{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Text+Message+Arm+Intervention&page=23", "query": { "intervention": "Text Message Arm Intervention", "page": 23 }, "page_size": 10 }, "pagination": { "page": 23, "page_size": 10, "total_count": 588, "total_pages": 59, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Text+Message+Arm+Intervention&page=24&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Text+Message+Arm+Intervention&page=22&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-31T12:32:02.188Z", "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": "NCT07226609", "title": "A Dietary Study for People With Multiple Myeloma", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Multiple Myeloma" ], "interventions": [ { "name": "nutrition counseling and coaching", "type": "OTHER" }, { "name": "dietary guidelines, research dietitian visit", "type": "OTHER" }, { "name": "Questionnaires", "type": "BEHAVIORAL" }, { "name": "Frozen pre-prepared meals", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 220, "start_date": "2025-11-04", "completion_date": "2028-11", "has_results": false, "last_update_posted_date": "2026-05-05", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 7, "location_summary": "Basking Ridge, New Jersey • Middletown, New Jersey • Montvale, New Jersey + 4 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Middletown", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07226609" }, { "nct_id": "NCT07485335", "title": "A Bundled Intervention to End Opioid Overdoses", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Use Disorder", "Opioid Overdose" ], "interventions": [ { "name": "Bundled intervention (Experimental)", "type": "OTHER" }, { "name": "control group", "type": "OTHER" }, { "name": "Buprenorphine (Experimental)", "type": "DRUG" }, { "name": "Scheduled Peer Support Specialist (Experimental)", "type": "BEHAVIORAL" }, { "name": "Telemedicine Buprenorphine Treatment", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DRUG", "BEHAVIORAL" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": null, "sex": "ALL", "summary": "19 Years and older" }, "enrollment_count": 160, "start_date": "2026-09-07", "completion_date": "2030-09-30", "has_results": false, "last_update_posted_date": "2026-10-02", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT07485335" }, { "nct_id": "NCT03980743", "title": "Interactive Obesity Treatment Approach for Obesity Prevention in Adults With Early Serious Mental Illness: iOTA-SMI", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity", "Overweight", "Severe Mental Disorder" ], "interventions": [ { "name": "iOTA text messaging intervention", "type": "BEHAVIORAL" }, { "name": "Health Education text messaging intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 51, "start_date": "2020-07-15", "completion_date": "2022-05-31", "has_results": true, "last_update_posted_date": "2024-10-26", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 2, "location_summary": "Miami, Florida • St Louis, Missouri", "locations": [ { "city": "Miami", "state": "Florida" }, { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03980743" }, { "nct_id": "NCT03367923", "title": "Health and Recovery Program in Increasing Physical Activity Level in Stage IA-IIIA Endometrial Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Cancer Survivor", "Endometrial Carcinoma", "Stage I Uterine Corpus Cancer AJCC v7", "Stage IA Uterine Corpus Cancer AJCC v7", "Stage IB Uterine Corpus Cancer AJCC v7", "Stage II Uterine Corpus Cancer AJCC v7", "Stage IIIA Uterine Corpus Cancer AJCC v7" ], "interventions": [ { "name": "Communication Intervention", "type": "OTHER" }, { "name": "Counseling", "type": "OTHER" }, { "name": "Fitbit tracker", "type": "OTHER" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Telephone-Based Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 47, "start_date": "2017-12-01", "completion_date": "2020-03-25", "has_results": false, "last_update_posted_date": "2023-11-28", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 2, "location_summary": "Palo Alto, California • San Jose, California", "locations": [ { "city": "Palo Alto", "state": "California" }, { "city": "San Jose", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03367923" }, { "nct_id": "NCT02466061", "title": "TREC Lifestyle Beyond Cancer Study in Endometrial Cancer Survivors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Endometrial Cancer" ], "interventions": [ { "name": "Telemedicine Weight Management plus Wi-Fi Scale (Arm A)", "type": "BEHAVIORAL" }, { "name": "Text for Diet (Text4Diet) Group (Arm B)", "type": "BEHAVIORAL" }, { "name": "Enhanced Usual Care Group (Arm C)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Fred Hutchinson Cancer Center", "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": 207, "start_date": "2014-07", "completion_date": "2016-06", "has_results": false, "last_update_posted_date": "2016-06-02", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 3, "location_summary": "Boston, Massachusetts • St Louis, Missouri • Philadelphia, Pennsylvania", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "St Louis", "state": "Missouri" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02466061" }, { "nct_id": "NCT07805083", "title": "Community Enhanced Virtual Informed Consent", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hematopoietic and Lymphatic System Neoplasm", "Malignant Solid Neoplasm" ], "interventions": [ { "name": "Educational Cancer Intervention", "type": "BEHAVIORAL" }, { "name": "ICF Text Version 1", "type": "OTHER" }, { "name": "ICF Text Version 2", "type": "OTHER" }, { "name": "ICF Video Version 1", "type": "OTHER" }, { "name": "ICF Video Version 2", "type": "OTHER" }, { "name": "ICF Video Version 3", "type": "OTHER" }, { "name": "ICF Video Version 4", "type": "OTHER" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 600, "start_date": "2026-07-21", "completion_date": "2029-07-20", "has_results": false, "last_update_posted_date": "2026-09-08", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07805083" }, { "nct_id": "NCT03344796", "title": "UV Exposure Assessed With Wearable Sensor and Sun Protection", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sunburn, Erythema", "Sun Protection" ], "interventions": [ { "name": "Goal attainment", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 164, "start_date": "2018-06-30", "completion_date": "2020-09-30", "has_results": true, "last_update_posted_date": "2023-07-27", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03344796" }, { "nct_id": "NCT04525222", "title": "mHealth Mood Management Tool (Actify) to Improve Population-Level Smoking Cessation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Cigarette Smoking-Related Carcinoma" ], "interventions": [ { "name": "Health Promotion and Education", "type": "OTHER" }, { "name": "Smoking Cessation Intervention (Actify app)", "type": "BEHAVIORAL" }, { "name": "Smoking Cessation Intervention (Current Standard Care app)", "type": "BEHAVIORAL" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Fred Hutchinson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 242, "start_date": "2022-05-09", "completion_date": "2023-04-12", "has_results": true, "last_update_posted_date": "2024-03-07", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT04525222" }, { "nct_id": "NCT06919445", "title": "Novel Mobile Resource for Food Insecurity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Food Insecurity" ], "interventions": [ { "name": "'Text Connect' text messages", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 608, "start_date": "2025-03-03", "completion_date": "2026-01-09", "has_results": false, "last_update_posted_date": "2026-01-13", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT06919445" }, { "nct_id": "NCT05551702", "title": "Treating Depression With Text Messaging", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Moderate Depression" ], "interventions": [ { "name": "CBT-txt", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "The University of Tennessee, Knoxville", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "18 Years to 25 Years" }, "enrollment_count": 103, "start_date": "2022-07-06", "completion_date": "2025-01-08", "has_results": false, "last_update_posted_date": "2025-03-28", "last_synced_at": "2026-10-31T12:32:02.188Z", "location_count": 1, "location_summary": "Knoxville, Tennessee", "locations": [ { "city": "Knoxville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT05551702" } ] }