{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=CAN-DO&page=20", "query": { "intervention": "CAN-DO", "page": 20 }, "page_size": 10 }, "pagination": { "page": 20, "page_size": 10, "total_count": 754, "total_pages": 76, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=CAN-DO&page=21&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=CAN-DO&page=19&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-26T09:17:14.986Z", "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": "NCT05208164", "title": "My ESSENCE - A Research Study on Mindfulness for African-Americans With Type 2 Diabetes", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 2 Diabetes", "Sleep", "Stress" ], "interventions": [ { "name": "Mindfunlness Meditation", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Illinois at Chicago", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "21 Years to 75 Years" }, "enrollment_count": 100, "start_date": "2021-04-01", "completion_date": "2025-07-31", "has_results": false, "last_update_posted_date": "2025-03-05", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05208164" }, { "nct_id": "NCT01819909", "title": "Effectiveness Study of Postoperative Rotator Cuff Repair Rehabilitation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Full Thickness Rotator Cuff Tear" ], "interventions": [ { "name": "Postoperative Jackins Exercise Protocol", "type": "PROCEDURE" }, { "name": "Postoperative Pulleys Exercise Protocol", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Orthopedic Institute, Sioux Falls, SD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 53, "start_date": "2008-11", "completion_date": "2016-07", "has_results": false, "last_update_posted_date": "2022-03-02", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 1, "location_summary": "Sioux Falls, South Dakota", "locations": [ { "city": "Sioux Falls", "state": "South Dakota" } ], "official_url": "https://clinicaltrials.gov/study/NCT01819909" }, { "nct_id": "NCT05570604", "title": "Computerized Cognitive Training in Breast Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Cognitive Change", "Cognitive Impairment", "Quality of Life" ], "interventions": [ { "name": "Sweep Seeker", "type": "BEHAVIORAL" }, { "name": "Bird Safari", "type": "BEHAVIORAL" }, { "name": "Jewel Diver", "type": "BEHAVIORAL" }, { "name": "Master Gardener", "type": "BEHAVIORAL" }, { "name": "Road Tour", "type": "BEHAVIORAL" }, { "name": "Computerized Crossword Puzzles", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Ohio State University", "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": 46, "start_date": "2017-05-17", "completion_date": "2020-03-20", "has_results": true, "last_update_posted_date": "2025-04-24", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT05570604" }, { "nct_id": "NCT03952416", "title": "Enhanced Medical Rehabilitation for Spinal Cord Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries" ], "interventions": [ { "name": "Enhanced Medical Rehabilitation (EMR)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Shirley Ryan AbilityLab", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 48, "start_date": "2022-11-15", "completion_date": "2024-07-30", "has_results": false, "last_update_posted_date": "2024-08-05", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03952416" }, { "nct_id": "NCT07096297", "title": "Luspatercept + Darbepoetin in MDS", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "MDS (Myelodysplastic Syndrome)" ], "interventions": [ { "name": "Luspatercept", "type": "DRUG" }, { "name": "Darbeopoetin", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2025-12-16", "completion_date": "2030-08", "has_results": false, "last_update_posted_date": "2026-09-14", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 4, "location_summary": "New Haven, Connecticut • Chicago, Illinois • Columbus, Ohio + 1 more", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Columbus", "state": "Ohio" }, { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07096297" }, { "nct_id": "NCT01794624", "title": "Biobehavioral Pain Management in TMD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Temporomandibular Joint Disorder" ], "interventions": [ { "name": "Cognitive Therapy for Catastrophizing", "type": "BEHAVIORAL" }, { "name": "Behavioral Therapy for Sleep Continuity Disturbance", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "FEMALE", "summary": "18 Years to 60 Years · Female only" }, "enrollment_count": 300, "start_date": "2013-04", "completion_date": "2018-06", "has_results": false, "last_update_posted_date": "2018-07-19", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 2, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" }, { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01794624" }, { "nct_id": "NCT01710943", "title": "Web-based CBT for Recent Veterans Experiencing Problems With Trauma Symptoms or Alcohol/Drug Use", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Post-Traumatic Stress Symptoms", "Problematic Use of Alcohol or Other Drugs" ], "interventions": [ { "name": "Web-based Cognitive Behavioral Treatment", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "National Development and Research Institutes, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 216, "start_date": "2010-09", "completion_date": "2014-06", "has_results": false, "last_update_posted_date": "2012-10-19", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 2, "location_summary": "Buffalo, New York • Syracuse, New York", "locations": [ { "city": "Buffalo", "state": "New York" }, { "city": "Syracuse", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01710943" }, { "nct_id": "NCT01726582", "title": "Pancreas Cancer: Molecular Profiling as a Guide to Therapy Before and After Surgery (\"Personalized Medicine\")", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Pancreatic Adenocarcinoma" ], "interventions": [ { "name": "Milestone 1: Targeted chemotherapy prior to surgery", "type": "DRUG" }, { "name": "Milestone 2: Chemoradiotherapy (cXRT)", "type": "RADIATION" }, { "name": "Milestone 3: Targeted chemotherapy prior to surgery", "type": "DRUG" }, { "name": "Milestone 3: Chemoradiotherapy (cXRT)", "type": "RADIATION" }, { "name": "Milestone 4: standard FOLFIRINOX chemotherapy prior to surgery", "type": "DRUG" }, { "name": "Milestone 4: Chemoradiotherapy (cXRT)", "type": "RADIATION" }, { "name": "Milestone 5: Targeted chemotherapy after surgery", "type": "DRUG" }, { "name": "Milestone 5: Chemoradiotherapy (cXRT)", "type": "RADIATION" }, { "name": "Milestone 6: Gemcitabine after surgery", "type": "DRUG" }, { "name": "Milestone 6: Chemoradiotherapy (cXRT)", "type": "RADIATION" }, { "name": "Milestone 7: Chemoradiotherapy (cXRT)", "type": "RADIATION" }, { "name": "Milestone 8: Targeted chemotherapy after surgery", "type": "DRUG" }, { "name": "Milestone 9: Gemcitabine after surgery", "type": "DRUG" }, { "name": "Milestone 10: No additional therapy after surgery", "type": "OTHER" } ], "intervention_types": [ "DRUG", "RADIATION", "OTHER" ], "sponsor": "Medical College of Wisconsin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 229, "start_date": "2011-11", "completion_date": "2022-04-11", "has_results": true, "last_update_posted_date": "2023-08-14", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 2, "location_summary": "Cincinnati, Ohio • Milwaukee, Wisconsin", "locations": [ { "city": "Cincinnati", "state": "Ohio" }, { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT01726582" }, { "nct_id": "NCT07483333", "title": "Comparative Effectiveness of SPARCS and Unified Protocol for Youth With Chronic Medical Conditions and Trauma-Related Distress", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Trauma Exposure", "Trauma", "Trauma and Stressor Related Disorder", "Mental Health Functioning", "Chronic Medical Conditions", "Chronic Medical Condition", "Chronic Medical Illness", "Posttraumatic Stress Disorder PTSD", "Posttraumatic Stress Disorders", "Posttraumatic Stress Symptoms", "Posttraumatic Stress" ], "interventions": [ { "name": "Structured Psychotherapy for Adolescents Responding to Chronic Stress - Group", "type": "BEHAVIORAL" }, { "name": "Unified Protocol for Transdiagnostic Treatment of Emotional Disorders in Children and Adolescents - Group", "type": "BEHAVIORAL" }, { "name": "Unified Protocol for Transdiagnostic Treatment of Emotional Disorders in Children and Adolescents - Individual", "type": "BEHAVIORAL" }, { "name": "Structured Psychotherapy for Adolescents Responding to Chronic Stress - Individual", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Anthony Vesco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "8 Years to 18 Years" }, "enrollment_count": 400, "start_date": "2026-10", "completion_date": "2029-09-29", "has_results": false, "last_update_posted_date": "2026-09-15", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07483333" }, { "nct_id": "NCT05512052", "title": "Preventing Preterm Birth With a Negative Pressure Cervical Cup: a Feasibility Study", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Preterm Birth", "Cervical Incompetence", "Cervical Insufficiency", "Short Cervix", "Soft Cervix" ], "interventions": [ { "name": "Hannah Cervical Cup (2 mm Delta)", "type": "DEVICE" }, { "name": "Hannah Cervical Cup (4 mm Delta)", "type": "DEVICE" }, { "name": "Hannah Cervical Cup (6 mm Delta)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Galena Innovations, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 40, "start_date": "2023-04", "completion_date": "2024-04", "has_results": false, "last_update_posted_date": "2022-08-26", "last_synced_at": "2026-10-26T09:17:14.986Z", "location_count": 1, "location_summary": "Provo, Utah", "locations": [ { "city": "Provo", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT05512052" } ] }