{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=General+Educational+Materials", "query": { "intervention": "General Educational Materials" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 88, "total_pages": 9, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=General+Educational+Materials&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-06T05:26:02.561Z", "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": "NCT05038215", "title": "Increasing Adherence to Oral Appliance Therapy for Obstructive Sleep Apnea", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obstructive Sleep Apnea", "Adherence, Patient" ], "interventions": [ { "name": "adherence promotion techniques", "type": "BEHAVIORAL" }, { "name": "Routine Care", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "PROCEDURE" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2017-12-05", "completion_date": "2022-09-01", "has_results": false, "last_update_posted_date": "2024-05-03", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05038215" }, { "nct_id": "NCT05343468", "title": "Life Skills Improved in Children With Down Syndrome After Using Assistive Technology", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Down Syndrome", "Adaptive Behavior", "Quality of Life" ], "interventions": [ { "name": "The MapHabit System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "MapHabit, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "7 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "7 Years to 17 Years" }, "enrollment_count": 26, "start_date": "2020-09-20", "completion_date": "2021-08-05", "has_results": false, "last_update_posted_date": "2023-02-24", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05343468" }, { "nct_id": "NCT02368132", "title": "Delivery Models of Caregiver Support and Education", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dementia" ], "interventions": [ { "name": "Group Delivered TEP", "type": "BEHAVIORAL" }, { "name": "Individual Delivered TEP", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 319, "start_date": "2016-05-13", "completion_date": "2021-02-24", "has_results": true, "last_update_posted_date": "2023-07-27", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 2, "location_summary": "Buffalo, New York • Philadelphia, Pennsylvania", "locations": [ { "city": "Buffalo", "state": "New York" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02368132" }, { "nct_id": "NCT05059132", "title": "Inspiratory Muscle Training and Behavioral Support to Alleviate Dyspnea and Promote Walking in Lung Cancer Survivors: A Pilot Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lung Neoplasm" ], "interventions": [ { "name": "Tele-rehabilitation", "type": "BEHAVIORAL" }, { "name": "Education only", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Kaiser Permanente", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 31, "start_date": "2022-01-10", "completion_date": "2022-12-31", "has_results": false, "last_update_posted_date": "2023-12-13", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT05059132" }, { "nct_id": "NCT01155011", "title": "Multilevel Intervention for Physical Activity in Retirement Communities", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Activity", "Blood Pressure", "Physical Functioning", "Quality of Life", "Sedentary" ], "interventions": [ { "name": "Physical Activity", "type": "BEHAVIORAL" }, { "name": "Group educational sessions", "type": "BEHAVIORAL" }, { "name": "Phone counseling call", "type": "BEHAVIORAL" }, { "name": "Peer Mentoring", "type": "BEHAVIORAL" }, { "name": "Policy Change", "type": "BEHAVIORAL" }, { "name": "Support", "type": "BEHAVIORAL" }, { "name": "Tailored environmental resources", "type": "BEHAVIORAL" }, { "name": "Health check phone call", "type": "BEHAVIORAL" }, { "name": "Pedometer", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 307, "start_date": "2011-01", "completion_date": "2014-07", "has_results": true, "last_update_posted_date": "2017-08-31", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01155011" }, { "nct_id": "NCT00929838", "title": "Telephone Delivered Behavioral Skills Intervention for Blacks With T2DM", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus, Type 2", "Diabetes Mellitus, Adult-Onset", "Diabetes Mellitus, Non-Insulin-Dependent", "Diabetes Mellitus, Noninsulin Dependent", "Diabetes Mellitus, Type II" ], "interventions": [ { "name": "Diabetes Knowledge/Information", "type": "BEHAVIORAL" }, { "name": "Motivation/Behavioral Skills", "type": "BEHAVIORAL" }, { "name": "Combined Intervention", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "State University of New York at Buffalo", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 256, "start_date": "2008-08", "completion_date": "2016-06", "has_results": true, "last_update_posted_date": "2024-07-12", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00929838" }, { "nct_id": "NCT02390245", "title": "Philadelphia Telemedicine Glaucoma Detection and Follow-Up Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glaucoma", "Glaucoma Suspect", "Diabetic Retinopathy", "Ocular Hypertension", "Cataract", "Branch Retinal Vein Occlusion", "Branch Retinal Arterial Occlusion", "Central Retinal Vein Occlusion", "Central Retinal Artery Occlusion", "Epi-retinal Membrane", "Macular Degeneration", "Drusen", "Loss of Vision" ], "interventions": [ { "name": "Free Eye Screenings", "type": "OTHER" }, { "name": "Enhanced Intervention", "type": "OTHER" }, { "name": "Usual Care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Wills Eye", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 906, "start_date": "2014-09", "completion_date": "2020-08", "has_results": true, "last_update_posted_date": "2022-08-22", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02390245" }, { "nct_id": "NCT07333482", "title": "Flourish: Exploring the Early Infant Gut Microbiome", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Microbiota", "Gut Microbiome", "Eczema", "Microbiome" ], "interventions": [ { "name": "Tailored Recommendations", "type": "DIETARY_SUPPLEMENT" }, { "name": "Consult Call", "type": "BEHAVIORAL" }, { "name": "Educational Email Series", "type": "BEHAVIORAL" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "BEHAVIORAL" ], "sponsor": "Seeding Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "0 Months", "maximum_age": "3 Months", "sex": "ALL", "summary": "0 Months to 3 Months" }, "enrollment_count": 250, "start_date": "2026-01-31", "completion_date": "2028-09", "has_results": false, "last_update_posted_date": "2026-02-24", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07333482" }, { "nct_id": "NCT02451735", "title": "Genetic Counseling for Breast Cancer Survivors (GC for BC)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Video and Booklet", "type": "BEHAVIORAL" }, { "name": "Factsheet", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "H. Lee Moffitt Cancer Center and Research Institute", "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": 157, "start_date": "2012-07-27", "completion_date": "2019-07-12", "has_results": false, "last_update_posted_date": "2019-11-08", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02451735" }, { "nct_id": "NCT00819208", "title": "Health Education Materials With/Out a Physical Activity Program for Patients Who Have Undergone Treatment for High-Risk Stage II or Stage III Colon Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anxiety Disorder", "Cognitive/Functional Effects", "Colorectal Cancer", "Depression", "Fatigue", "Psychosocial Effects of Cancer and Its Treatment", "Sleep Disorders", "Excercise" ], "interventions": [ { "name": "exercise intervention", "type": "BEHAVIORAL" }, { "name": "counseling intervention", "type": "OTHER" }, { "name": "Educational Intervention", "type": "OTHER" }, { "name": "laboratory biomarker analysis", "type": "OTHER" }, { "name": "questionnaire administration", "type": "OTHER" }, { "name": "study of socioeconomic and demographic variables", "type": "OTHER" }, { "name": "fatigue assessment and management", "type": "PROCEDURE" }, { "name": "quality-of-life assessment", "type": "PROCEDURE" }, { "name": "Fitness testing", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "PROCEDURE" ], "sponsor": "Canadian Cancer Trials Group", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 889, "start_date": "2009-06-02", "completion_date": "2026-03-17", "has_results": true, "last_update_posted_date": "2026-04-24", "last_synced_at": "2026-09-06T05:26:02.561Z", "location_count": 3, "location_summary": "Detroit, Michigan • Lebanon, New Hampshire • Chapel Hill, North Carolina", "locations": [ { "city": "Detroit", "state": "Michigan" }, { "city": "Lebanon", "state": "New Hampshire" }, { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00819208" } ] }