{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Wearable&page=23", "query": { "intervention": "Wearable", "page": 23 }, "page_size": 10 }, "pagination": { "page": 23, "page_size": 10, "total_count": 1106, "total_pages": 111, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Wearable&page=24&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Wearable&page=22&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-30T13:25:49.352Z", "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": "NCT05795842", "title": "DELTA (Detecting and Predicting Atrial Fibrillation in Post-Stroke Patients)", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Stroke, Ischemic" ], "interventions": [ { "name": "wearable wristband model", "type": "DEVICE" }, { "name": "Samsung Galaxy Watch 6", "type": "OTHER" }, { "name": "Standard of care extended ECG monitoring", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "55 Years", "maximum_age": null, "sex": "ALL", "summary": "55 Years and older" }, "enrollment_count": 500, "start_date": "2023-03-21", "completion_date": "2028-12", "has_results": false, "last_update_posted_date": "2026-01-21", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05795842" }, { "nct_id": "NCT05935241", "title": "mPATH for Low-income Older Adults", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sedentary Time", "Insomnia", "Cognitive Decline" ], "interventions": [ { "name": "mPATH", "type": "BEHAVIORAL" }, { "name": "Attention Control", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 176, "start_date": "2024-05-30", "completion_date": "2029-12-31", "has_results": false, "last_update_posted_date": "2026-04-13", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT05935241" }, { "nct_id": "NCT05360056", "title": "Continuous Glucose Monitoring Following Hospital Discharge", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 2 Diabetes" ], "interventions": [ { "name": "DexCom G6", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Kathleen Dungan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 108, "start_date": "2022-04-26", "completion_date": "2027-01", "has_results": true, "last_update_posted_date": "2026-07-21", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05360056" }, { "nct_id": "NCT03404596", "title": "Applying mHealth to Tobacco-related Health Disparities", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Smoking Cessation" ], "interventions": [ { "name": "Nicotine Patch", "type": "DRUG" }, { "name": "Counseling", "type": "BEHAVIORAL" }, { "name": "Smartphone", "type": "BEHAVIORAL" }, { "name": "AutoSense", "type": "OTHER" } ], "intervention_types": [ "DRUG", "BEHAVIORAL", "OTHER" ], "sponsor": "H. Lee Moffitt Cancer Center and Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2018-07-16", "completion_date": "2020-12-14", "has_results": false, "last_update_posted_date": "2023-05-11", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03404596" }, { "nct_id": "NCT06161454", "title": "Xofluza-Wearables Feasibility-Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Infection, Coronavirus", "Infections", "Influenza", "Transplant", "Infection Viral" ], "interventions": [ { "name": "Baloxavir Marboxil", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Children's Hospital of Philadelphia", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 498, "start_date": "2023-12-14", "completion_date": "2025-04-30", "has_results": false, "last_update_posted_date": "2025-07-11", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06161454" }, { "nct_id": "NCT04450251", "title": "Testing a Wearable Monitor for Fetal Heart Rate Estimation, Fetal Movement and Uterine Activity Detection", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Pregnancy" ], "interventions": [ { "name": "Data Collection", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Owlet Baby Care, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 173, "start_date": "2018-08-29", "completion_date": "2023-05-01", "has_results": false, "last_update_posted_date": "2025-09-22", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Lehi, Utah", "locations": [ { "city": "Lehi", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT04450251" }, { "nct_id": "NCT06618157", "title": "Connectomic Guided DBS for Parkinson's Disease", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Parkinson Disease", "Tremor", "Dyskinesias" ], "interventions": [ { "name": "Cerebellothalamic optimized deep brain stimulation", "type": "DEVICE" }, { "name": "Pallidothalamic optimized deep brain stimulation", "type": "DEVICE" }, { "name": "No deep brain stimulation", "type": "OTHER" }, { "name": "Usual care deep brain stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2026-02-16", "completion_date": "2027-01-29", "has_results": false, "last_update_posted_date": "2026-09-03", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06618157" }, { "nct_id": "NCT06247254", "title": "Telehealth-Enhanced Assessment and Management", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Blood Pressure" ], "interventions": [ { "name": "Intensive Clinic Management", "type": "BEHAVIORAL" }, { "name": "Intensive Tailored Telehealth Management", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "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": 86, "start_date": "2024-11-15", "completion_date": "2028-07", "has_results": false, "last_update_posted_date": "2026-04-13", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06247254" }, { "nct_id": "NCT05128994", "title": "Hand Grasp Function After Spinal Cord Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries" ], "interventions": [ { "name": "User-controlled FES system", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Battelle Memorial Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 5, "start_date": "2022-04-05", "completion_date": "2024-07-31", "has_results": false, "last_update_posted_date": "2024-08-05", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05128994" }, { "nct_id": "NCT04908254", "title": "A Multi-center Randomized Control Cross-over Study to Evaluate the Safety and Effectiveness of the Dayspring Active Wearable Compression Device vs. an Advanced Pneumatic Compression Device for Treating Breast Cancer Related Lymphedema", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lymphedema", "Lymphedema of Upper Arm", "Lymphedema, Breast Cancer" ], "interventions": [ { "name": "Crossover Device (PCD or Dayspring - alternate to first group)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Koya Medical, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2021-06-01", "completion_date": "2021-12-31", "has_results": false, "last_update_posted_date": "2025-12-09", "last_synced_at": "2026-10-30T13:25:49.352Z", "location_count": 2, "location_summary": "Los Altos, California • Morgan Hill, California", "locations": [ { "city": "Los Altos", "state": "California" }, { "city": "Morgan Hill", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04908254" } ] }