{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=exercise&page=40", "query": { "intervention": "exercise", "page": 40 }, "page_size": 10 }, "pagination": { "page": 40, "page_size": 10, "total_count": 637, "total_pages": 64, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=exercise&page=41&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=exercise&page=39&page_size=10" }, "source": "local", "last_synced_at": "2026-10-17T04:08:36.203Z", "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": "NCT07871396", "title": "Exercise Training Intensity and Nitrate Supplementation in Post-Menopausal Females on Hormone Therapy", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Menopausal Hormone Therapy", "Postmenopausal Female Patients", "Vasomotor Symptoms" ], "interventions": [ { "name": "Control (No exercise)", "type": "OTHER" }, { "name": "High intensity exercise (HIE)", "type": "OTHER" }, { "name": "Moderate Intensity Exercise (MIE)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Virginia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "45 Years", "maximum_age": "75 Years", "sex": "FEMALE", "summary": "45 Years to 75 Years · Female only" }, "enrollment_count": 24, "start_date": "2026-10-15", "completion_date": "2028-01-30", "has_results": false, "last_update_posted_date": "2026-10-16", "last_synced_at": "2026-10-17T04:08:36.203Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07871396" }, { "nct_id": "NCT07869472", "title": "Post-exercise Blood Pressure With Inorganic Nitrate", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Central Adiposity", "Obese Individuals" ], "interventions": [ { "name": "Beetroot Juice - Active + Exercise", "type": "DIETARY_SUPPLEMENT" }, { "name": "Beetroot Juice - Active + No exercise", "type": "DIETARY_SUPPLEMENT" }, { "name": "Beetroot juice placebo + Exercise", "type": "DIETARY_SUPPLEMENT" }, { "name": "Beetroot juice placebo+ No exercise", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "University of Virginia", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 12, "start_date": "2026-10-15", "completion_date": "2027-03-30", "has_results": false, "last_update_posted_date": "2026-10-09", "last_synced_at": "2026-10-14T06:19:22.325Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07869472" }, { "nct_id": "NCT07832084", "title": "Comparing Different Medication Regimens to Maintaining Weight Loss Among Adults With Obesity Using GLP-1s", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cardiometabolic Health Indicators", "Obesity & Overweight" ], "interventions": [ { "name": "GLP-1 dose reduction", "type": "DRUG" }, { "name": "Lifestyle/nutrition counseling", "type": "BEHAVIORAL" }, { "name": "Maintenance of GLP-1 dose", "type": "DRUG" }, { "name": "Resistance exercise regimen", "type": "BEHAVIORAL" }, { "name": "non-GLP weight loss medication", "type": "DRUG" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "Jing Luo", "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": "2026-11-01", "completion_date": "2028-09-30", "has_results": false, "last_update_posted_date": "2026-10-05", "last_synced_at": "2026-10-14T20:02:29.050Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07832084" }, { "nct_id": "NCT07503093", "title": "Pilot Study of Sensor-Informed Smartphone-based Mental Health Interventions for Mood in Early Psychosis", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anxiety", "Depression", "Psychosis", "Rumination" ], "interventions": [ { "name": "Neutral Control Message", "type": "BEHAVIORAL" }, { "name": "Smartphone-based Mindfulness Exercise", "type": "BEHAVIORAL" }, { "name": "Smartphone-based Psychoeducation", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Mclean Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "18 Years to 50 Years" }, "enrollment_count": 10, "start_date": "2027-01-15", "completion_date": "2027-06-01", "has_results": false, "last_update_posted_date": "2026-10-05", "last_synced_at": "2026-10-15T11:21:26.643Z", "location_count": 1, "location_summary": "Belmont, Massachusetts", "locations": [ { "city": "Belmont", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07503093" }, { "nct_id": "NCT07854678", "title": "Virtual Reality Versus Traditional Exercise on EMG Activity in Postural Malalignment", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Forward Head Posture", "Postural Malalignment", "Rounded Shoulder Posture" ], "interventions": [ { "name": "Active free Exercise", "type": "OTHER" }, { "name": "Virtual reality exercise", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Hofstra University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "18 Years to 35 Years" }, "enrollment_count": 40, "start_date": "2026-10-25", "completion_date": "2027-10-25", "has_results": false, "last_update_posted_date": "2026-10-02", "last_synced_at": "2026-10-15T07:59:48.585Z", "location_count": 1, "location_summary": "Hempstead, New York", "locations": [ { "city": "Hempstead", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07854678" }, { "nct_id": "NCT07106450", "title": "Training Induced Muscle-Adipose EV Communication", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prediabetes" ], "interventions": [ { "name": "Acute Resistance Exercise", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Yuan Wen", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "30 Years to 55 Years" }, "enrollment_count": 40, "start_date": "2026-11", "completion_date": "2028-09-30", "has_results": false, "last_update_posted_date": "2026-10-02", "last_synced_at": "2026-10-14T20:08:34.823Z", "location_count": 1, "location_summary": "Lexington, Kentucky", "locations": [ { "city": "Lexington", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT07106450" }, { "nct_id": "NCT07831928", "title": "Evaluation of an Online, On Demand Multimodal Wellness Program to Reduce Fatigue and Improve Quality of Life in Progressive Multiple Sclerosis.", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Primary Progressive Multiple Sclerosis (PPMS)", "Secondary Progressive Multiple Sclerosis (SPMS)" ], "interventions": [ { "name": "Online wellness course and online exercise platform", "type": "BEHAVIORAL" }, { "name": "Usual Care Group", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "University of Iowa", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "45 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "45 Years to 70 Years" }, "enrollment_count": 118, "start_date": "2026-11-15", "completion_date": "2030-12-15", "has_results": false, "last_update_posted_date": "2026-09-28", "last_synced_at": "2026-10-16T03:27:03.741Z", "location_count": 1, "location_summary": "Iowa City, Iowa", "locations": [ { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT07831928" }, { "nct_id": "NCT06042413", "title": "Prediction and Prevention of Postoperative Mortality and Morbidity", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dementia", "Major Adverse Cardiac and Cerebrovascular Events", "Perioperative Complications", "Postoperative Cognitive Decline", "Postoperative Delirium (POD)", "Postoperative Neurocognitive Disorder" ], "interventions": [ { "name": "Cognitive Training", "type": "BEHAVIORAL" }, { "name": "Daily Exercise", "type": "BEHAVIORAL" }, { "name": "Enhanced Social Support", "type": "BEHAVIORAL" }, { "name": "Intra-operative Standard of Care", "type": "PROCEDURE" }, { "name": "Meditation", "type": "BEHAVIORAL" }, { "name": "Personalized CPC Prehabilitation", "type": "OTHER" }, { "name": "Pre-operative Standard of Care", "type": "PROCEDURE" }, { "name": "Proactive Bundle Interventions", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "PROCEDURE", "OTHER" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 1200, "start_date": "2026-10", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-09-25", "last_synced_at": "2026-10-15T15:10:58.412Z", "location_count": 5, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06042413" }, { "nct_id": "NCT07832422", "title": "Ischemic Compression and Low-Level Laser Therapy for Myofascial Low Back Pain", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Low Back Pain", "Myofascial Pain Syndromes" ], "interventions": [ { "name": "Exercise Program", "type": "OTHER" }, { "name": "Ischemic Compression", "type": "OTHER" }, { "name": "Low-Level Laser Therapy", "type": "DEVICE" }, { "name": "Sham Low-Level Laser Therapy", "type": "DEVICE" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "Nova Southeastern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 45, "start_date": "2026-09", "completion_date": "2027-04", "has_results": false, "last_update_posted_date": "2026-09-22", "last_synced_at": "2026-10-16T23:32:54.857Z", "location_count": 1, "location_summary": "Brooklyn, New York", "locations": [ { "city": "Brooklyn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07832422" }, { "nct_id": "NCT07518888", "title": "Exercise-induced Steroid Changes in Active Surveillance for Prostate Cancer", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prostate Cancer" ], "interventions": [ { "name": "High-Intensity Interval Training (HIIT) Exercise", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "MALE", "summary": "18 Years to 80 Years · Male only" }, "enrollment_count": 49, "start_date": "2026-10", "completion_date": "2028-08", "has_results": false, "last_update_posted_date": "2026-09-21", "last_synced_at": "2026-10-15T16:51:43.271Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07518888" } ] }