{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sleep+Monitoring+Device", "query": { "intervention": "Sleep Monitoring Device" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 391, "total_pages": 40, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sleep+Monitoring+Device&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-03T02:15:33.729Z", "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": "NCT04809285", "title": "Use of the Guardian™ Connect System With Smart Connected Devices", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 1 Diabetes Mellitus" ], "interventions": [ { "name": "Guardian™ Connect system, InPen™ Basal smart cap, smart insulin pens, and InPen™ Diabetes Management app", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Medtronic MiniMed, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "2 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "2 Years to 80 Years" }, "enrollment_count": 217, "start_date": "2021-04-06", "completion_date": "2023-09-29", "has_results": true, "last_update_posted_date": "2024-12-10", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 14, "location_summary": "Little Rock, Arkansas • Loma Linda, California • Newport Beach, California + 11 more", "locations": [ { "city": "Little Rock", "state": "Arkansas" }, { "city": "Loma Linda", "state": "California" }, { "city": "Newport Beach", "state": "California" }, { "city": "Salinas", "state": "California" }, { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04809285" }, { "nct_id": "NCT03567343", "title": "Investigational Test of a New Sleep Supplement", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep", "Mood", "Cognitive Performance" ], "interventions": [ { "name": "Proprietary Spearmint Extract Blend", "type": "DIETARY_SUPPLEMENT" }, { "name": "Control", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "University of Arizona", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "22 Years to 50 Years" }, "enrollment_count": 105, "start_date": "2018-05-18", "completion_date": "2019-10-15", "has_results": true, "last_update_posted_date": "2024-07-18", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 1, "location_summary": "Tucson, Arizona", "locations": [ { "city": "Tucson", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT03567343" }, { "nct_id": "NCT01287208", "title": "Be Fit in Residency: a Randomized Controlled Trial of an Activity Device Among Medicine Residents", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Activity" ], "interventions": [ { "name": "Activity monitor", "type": "DEVICE" }, { "name": "Activity device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "21 Years to 45 Years" }, "enrollment_count": 104, "start_date": "2010-10", "completion_date": "2011-06", "has_results": true, "last_update_posted_date": "2017-12-07", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01287208" }, { "nct_id": "NCT03921840", "title": "A Personalized Behavioral Intervention for Older Adults With Musculoskeletal Pain and Sleep Complaints", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep", "Pain" ], "interventions": [ { "name": "ELDERFITNESS", "type": "BEHAVIORAL" }, { "name": "Control", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "60 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "60 Years to 85 Years" }, "enrollment_count": 27, "start_date": "2019-07-01", "completion_date": "2020-09-10", "has_results": true, "last_update_posted_date": "2022-11-04", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT03921840" }, { "nct_id": "NCT05398276", "title": "Behavioral Exposure for Introceptive Tolerance RCT", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Exercise Sensitivity", "Introceptive Exposure", "Anxiety", "Cardiac Rehabilitation" ], "interventions": [ { "name": "Behavioral Exposure For Introceptive Tolerance", "type": "BEHAVIORAL" }, { "name": "Health Education Control", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rutgers, The State University of New Jersey", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 146, "start_date": "2022-05-03", "completion_date": "2027-02-28", "has_results": false, "last_update_posted_date": "2026-06-12", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 3, "location_summary": "East Brunswick, New Jersey • Hillsborough, New Jersey • New Brunswick, New Jersey", "locations": [ { "city": "East Brunswick", "state": "New Jersey" }, { "city": "Hillsborough", "state": "New Jersey" }, { "city": "New Brunswick", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT05398276" }, { "nct_id": "NCT03322371", "title": "Validation of Frontal EEG to Formal Polysomnography in the ICU", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Deprivation", "Sleep" ], "interventions": [ { "name": "2-lead limited electroencephalography recording", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 44, "start_date": "2017-11-06", "completion_date": "2020-01-01", "has_results": false, "last_update_posted_date": "2021-06-08", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT03322371" }, { "nct_id": "NCT05708222", "title": "Sleep Signal Analysis for Current Major Depressive Episode (SAMDE)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Depressive Episode", "Depression", "Depressive Disorder", "Depressive Disorder, Major", "Depression Mild" ], "interventions": [ { "name": "MEB-001", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Medibio Limited", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "22 Years to 75 Years" }, "enrollment_count": 715, "start_date": "2022-09-01", "completion_date": "2024-07-09", "has_results": false, "last_update_posted_date": "2024-07-11", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 13, "location_summary": "Bradenton, Florida • Blaine, Minnesota • Plymouth, Minnesota + 10 more", "locations": [ { "city": "Bradenton", "state": "Florida" }, { "city": "Blaine", "state": "Minnesota" }, { "city": "Plymouth", "state": "Minnesota" }, { "city": "Clayton", "state": "North Carolina" }, { "city": "Raleigh", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05708222" }, { "nct_id": "NCT04514354", "title": "The Influence of Cardiorespiratory Fitness on Firefighter Cardiovascular Health Under Exercise Conditions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiovascular Diseases", "Post-Exercise Hypotension" ], "interventions": [ { "name": "GEST", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Connecticut", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 21, "start_date": "2015-04", "completion_date": "2016-01", "has_results": false, "last_update_posted_date": "2020-08-14", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 1, "location_summary": "Hartford, Connecticut", "locations": [ { "city": "Hartford", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT04514354" }, { "nct_id": "NCT06516354", "title": "Evaluation of Obstructive Sleep Apnea (OSA) Using Portable Sleep Testing (PST) Devices on an Inpatient Stroke Unit", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obstructive Sleep Apnea" ], "interventions": [ { "name": "Portable sleep apnea screening", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2017-08-01", "completion_date": "2019-03-31", "has_results": false, "last_update_posted_date": "2024-10-04", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 1, "location_summary": "Park Ridge, Illinois", "locations": [ { "city": "Park Ridge", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06516354" }, { "nct_id": "NCT00507923", "title": "Tibetan Yoga in Improving Fatigue and Sleep in Participants With Stage I-III Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anatomic Stage I Breast Cancer AJCC v8", "Anatomic Stage IA Breast Cancer AJCC v8", "Anatomic Stage IB Breast Cancer AJCC v8", "Anatomic Stage II Breast Cancer AJCC v8", "Anatomic Stage IIA Breast Cancer AJCC v8", "Anatomic Stage IIB Breast Cancer AJCC v8", "Anatomic Stage III Breast Cancer AJCC v8", "Anatomic Stage IIIA Breast Cancer AJCC v8", "Anatomic Stage IIIB Breast Cancer AJCC v8", "Anatomic Stage IIIC Breast Cancer AJCC v8", "Prognostic Stage I Breast Cancer AJCC v8", "Prognostic Stage IA Breast Cancer AJCC v8", "Prognostic Stage IB Breast Cancer AJCC v8", "Prognostic Stage II Breast Cancer AJCC v8", "Prognostic Stage IIA Breast Cancer AJCC v8", "Prognostic Stage IIB Breast Cancer AJCC v8", "Prognostic Stage III Breast Cancer AJCC v8", "Prognostic Stage IIIA Breast Cancer AJCC v8", "Prognostic Stage IIIB Breast Cancer AJCC v8", "Prognostic Stage IIIC Breast Cancer AJCC v8", "Breast Cancer" ], "interventions": [ { "name": "Actigraph", "type": "DEVICE" }, { "name": "Best Practice", "type": "OTHER" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Sleep Diary", "type": "OTHER" }, { "name": "Stretching", "type": "OTHER" }, { "name": "Yoga", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "OTHER", "PROCEDURE" ], "sponsor": "M.D. Anderson 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": 452, "start_date": "2006-11-07", "completion_date": "2022-08-11", "has_results": false, "last_update_posted_date": "2023-03-27", "last_synced_at": "2026-09-03T02:15:33.729Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00507923" } ] }