{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=High-Risk+Message&page=5", "query": { "intervention": "High-Risk Message", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 257, "total_pages": 26, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=High-Risk+Message&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=High-Risk+Message&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T22:36:26.446Z", "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": "NCT04848051", "title": "Implementing Fit Kit Colorectal Cancer (CRC) Screening in High Risk Populations", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colorectal Cancer" ], "interventions": [ { "name": "CRC screening reminder", "type": "BEHAVIORAL" }, { "name": "CRC Reminder & Short message", "type": "BEHAVIORAL" }, { "name": "CRC Reminder and Navigation Program", "type": "BEHAVIORAL" }, { "name": "CRC Reminder & CRC education", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "50 Years", "maximum_age": "74 Years", "sex": "ALL", "summary": "50 Years to 74 Years" }, "enrollment_count": 3127, "start_date": "2021-10-12", "completion_date": "2022-11-21", "has_results": false, "last_update_posted_date": "2023-03-03", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT04848051" }, { "nct_id": "NCT07124728", "title": "Syntrillo Telehealth Stroke Risk Reduction Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension", "Hypertension (HTN)", "Stroke Prevention", "Cardiovascular Risk Factor" ], "interventions": [ { "name": "Technology-enabled Telehealth Care Plan", "type": "BEHAVIORAL" }, { "name": "Blood Pressure Monitoring Device", "type": "DEVICE" }, { "name": "Tenovi Smart Pillbox", "type": "DEVICE" }, { "name": "Wearable Activity Trackers (Fitbit or Apple Watch)", "type": "DEVICE" }, { "name": "Healthie EHR", "type": "OTHER" }, { "name": "Secure Messaging Platforms (TigerConnect, Weave, AirCall)", "type": "OTHER" }, { "name": "Antihypertensive Medication Management", "type": "DRUG" }, { "name": "Statin Medication Management", "type": "DRUG" }, { "name": "Antiplatelet or Anticoagulant Therapy", "type": "DRUG" }, { "name": "Laboratory Blood Test Collection", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE", "OTHER", "DRUG", "PROCEDURE" ], "sponsor": "Syntrillo, Inc", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": null, "sex": "ALL", "summary": "30 Years and older" }, "enrollment_count": 11, "start_date": "2025-07-30", "completion_date": "2026-07-22", "has_results": false, "last_update_posted_date": "2026-07-30", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07124728" }, { "nct_id": "NCT04456764", "title": "The Sleep and Teamwork in EMS Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Fatigue", "Sleep" ], "interventions": [ { "name": "SaFTiE", "type": "BEHAVIORAL" }, { "name": "Attention Placebo Control", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 708, "start_date": "2020-09-16", "completion_date": "2024-03-31", "has_results": true, "last_update_posted_date": "2025-05-18", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04456764" }, { "nct_id": "NCT07524244", "title": "Ketogenic and Carnivore (Lion) Diets for Inflammatory Bowel Disease and Rheumatoid Arthritis", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Rheumatoid Arthritis (RA)", "Crohn's Disease (CD)", "Ulcerative Colitis (UC)" ], "interventions": [ { "name": "Ketogenic diet", "type": "BEHAVIORAL" }, { "name": "Carnivore (Lion) Diet", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Fuller Research Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 160, "start_date": "2026-02-17", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2026-10-05", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07524244" }, { "nct_id": "NCT01125371", "title": "Computerized Brief Alcohol Intervention (BI) for Binge Drinking HIV At-Risk and Infected Women", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alcohol; Harmful Use", "Binge Drinking", "Risk Behavior", "HIV Infection" ], "interventions": [ { "name": "Computerized brief alcohol intervention + IVR booster calls", "type": "BEHAVIORAL" }, { "name": "Computerized brief alcohol intervention", "type": "BEHAVIORAL" }, { "name": "Attention Control", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "FEMALE", "summary": "18 Years to 90 Years · Female only" }, "enrollment_count": 439, "start_date": "2011-10", "completion_date": "2016-06-07", "has_results": true, "last_update_posted_date": "2022-06-24", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01125371" }, { "nct_id": "NCT02063737", "title": "SleepTrackTXT Feasibility and Pilot Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Fatigue" ], "interventions": [ { "name": "Text-message assessments only", "type": "BEHAVIORAL" }, { "name": "Text-message interventions for high level fatigue", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2014-01", "completion_date": "2014-06", "has_results": true, "last_update_posted_date": "2015-08-05", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02063737" }, { "nct_id": "NCT06057727", "title": "Behavioral Economics to Improve Flu Vaccination Using EHR Nudges", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Behavior, Health", "Flu", "Flu Vaccination" ], "interventions": [ { "name": "Pre-visit patient text messaging", "type": "BEHAVIORAL" }, { "name": "Default pended order", "type": "BEHAVIORAL" }, { "name": "Monthly peer comparison feedback", "type": "BEHAVIORAL" }, { "name": "High risk bidirectional pre-visit text messaging", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 80039, "start_date": "2023-09-25", "completion_date": "2024-05-20", "has_results": true, "last_update_posted_date": "2025-04-27", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 2, "location_summary": "Philadelphia, Pennsylvania • Seattle, Washington", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06057727" }, { "nct_id": "NCT05426070", "title": "Preliminary Efficacy of a Strength Training Intervention on Exercise Adherence and Weight Among Pre-Menopausal Women", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Inactivity", "Obesity" ], "interventions": [ { "name": "Strength training-based exercise", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "40 Years to 50 Years · Female only" }, "enrollment_count": 39, "start_date": "2022-12-30", "completion_date": "2023-12-10", "has_results": false, "last_update_posted_date": "2024-01-08", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05426070" }, { "nct_id": "NCT03232762", "title": "Effects of Diet on Pregnancy Outcome and Child Obesity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pregnancy Related", "Diet Modification", "Obesity", "Hypertension", "Pre-Eclampsia", "Blood Pressure", "Breast Feeding", "Birth Weight" ], "interventions": [ { "name": "Refined Grains", "type": "DIETARY_SUPPLEMENT" }, { "name": "Whole Grains", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 303, "start_date": "2017-10-03", "completion_date": "2019-08-22", "has_results": false, "last_update_posted_date": "2019-11-13", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03232762" }, { "nct_id": "NCT07857200", "title": "The Use of Risk Prediction to Identify Patients at Risk for Chronic Kidney Disease: Patient and Provider Interventions for Patients at High Risk for Chronic Kidney Disease", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "CKD - Chronic Kidney Disease" ], "interventions": [ { "name": "Letter Intervention", "type": "OTHER" }, { "name": "Letter + Phone Call Intervention:", "type": "OTHER" }, { "name": "Augmented usual care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Kaiser Permanente", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 1500, "start_date": "2026-08-20", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-10-05", "last_synced_at": "2026-10-23T22:36:26.446Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT07857200" } ] }