{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Activity+scheduling", "query": { "intervention": "Activity scheduling" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 1308, "total_pages": 131, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Activity+scheduling&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-05T12:42:16.934Z", "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": "NCT03069222", "title": "Longitudinal Assessment of Spinal Cord Structural Plasticity Using DTI in SCI Patients", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Spinal Cord Injuries" ], "interventions": [ { "name": "Standard Rehabilitative Treatment", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Kessler Foundation", "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": 19, "start_date": "2016-04-01", "completion_date": "2020-03-31", "has_results": false, "last_update_posted_date": "2020-09-11", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 1, "location_summary": "West Orange, New Jersey", "locations": [ { "city": "West Orange", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT03069222" }, { "nct_id": "NCT02090634", "title": "Texting to Improve Adherence in HIV+ With Bipolar Disorder", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Disease", "Bipolar Disorder" ], "interventions": [ { "name": "Psychoeducation", "type": "BEHAVIORAL" }, { "name": "individualized Texting for Adherence Building (iTAB)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 58, "start_date": "2010-04", "completion_date": "2012-03", "has_results": true, "last_update_posted_date": "2021-08-27", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02090634" }, { "nct_id": "NCT03272438", "title": "Schedule Intervention to Increase Sustainable Walking Activity in Midlife Working Adults", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Activity" ], "interventions": [ { "name": "Accelerometer", "type": "DEVICE" }, { "name": "Step goal", "type": "BEHAVIORAL" }, { "name": "Consistent contexts", "type": "BEHAVIORAL" }, { "name": "Inconsistent contexts", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "Brandeis University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "40 Years to 65 Years" }, "enrollment_count": 149, "start_date": "2018-04-13", "completion_date": "2019-07-24", "has_results": false, "last_update_posted_date": "2025-02-17", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 1, "location_summary": "Waltham, Massachusetts", "locations": [ { "city": "Waltham", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03272438" }, { "nct_id": "NCT01306032", "title": "Phase II ABT-888 With Cyclophosphamide", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Ovarian Cancer", "Primary Peritoneal Cancer", "Serous Carcinoma Cancer", "Triple-Negative Breast Cancer", "Fallopian Tube Cancer" ], "interventions": [ { "name": "ABT-888", "type": "DRUG" }, { "name": "Cyclophosphamide", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 124, "start_date": "2011-01-12", "completion_date": "2016-12-15", "has_results": true, "last_update_posted_date": "2017-04-26", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 9, "location_summary": "Davis, California • Tampa, Florida • Chicago, Illinois + 6 more", "locations": [ { "city": "Davis", "state": "California" }, { "city": "Tampa", "state": "Florida" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Bethesda", "state": "Maryland" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT01306032" }, { "nct_id": "NCT06979336", "title": "A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics (PK) of RO7837195 in Participants With Moderately to Severely Active Ulcerative Colitis (UC)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Ulcerative Colitis" ], "interventions": [ { "name": "RO7837195", "type": "DRUG" }, { "name": "RO7837195 Matched Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Genentech, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 224, "start_date": "2025-09-29", "completion_date": "2028-10-31", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 8, "location_summary": "Lancaster, California • San Diego, California • Colorado Springs, Colorado + 5 more", "locations": [ { "city": "Lancaster", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "Colorado Springs", "state": "Colorado" }, { "city": "Kissimmee", "state": "Florida" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06979336" }, { "nct_id": "NCT05494385", "title": "Effect of Perioperative Gabapentin on Postoperative Opioid Requirements", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "Preoperative Gabapentin/Postoperative Placebo", "type": "DRUG" }, { "name": "Preoperative Gabapentin/Postoperative Gabapentin", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Indiana 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": 114, "start_date": "2021-07-27", "completion_date": "2023-07-05", "has_results": true, "last_update_posted_date": "2024-10-23", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT05494385" }, { "nct_id": "NCT07416552", "title": "A Study to Investigate CEA-PRIT 2.0 in Participants With Metastatic Colorectal Cancer (mCRC)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Metastatic Colorectal Cancer" ], "interventions": [ { "name": "SPLIT Abs", "type": "DRUG" }, { "name": "203Pb-DOTAM", "type": "DRUG" }, { "name": "212Pb-DOTAM", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Hoffmann-La Roche", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 180, "start_date": "2026-09-08", "completion_date": "2034-02-12", "has_results": false, "last_update_posted_date": "2026-09-04", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 3, "location_summary": "Omaha, Nebraska • Houston, Texas • Madison, Wisconsin", "locations": [ { "city": "Omaha", "state": "Nebraska" }, { "city": "Houston", "state": "Texas" }, { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT07416552" }, { "nct_id": "NCT06891638", "title": "Enhancing Reading Recovery in Aphasia With tDCS and Phonomotor Therapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Aphasia" ], "interventions": [ { "name": "Schedule of tDCS administration", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Kessler Foundation", "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": 6, "start_date": "2025-05-12", "completion_date": "2026-02-14", "has_results": false, "last_update_posted_date": "2026-05-08", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 2, "location_summary": "West Orange, New Jersey • Milwaukee, Wisconsin", "locations": [ { "city": "West Orange", "state": "New Jersey" }, { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT06891638" }, { "nct_id": "NCT04793685", "title": "Prazosin for Alcohol Use Disorder With Withdrawal Symptoms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Alcohol Withdrawal" ], "interventions": [ { "name": "Prazosin", "type": "DRUG" }, { "name": "12-Step Facilitation with Relapse Prevention and Contingency Management", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 150, "start_date": "2021-07-01", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2025-12-11", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT04793685" }, { "nct_id": "NCT04095650", "title": "A New Model to Reach Vulnerable Older Adults With Pain Self-management Support", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Pain" ], "interventions": [ { "name": "STEPS (Seniors using Technology to Engage in Pain Self-management)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 38, "start_date": "2019-09-20", "completion_date": "2020-05-14", "has_results": false, "last_update_posted_date": "2021-01-06", "last_synced_at": "2026-09-05T12:42:16.934Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04095650" } ] }