "NCT06343831", "title": "Quantitative Assessment of Autologous Fat Transfer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Autologous Fat Grafting" ], "interventions": [ { "name": "2-Dimensional (2-D) Photographs (Visit 1/ Follow up Visit 3-6)", "type": "PROCEDURE" }, { "name": "3-Dimensional (3-D) Photographs (Visit 1- 6)", "type": "PROCEDURE" }, { "name": "Ultrasound Soft Tissue Assessment (Visit 1/ Follow up Visit 4-6)", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging Volume Assessment (Visit 1/ Follow up Visit 4-6)", "type": "PROCEDURE" }, { "name": "BREAST-QTM questionnaire (Visit 1/ Follow up Visit 4-6)", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15, "start_date": "2024-01-25", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-10-13", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 2, "location_summary": "Chicago, Illinois • Houston, Texas", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06343831" }, { "nct_id": "NCT06224205", "title": "Digital Detection of Dementia (D Cubed) Studies: D3", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alzheimer Disease and Related Dementias (ADRD)" ], "interventions": [ { "name": "Passive Digital Marker for screening for ADRD", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 1281, "start_date": "2023-11-08", "completion_date": "2025-11-08", "has_results": false, "last_update_posted_date": "2026-08-03", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 1, "location_summary": "Boca Raton, Florida", "locations": [ { "city": "Boca Raton", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06224205" }, { "nct_id": "NCT03758521", "title": "Natural History Study of Patients With Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Succinic Semialdehyde Dehydrogenase Deficiency" ], "interventions": [ { "name": "Transcranial magnetic stimulation (TMS)", "type": "DEVICE" }, { "name": "Magnetic resonance imaging (MRI)", "type": "DEVICE" }, { "name": "Electroencephalogram (EEG)", "type": "DEVICE" }, { "name": "Bio-specimen Collection", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "Boston Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 55, "start_date": "2019-01-15", "completion_date": "2029-06", "has_results": false, "last_update_posted_date": "2026-01-13", "last_synced_at": "2026-10-14T15:39:28.955Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03758521" } ] }